CN107167605B

CN107167605B - For detecting the antibody and kit of CD147 in serum

Info

Publication number: CN107167605B
Application number: CN201710191417.4A
Authority: CN
Inventors: 马杰; 吴云
Original assignee: Individual
Current assignee: Individual
Priority date: 2017-03-28
Filing date: 2017-03-28
Publication date: 2019-04-23
Anticipated expiration: 2037-03-28
Also published as: CN107167605A

Abstract

The present invention relates to serum antigen detection techniques, and in particular to a kind of for detecting the antibody and kit of CD147 in serum.There is provided the antibody pair for detecting liver cancer marker CD147 in test serum, which is characterized in that be made of first antibody and secondary antibody；The first antibody is secreted as coated antibody by the hybridoma that deposit number is CGMCC NO:13587；The secondary antibody is secreted as detection antibody by the hybridoma that deposit number is CGMCC NO:13588.The antibody can uninterruptedly detect CD147 in serum simultaneously with the antibody combined use of other markers to high specificity；High sensitivity, can be detected concentration down to the CD147 of 64pg/ml, being capable of CD147 albumen in accurate quantitative analysis serum.

Description

For detecting the antibody and kit of CD147 in serum

Technical field

The present invention relates to serum antigen detection techniques, and in particular to a kind of for detecting the antibody of CD147 and examination in serum Agent box.

Background technique

Disease incidence of the cancer in the whole world is in rising trend.On 2 3rd, 2014, " the global cancer that the World Health Organization delivers Report 2014 " it shows, the newly-increased cases of cancer height of China ranks first in the world, and wherein the new cases of liver cancer and death toll are equal It occupies first place in the world.Hepatocellular carcinoma (hepatocellularcarcinoma, HCC) is one of most common malignant tumour in the whole world, China is hepatitis B big country, and onset of liver cancer rate accounts for the 55% of global sum.Clinically the diagnosis of liver cancer is mainly detected by serum Alpha-fetoprotein (Alpha-fetoprotein, AFP), B ultrasound find perfused rat liver model, and then CT and MRI is checked.However AFP is positive Rate about 60~70%, and not all hepatocellular carcinoma all secretes a large amount of AFP, about 40% early primary hepatocarcinoma and 15%~ The serum afp of 20% late primary liver cancer patient is normal, therefore only still has the possibility failed to pinpoint a disease in diagnosis by AFP diagnosing liver cancer, Clinical 80% patient is caused to belong to middle and advanced stage when making a definite diagnosis.Mid and late liver cancer is substantially without effective treatment method, to hepatitis B, cirrhosis Equal people at highest risk carry out the screening of hepatic carcinoma marker and early diagnosis is to solve the most effective measure of liver cancer high mortality.

CD147 most has found early in tumor cell surface.Biswas etc. is studies have shown that the CD147 of tumor cell surface can be with The fibroblasts to secrete extracellular matrix metalloproteinases of induced proximity, and it is named as extracellular matrix metalloprotein The enzyme induction factor.Wang etc. is the study found that the positive expression rate (73.53%) of the CD147 in tumor tissues is apparently higher than by cancer It organizes (13.58%).HAb18G/CD147 wide expression in liver cancer cell lines such as Hep-G2, SMCC-7721, BEL7402, but It is not expressed in L-02 mankind's normal liver cell system, and HAb18G/CD147 is positioned at the tumor cell membrane of 74.0% liver cancer patient. In recent years there is scholar's discovery, serum soluble CD147 is more sensitive compared with Serum AFP in terms of the early diagnosis of liver cancer, by serum CD147 is expected to further increase the sensibility of hepatocarcinoma early diagnosis in conjunction with Serum AFP.

Luminex Suspension array technique is a kind of Luminex company, the U.S. more function that mid-term is developed in the 1990s The liquid-phase chip analysis platform of energy, also referred to as liquid chip.It organically incorporates coloured microballoon, laser technology, newest height The fluorescence-encoded micro-beads of speed digital signal processing and computer technology, application are anti-with the specificity for different target molecule Body, different microballoons can be freely combined, and can be detected simultaneously in one 25-50 microlitres of sample and be for up to 100 kinds of differences Detection project, there is repeatability and stability is good, high-throughput, Testing index can flexible choice, and highly sensitive and high letter Make an uproar than many advantages, such as, the analysis of antigen albuminoid and the quantitative analysis of major disease antigen markers suitable for blood plasma, It is the medicine being of great significance an auxiliary detection means.Compared with traditional solid phase chip, solid phase chip is overcome big Interference when Molecular Detection by surface tension, three-dimensional effect etc. to kinetics makes the stability and repeatability of testing result It is greatly improved.

Therefore, CD147 specific antibody is obtained, CD147 content in serum is carried out using Luminex Suspension array technique Detection, it will help improve the recall rate of early liver cancer.

Summary of the invention

In order to improve the recall rate of early liver cancer, the present invention is provided to detect the antibody and kit of CD147 in serum, Its high specificity, high sensitivity can accurately detect the content of CD147 in serum.

Claimed technical solution is as follows:

It is used to prepare the antigen protein of the antibody of anti-CD147, which is characterized in that its amino acid sequence such as SEQ ID NO.9 It is shown.

Encode the gene of the antigen protein, which is characterized in that its nucleotide sequence is as shown in SEQ ID NO.10.

For detecting the monoclonal antibody of liver cancer marker CD147 in test serum, which is characterized in that be by deposit number The hybridoma of CGMCC NO:13588 is secreted.

Secrete the hybridoma of the monoclonal antibody, which is characterized in that its deposit number is CGMCC NO:13588.

For detecting the antibody pair of liver cancer marker CD147 in test serum, which is characterized in that by first antibody and second Antibody composition；The first antibody is as coated antibody, by the hybridoma point that deposit number is CGMCC NO:13587 It secretes；The secondary antibody is secreted as detection antibody by the hybridoma that deposit number is CGMCC NO:13588.

Kit for hepatocarcinoma early diagnosis, which is characterized in that including the monoclonal antibody or the antibody pair, with And the common reagent for immune detection.

The kit, which is characterized in that including the antibody pair, the first antibody and magnetic bead are coupled, and described second Antibody biotin labeling, the common reagent for immune detection are streptavidin-phycoerythrin.

The kit, which is characterized in that further include the standard items of CD147 and/or made with the standard items of the CD147 Standard curve or linear regression equation specification.

Any kit, which is characterized in that further include antibody, the anti-Gorky's glycoprotein 73 of anti-alpha-fetoprotein Antibody, the antibody of the antibody of anti-alpha-L-fucosidase and/or anti-vascular endothelial growth factor and its corresponding immune detection Reagent.

The kit, which is characterized in that further include alpha-fetoprotein, Gorky's glycoprotein 73, alpha-L-fucosidase and/ Or the standard items of vascular endothelial growth factor, and/or with alpha-fetoprotein, Gorky's glycoprotein 73, alpha-L-fucosidase and/ Or the standard curve or linear regression equation specification of the standard items production of vascular endothelial growth factor.

The present invention is using DNA Star sequence analysis software to the amino acid sequence of liver cancer serum marker CD147 (protein ID:BAC76828.1) is analyzed, and the antigenicity of protein sequence, specificity, protein expression and pure are comprehensively considered That changes is ease, chooses the peptide fragment of 25-177aa as antigen, amino acid sequence as shown in SEQ ID NO.9, compile by gene Code sequence is as shown in SEQ ID NO.10.

Antigen protein and immune mouse are obtained by the method for albumen pronucleus expression, filtering out being capable of specific bond CD147 Monoclonal antibody, and by ELISA double antibodies sandwich experiment the monoclonal antibody of acquisition is matched, having screened can For the antibody pair of change of serum C D147 quantitative detection, it is made of first antibody (coated antibody) and secondary antibody (detection antibody), Its hybridoma deposit number is CGMCC NO:13587 and CGMCC NO:13588 respectively.The antibody is to high specificity (CD147 in serum can be uninterruptedly detected simultaneously with the antibody combined use of other markers, see that embodiment 4 is remembered Carry), high sensitivity (can be detected concentration down to 64pg/ml CD147, recorded in embodiment 4), being capable of accurate quantitative analysis blood CD147 albumen in clear.

Kit of the invention can also include removing alpha-fetoprotein, Gorky's glycoprotein 73, alpha-L-fucosidase, blood Other tumor markers except endothelial tube growth factor and extracellular matrix metalloproteinase CD147 it is special Property antibody and its corresponding immunologic function test reagent.

Using antibody pair or kit of the invention, in conjunction with Luminex technology, the immunological technique and mark of double antibodies sandwich Directrix curve realizes the quantitative detection of CD147 in serum.The testing principle of this method is: will be coupled the magnetic bead of first antibody 4 DEG C of the test serum sample overnight incubations with after dilution, form antigen-specific antibodies compound, are washed away with washing buffer Unbonded antigen；The secondary antibody of biotin labeling is added, it is compound to form specific antibody-antigen-antibody for incubation at room temperature Object washes away unbonded antibody with washing buffer；It is added streptavidin-phycoerythrin (SAPE), is incubated at room temperature, formed Antibody-antigene-antibody-biotin-SAPE compound, unbonded SAPE is washed away with washing buffer；Measurement buffer is added It is placed on reading MFI value in liquid phase suspension chip system；Finally MFI value is substituted into the equation of standard curve and calculates sample The concentration of CD147 in product, the actual concentrations of CD147 are obtained multiplied by the extension rate of blood serum sample.

Compared with common detection methods ELISA, method of the invention have the advantages that it is quick, sensitive, and can be one Other liver cancer related neoplasms markers, such as AFP, AFP-L3, GP73, AFU, VEGF etc. are detected in a reaction system simultaneously.Benefit With Luminex liquid microarrays technology, according to the actual needs of diagnosis, antithesis is associated with the glimmering of different tumor markers specific antibodies Pumped FIR laser microballoon is freely combined, and primary experiment can be completed at the same time the quantitative analysis of a variety of liver cancer related neoplasms markers, It has the advantage that (1) one-time detection minimum 10ul of blood plasma dosage, 6 kinds of plasma proteins can be detected simultaneously, greatly reduced Blood plasma dosage, time saving and energy saving, testing cost is low；(2) liquid-phase chip technology reaction system is conducive to keep under liquid phase environment The activity of large biological molecule, so that reaction system is more stable, testing result is relatively reliable accurate；(3) liver in plasma sample Cancer related neoplasms marker AFP, AFP-L3, GP73, AFU, VEGF, CD147 albumen joint-detection makes Diagnostic Value of Several Serum Tumor Markers Between correlation analysis it is more accurate, the diagnosis of liver cancer early stage can be improved, to formulate therapeutic scheme in time, extend Patient vitals.

Biological deposits information

Preservation mechanism: China Committee for Culture Collection of Microorganisms's common micro-organisms center

Address: Yard 1, BeiChen xi Road, Chaoyang District, Beijing City 3, Institute of Microorganism, Academia Sinica

Detailed description of the invention

Fig. 1 .luminex liquid-phase chip detection schematic diagram；

Fig. 2 .GP73 single-factor standard items testing result；

Fig. 3 .AFU single-factor standard items testing result；

Fig. 4 .VEGF single-factor standard items testing result；

Fig. 5 .CD147 single-factor standard items testing result；

Fig. 6 .AFP single-factor standard items testing result；

Fig. 7 .CD147, VEGF double factor standard items testing result；

CD147 and VEGF double factor reacts in the same system, there is no cross reaction between antibody, each factor Reactivity worth does not have significant change.

Tri- factor standard product testing result of Fig. 8 .CD147, VEGF, AFP；

Tri- factor of CD147, VEGF and AFP is reacted in the same system, there is no cross reaction between antibody, it is each because The reactivity worth of son does not have significant change.

Tetra- factor standard product testing result of Fig. 9 .CD147, VEGF, AFP, AFU；

Tetra- factor of CD147, VEGF, AFP and AFU is reacted in the same system, there is no cross reaction between antibody, The reactivity worth of each factor does not have significant change.

Five factor standard product testing result of Figure 10 .CD147, VEGF, AFP, AFU, GP73；

Five factor of CD147, VEGF, AFP, AFU and GP73 is reacted in the same system, and there is no handing between antibody Fork reaction, the reactivity worth of each factor do not have significant change.

Wherein, abscissa is the concentration of standard items, and ordinate is fluorescence intensity.

Specific embodiment

Below by specific embodiment, the present invention is described in detail, it is to be understood that following embodiments are as solution It releases and illustrates, the range that the invention is not limited in any way.

Biomaterial

BALB/c mouse is purchased from Jie Sijie experimental animal Co., Ltd；

Hela cell is purchased from Guangzhou Sai Ku Bioisystech Co., Ltd；

Myeloma cell, Beijing blueness member Sheng Kang biological medicine Science and Technology Ltd. culture and preservation；

E.coli DH5 α competent cell, E.coliBL21 competent cell save for this laboratory, can be by commercially available It obtains.

Experiment reagent

Restriction enzyme EcoR I and Xho I is bought from Takara company, article No. D1040A, D1094A；

Carrier pET32a is bought from Novagen company, article No. VYN0176；

T4DNA ligase is bought from Takara company, article No. D2011A；

Plasmid extraction kit is bought from takara company, article No. 9760；

HyClone modified form RPMI-1640 culture medium is purchased from Hyclone company, article No. AB10113944；

Blood serum of newborn calf without mycoplasma (super) is purchased from Zhejiang Tian Hang Biotechnology Co., Ltd, article No. 22012-8612；

Dual anti-(100X) is purchased from Beijing Lei Gen Bioisystech Co., Ltd, article No. CA0075；

L-Glutamine (100X) is purchased from Amresco company, article No. Amresco 0374；

PEG (50%w/v polyethylene glycol 1,500) is purchased from Hampton company, article No. HR2-525；

HAT culture medium additive (50X) is purchased from gibco company, article No. 21060-017；

Sheep anti-mouse igg, purchased from green skies biology, article No. A0286；

Sodium acetate is purchased from Beijing chemical reagents corporation, article No. 10018892；

Octanoic acid is purchased from Beijing Jin Long chemical reagent Co., Ltd；

Streptavin-HRP (Streptavidin-horseradish peroxidase) is purchased from the green skies, article No. A0303；

Sulfo-NHS (N- hydroxy thiosuccinimide) is purchased from SIGMA company, article No. 56485；

EDC (1- (3- dimethylamino-propyl) -3- ethyl-carbodiimide hydrochloride) is purchased from SIGMA company, article No. 22980；

MES (2- (N- morpholine) ethanesulfonic acid) is purchased from SIGMA company, article No. M2933；

PBS-TBN (closing/store buffer liquid), PBS, containing 0.1%BSA (BSA is purchased from Kang Yuan biology), 0.02%TWEEN 20 (TWEEN 20 is purchased from Amresco 0777), 0.05%Azide (Azide is purchased from SIGMA S8032)；

Assay buffer (measurement buffer), PBS, containing 1%BSA (BSA is purchased from Kang Yuan biology) pH7.4；

Wash buffer (washing buffer), PBS, containing 0.02%TWEEN 20, (TWEEN 20 is purchased from Amresco 0777), pH7.4；

SAPE (streptavidin-phycoerythrin) is purchased from ebioscience company, article No. 12-4317；

Biotin is purchased from sigma company, article No. H1759；

Alpha-fetoprotein standard items are purchased from Nat'l Pharmaceutical & Biological Products Control Institute, product number 150542-1.

Instrument and consumptive material

Magnetic bead, be purchased from LUMINEX company, article No. MC10030-01, MC10034-01, MC10036-01, MC10038-01, MC10044-01；

Magnetic separator is purchased from Biorad company；

Luminex200 is purchased from BioRad company, model LUMINEX-200.

In following embodiments, not specified biological chemical reagent is this field conventional reagent, can be according to conventional side Method prepare and or it is commercially available, specification be the pure grade in laboratory；Not specified experiment equipment is this field routine Experiment equipment, it is commercially available.

It is prepared by the monoclonal antibody of 1. liver cancer related neoplasms marker of embodiment

(1) prepared by antigen

1. prepared by the antigen of Gorky's glycoprotein 73 (GP73)

Recombinant antigen design and preparation method are documented in: pangli monarch, the gene cloning and prokaryotic expression of Golgi apparatus protein, Medical forum's magazine, 2015 (9): 1-2.The antigen GP73-F3R3 of high-purity is prepared according to the method recorded in article, It expresses culture presevation in Beijing green member Sheng Kang biological medicine Science and Technology Ltd..

2. prepared by the antigen of alpha-L-fucosidase (AFU)

2.1 ANTIGEN DESIGNThe

466 amino acid of alpha-L-fucosidase overall length analyze α-L-fucose using DNA Star sequence analysis software The amino acid sequence (NCBI sequence number: NP_000138.2) of glycosides enzyme, obtains secondary structure, hydrophilic and hydrophobic, the antigenicity of albumen Etc. information.Comprehensively consider the antigenicity of protein sequence, specificity, Protein expression and purification it is ease, choose 252- The peptide fragment of 441aa is as antigen A FU-F2R2, and amino acid sequence is as shown in SEQ ID NO.1, gene coded sequence such as SEQ Shown in ID NO. 2.

2.2 antigen presentation

2.2.1 the acquisition of target fragment

(1) design of primers: EcoR I restriction enzyme site is introduced at 5 ' ends of forward primer, 5 ' ends of reverse primer introduce Xho I restriction enzyme site, obtained primer sequence are as follows:

AFU-F2:5 '-CGGAATTCGACAGCCCTGTCAAGGATGAG-3'；

AFU-R2:5 '-CCGCTCGAGGAAGAGACCTTTATCTGGATC-3’。

(2) acquisition of template DNA

Extract genomic DNA from Hela cell: method and steps is referring to " Molecular Cloning:A Laboratory guide ".

Reverse transcription obtains cDNA: method and steps is referring to " Molecular Cloning:A Laboratory guide ".

(3) target fragment is expanded according to following PCR system and program:

PCR system: 20ul

PCR program:

2.2.2 vector construction

(1) endonuclease reaction: restriction enzyme EcoR I and Xho I is used, respectively to target fragment and expression vector PET32a carries out double digestion.

Digestion system (100ul):

EcoRI:5ul

Xho I:5ul

10 × buffer: 10ul

Plasmid (8ng/ul): 55ul

H₂O:25ul

Digestion condition: 37 C overnights obtain linearisation PET-32a carrier and PCR digestion products.

(2) connection reaction:

Linked system (12ul):

Linearize PET-32a carrier (EcoR I/Xho I, 8ng/ul): 0.5ul

T4DNA ligase: 1ul

10 × buffer: 1.2ul

PCR digestion products (1ng/ul): 9.3ul

Condition of contact: room temperature connects 10h, obtains connection product.

2.2.3 protein expression and purifying

(1) Transformed E .coli DH5 α competent cell

After E.coli DH5 α competent cell places thawing on ice, connection product is added, stands 30min on ice.42 DEG C of heat 90s is handled, stands 2min on ice.It is added 600 μ L of LB culture medium, 37 DEG C, 150rpm shaking table culture 45min.Take 200 μ L bacterium solutions It is coated on amicillin resistance (Amp⁺) on LB plate, 37 DEG C are incubated overnight.

(2) positive clone identification

Picking single colonie, is inoculated in LB/Amp⁺Fluid nutrient medium in, 200rpm, 37 DEG C cultivate 8 hours, 8000rpm from Heart 5min collects thallus.Using plasmid extraction kit, to specifications in operating procedure extract plasmid.According to step 2.2.1 PCR system and program in carry out PCR verifying.PCR is identified that correct recombinant plasmid send raw work bioengineering limited Company's sequencing, the correct recombinant plasmid of comparison result is as expression vector.

(3) Transformed E .coli BL21 cell

After E.coli BL21 competent cell places thawing on ice, expression vector is added, stands 30min on ice.42 DEG C of heat 90s is handled, stands 2min on ice.It is added 600 μ L of LB culture medium, 37 DEG C, 150rpm shaking table culture 45min.Take 200 μ L bacterium solutions It is coated on Amp⁺On resistance LB plate, 37 DEG C are incubated overnight.

(4) protein expression

Picking single colonie is inoculated in the Amp of 5ml⁺In resistance LB liquid medium, 37 DEG C of overnight incubations take and are incubated overnight The fresh Amp of 3ml is added in object 140ul⁺In resistance LB liquid medium, 37 DEG C of cultures reach OD₆₀₀It is 0.5 or so, is added 1/ 1000IPTG (0.8M), 37 DEG C, 180rmp cultivates 4h.Run 10% SDS-PAGE judgement induction situation.

(5) protein purification

Using ammonium sulfate precipitation method purifying protein: sample being centrifuged, removal precipitating retains supernatant and measures volume；One The addition ammonium sulfate of side stirring on one side slowly.Then, solution is placed on magnetic stirring apparatus and is stirred

6h or 4 DEG C is stirred overnight, and precipitates protein sufficiently.By protein solution centrifugation, it is heavy to abandon supernatant reservation It forms sediment.The PBS- sodium azide solution solubilising protein of 10-20ml is added.After albumen precipitation dissolution, it is put into bag filter and dialyses 24-48h removes ammonium sulfate every 5h replacement dialyzate.Dialyzate is collected, centrifugation measures the content of protein in supernatant.

3. prepared by the antigen of vascular endothelial growth factor (VEGF)

3.1 ANTIGEN DESIGNThe

Use amino acid sequence (the NCBI sequence of DNA Star sequence analysis software analysis human vascular endothelial growth factor Number: NP_001020539.2), according to the information such as the secondary structure of albumen, hydrophilic and hydrophobic, antigenicity and the difference of each variant Effect, selects the peptide fragment of 165 amino acid of 207-371aa as antigen VEGF-FR, amino acid sequence such as SEQ ID Shown in NO.5, gene coded sequence is as shown in SEQ ID NO.6.

3.2 antigen presentation

3.2.1 the acquisition of target fragment

VEGF-F:5 '-CGGAATTCGCACCCATGGCAGAAGGAGGAG-3'；

VEGF-R:5 '-CCGCTCGAGCCGCCTCGGCTTGTCACATCTG-3’。

(2) cDNA obtained using 2.2.1 expands target fragment according to following PCR system and program as template:

PCR system: 20ul

PCR program:

3.2.2 vector construction

The same 2.2.2 of construction method.

3.2.3 protein expression and purifying

Host strain and the same 2.2.3 of expression and purification method.

4. prepared by the antigen of extracellular matrix metalloproteinase (CD147)

4.1 ANTIGEN DESIGNThe

Using DNA Star sequence analysis software analysis people CD147 amino acid sequence (protein ID: BAC76828.1), comprehensively consider the antigenicity of protein sequence, specificity, Protein expression and purification it is ease, choose 25- The peptide fragment of 177aa is as Antigens CD14 7-F3R3, and amino acid sequence is as shown in SEQ ID NO.9, and gene coded sequence is such as Shown in SEQ ID NO.10.

4.2 antigen presentation

4.2.1 the acquisition of target fragment

CD147-F3:5’-CGGAATTCACAGTCTTCACTACCGTAGAAG-3'；

CD147-R3:5’-CGCTCGAGCTCCATGTTCAGGTTCTCAATG-3’。

PCR system: 20ul

PCR program:

4.2.2 vector construction

The same 2.2.2 of construction method.

4.2.3 protein expression and purifying

Host strain and the same 2.2.3 of expression and purification method.

(2) Antibody preparation

1. immune mouse

Prepare 8-12 weeks BALB/c mouse two (two mouse are immunized in every kind of antigen) after being born, is pressed with the antigen of high-purity Two mouse are immunized according to following method:

First immunisation takes the emulsification of 100ug antigen+100ul Freund's complete adjuvant to mix injection mouse vola, and about 80ul/ is only；Second It is secondary immune, take the emulsification of 100ul antigen+100ul Freund's incomplete adjuvant to mix injection mouse vola, about 80ul/ is only；Third and fourth, five It is secondary immune, it is immune with second.

2. cell fusion

All operations are completed in super-clean bench below.

(1) take out myeloma cell from incubator, poured into centrifuge tube after blowing attached cell open, be centrifuged 5min, 2000 Turn, supernatant is abandoned after centrifugation, the RPMI-1640 culture medium (dual anti-containing 2/1) that 40ml ice-water bath is added mixes for use.

(2) prepare three culture dishes, pour into the RPMI-1640 culture medium (dual anti-containing 2/1) of ice-water bath respectively, take mouse big Inboard leg lymphocyte, is put into first culture dish by two, starts to cut off the adipose tissue and knot torn on lymphocyte Tissue is formed, is moved into second culture dish, lymph node cells is cleaned, then move into third culture dish, starts to tear up lymph node Allow cell to release, and blown and beaten back and forth with dropper it is several under, stronger releases cell, then starts filtration cell and (uses band There is the suction pipe of cotton to be filled into centrifuge tube) it is centrifuged together to 40ml, and labeled as lymph node cells and myeloma cell, 10min, respectively abandons supernatant 30ml, starts counting by 2000 turns/min after centrifugation, in proportion by lymph node cells and myeloma cell (GP73 1:3, AFU 2:3, VEGF 2:3, CD147 1:1) is mixed, and the RPMI-1640 culture medium of ice-water bath is added extremely 50ml, is centrifuged 5min, 2000 turns/min, abandons supernatant and adds the RPMI-1640 culture medium of ice-water bath to 50ml, be centrifuged 5min, 2000 turns/min, supernatant is abandoned, the RPMI-1640 culture medium of heat is added to 50ml, is centrifuged 5min, 2000 turns/min.

(3) it is initially added into PEG: taking out the lymph node cells after mixing and being centrifuged and myeloma cell, abandon supernatant, blot net Remaining RPMI-1640 culture medium in centrifuge tube takes out about 0.8ml PEG and is drop by drop added in centrifuge tube, and along with light Micro- friction, rocks, and after addition, is put into 37 degree of water baths and is incubated for one minute, and PEG is made to be easier to bond.

(4) cell after water-bath is taken out, the RPMI-1640 culture medium of heat is slowly added in beginning, one after another drop of that simultaneously companion is added With rocking, until 35ml, then 50ml is added to, is centrifuged 10min, 1000 turns/min.

(5) 200ml culture solution (culture medium additive containing HAT (50X), dual anti-(100X), L-Glutamine (100X) are prepared And 20% blood serum of newborn calf without mycoplasma), feeder cells containing 10ml.

(6) supernatant is removed after cell centrifugation, 200ml culture solution is added, mixes, the hole bed board 185ul/, 10 blocks of plates, label 1 arrives It No. 10, is put into incubator.Plate is merged in viewing in the 6th day after fusion, and marks cell hole and monoclonal hole, to look into after detecting It looks for.

3. the screening and detection of hybridoma

(1) it is coated with fast testing plate: using antigen coat, 2ug/ml, the hole 50ul/, totally two ten blocks of plates.With 1xPBS dilution It is added in detection plate after mixing antigen, 37 degree are incubated for 2 hours, wash five times, confining liquid are added after patting dry, the hole 180ul/, 37 degree incubate Educate 1 hour, pat dry, be put into 4 degree it is stand-by.

(2) ten pieces of fast testing plates are taken out and take out 1 to No. 10 fusion plates, the corresponding one block of fusion plate of one piece of detection plate carries out ELISA detection, from fusion plate in take cells and supernatant be added detection plate in, the hole 50ul/, leave and take last four hole respectively as Two negative holes and positive hole, 37 degree are incubated for 1 hour, take out detection plate, abandon supernatant, board-washing five times, pat dry, and are added 1:10000 times Diluted sheep anti mouse secondary antibody (dilution PBST-BSA), the hole 50ul/, 37 degree 1 hour, board-washing 5 times, pat dry, be added TMB colour developing Ten minutes, terminate liquid is added, reading marks positive cell hole.

1 to No. 10 fusion plates are carried out ELISA detection by the ten pieces of new fast testing plates of taking-up in (2) second days again, are read Number marks positive cell hole.The cell hole for detecting all be positive cell hole and readings 1 or more twice is selected, GP73 is 17 plants, AFU is 12 plants, and VEGF is 10 plants, and CD147 is 10 plants, prepares clone.

(3) detection of monoclonal antibody: with 400ml culture solution (culture medium additive containing HAT (50X), dual anti-(100X), L-Glutamine (100X), 20% blood serum of newborn calf without mycoplasma), feeder cells containing 20ml.The every hole of microscopically observation is thin Born of the same parents' quantity takes out about 80 cell quantity, average bed board, and the hole 190ul/ is put into incubator, cultivates seven days, viewing clone Plate records monoclonal hole, and carries out ELISA detection, according to OD₄₅₀> 0.8 screening criteria selects monoclonal antibody strain.

(4) after selecting monoclonal antibody strain, new culture solution (containing feeder cells) is added, is put into incubator and cultivates. After four days, clone's plate viewing cell quantity and culture solution color are opened, cell concentration, which covers with, accounts for about hole 2/3, watches cell hole In cell state.

GP73 singling: 2F10A4,4D3D5,7B7B3,1C10B5,1G9C8,3D10B5,4G8D7,8F10D1, 10B9F11,10C11B1,4G8E12 and 7E11D11.

AFU singling: 1E1D1,3B6C3,3F12D8,1A4H4,3F12E4,10E11G10,10F10G10,5F2C3, 7B9H5,4G1H4,5E5A5,5E5G5,5F2D7.

VEGF singling: 1D2E5,3B1D8,4C3D12,4D3E5,5C7F10,5E1C3,7A11D4,7A11E10, 8E10D8。

CD147 singling: 1A2D8,3D6C6,4A4C3,5A4E9,5C9G1,6A1D4,6B7F12.

(5) it is coated with one piece of fast testing plate, detects the cell in 24 holes.

4. preparing ascites

(1) prepare 20 mouse given birth to, inject paraffin oil, about 1ml/ is only.

(2) cell covered in 24 holes is passed to six holes, is passed in bottle after being covered in six holes, covers in the vial again Afterwards, cell is injected in mouse abdomen.

(3) mouse web portion is watched after 15 days, ascites can be extracted by big tripe situation occur, handle ascites, centrifugation 10min 2000 turns/min, leaves and takes supernatant, it is spare to be stored in minus 20 degrees.

5. ascites antibody purification

Using sorvall 50ml centrifuge tube as reaction vessel, using sad method, Purified monoclonal is anti-from mouse ascites Body, experimental procedure are as follows:

(1) 10ml ascites is centrifuged 30min in room temperature 20000rpm；

(2) it takes 10ml supernatant that 4.0 sodium-acetate buffer of 20ml 0.06M PH is added, then adjusts PH with 1M NaOH To PH 4.8；

(3) 750ul octanoic acid is added dropwise, room temperature quickly stirs 30min；Then room temperature centrifugal mixture 20000rpm, 30min；Supernatant carefully is poured out, and siphons away the supernatant that sediment adheres to above with pipette tips；

(4) twice with 1L 0.1M PH 6.5NaPO4,4mM EDTA dialysis, it changes a not good liquor within 3 hours, obtains antibody-solutions, Measure protein concentration.

Embodiment 2. is used for the antibody of double-antibody method detection to pairing

(1) ELISA double antibodies sandwich pairing experiment

In accordance with the following steps, it is real that the monoclonal antibody for purifying each obtained albumen to embodiment 1 respectively carries out pairing It tests:

1, be coated with: coated antibody (embodiment 1 purifies obtained one of monoclonal antibody) is diluted to 5ug/ml with PBS (PH=7.4). Every hole 100ul, 37 DEG C of coating 1h.

2, board-washing: PBST is washed 5 times, is patted dry.

3, close: confining liquid (contains 3%BSA and 4% sucrose PBS), every hole 200ul, 37 DEG C of closing 1h.

4, dry: not board-washing pats dry raffinate, air-dries 30min.

5, antigen is added: antigen (antigen purified in embodiment 1) is diluted with the PBS (PH=7.4) containing 1%BSA To 2ug/ml, ELISA Plate is added, from the 1st hole (2ug/ml) doubling dilution to the 11st hole (0.2ng/ml), every hole 100ul, the 12nd The PBS (PH=7.4) of Kong Jiahan 1%BSA is used as negative control, 37 DEG C of incubation 40min.

6, board-washing: PBST is washed 5 times, is patted dry.

7, detection antibody is added: with the monoclonal antibody (embodiment 1 of PBS (PH=7.4) the dilution biotin labeling containing 1%BSA Purify obtained one of monoclonal antibody), ELISA Plate, every hole 100ul, 37 DEG C of incubation 40min are then added.

8, board-washing: PBST is washed 5 times, is patted dry.

9, Streptavin-HRP is added: diluting Streptavin-HRP, every hole with the PBS (PH=7.4) containing 1%BSA 100ul, 37 DEG C of effect 30min.

10, board-washing: PBST is washed 5 times, is patted dry.

11, develop the color: tetramethyl benzidine (TMB) 100ul colour developing is added in every hole.

12, terminate reaction: 1M H is added in every hole₂SO₄100ul, microplate reader readings.

As a result as shown in the table:

Table 1.GP73 double antibodies sandwich matches experimental result

Table 2.AFU double antibodies sandwich matches experimental result

Table 3.VEGF double antibodies sandwich matches experimental result

Table 4.CD147 double antibodies sandwich matches experimental result

Using alpha-fetoprotein standard items as antigen, it is existing that this laboratory is detected according to above-mentioned ELISA double antibodies sandwich experimental procedure Anti- AFP antibody to (coated antibody 3B11H5 and detection antibody 2G5E8), the results showed that, the antigen inspection of AntiAFP antibody pair The survey limit is 1.6ng/ml.

(2) pairing antibody verifies the detection effect of serum

Experimental procedure is matched according to above-mentioned ELISA double antibodies sandwich, using human serum as antigen, preferable antibody pair is matched in verifying Detection effect, filter out the best antibody of detection effect and China General Microbiological culture presevation administrative center sent to be protected Hiding is as a result as follows:

GP73: coated antibody 8F10D1, detect antibody 10B9F11；

AFU: coated antibody 3F12D8 (CGMCC NO:13583) is detected antibody 10F10G10 (CGMCC NO:13584)；

VEGF: coated antibody 7A11D4 (CGMCC NO:13585) is detected antibody 8E10D8 (CGMCC NO:13586)；

CD147: coated antibody 4A4C3 (CGMCC NO:13587) is detected antibody 6B7F12 (CGMCC NO:13588)；

AFP: coated antibody 3B11H5 (CGMCC NO:13581) is detected antibody 2G5E8 (CGMCC NO:13582).

The coupling of 3. antibody of embodiment and label

1, the coupling of magnetic bead and coated antibody

(1) clean magnetic bead: suspend be not coupled magnetic bead (MC10030-01, MC10034-01, MC10036-01, MC10038-01, MC10044-01), transfer 5.0 × 10⁶Centrifuge tube is put on magnetic separator by a magnetic bead into centrifuge tube 30-60s is separated, supernatant is sucked out, 100ul dH is added₂O vortex suspends magnetic bead again, and 30-60s is separated on magnetic separator, inhales Supernatant out.

(2) 80ul 0.1M NaH activated magnetic beads: is added₂PO₄(Ph6.2), vortex suspension magnetic bead；Add 10ul 50mg/ Ml sulfo-NHS (N- hydroxy thiosuccinimide) and 10ul 50mg/ml EDC (1- (3- dimethylamino-propyl) -3- second Base carbodiimide hydrochloride), it is vortexed and mixes, be incubated at room temperature 20 minutes to activate microballoon.Then 250ul 50mM is used Ph5.0MES (2- (N- morpholine) ethanesulfonic acid) solution is washed twice, to remove unassembled sulfo-NHS and EDC.

(3) antibody-coupled magnetic beads: magnetic bead is resuspended in the magnetic bead after taking 100ul 50mM MES (Ph5.0) that activation is added, takes 10-20ug embodiment 2 screens obtained best coated antibody and (a kind of albumen correspond to a kind of magnetic bead) is added in corresponding magnetic bead, It is settled to 500ul with MES, is protected from light at room temperature 2 hours.Centrifuge tube is put on magnetic separator and separates 30-60s, is sucked out Supernatant.

(4) it saves the magnetic bead of coupled antibody: 500ul PBS-TBN is added as Block buffer, at room temperature whirling vibration It is incubated for 30 minutes.Centrifuge tube is put on magnetic separator and separates 30-60s, removes supernatant, uses 1ml PBS-TBN as cleaning Buffer is washed twice, and supernatant is sucked out, and 4 DEG C of 250-1000ul PBS-TBN preservations are added.

(5) confirmation of antibody coupling efficiency: the magnetic bead (microballoon group) after diluting antibody coupling with assay buffer makes it 96 orifice plates, the hole 50ul/ is added in final concentration of 50 magnetic beads/ul.The sheep anti-mouse igg of biotin labeling is diluted to 4ug/ml, 50ul, blank pair is added in 2ug/ml, 1ug/ml, 0.5ug/ml, 0.25ug/ml, 0.125ug/ml, 0.0625ug/ml, every hole According to 50ul assay buffer is added, room temperature concussion is incubated for 30min, and wash buffer is washed 3 times, and the hole SAPE 50ul/ is added, Shaken at room temperature is incubated for 30 minutes, and wash buffer is washed 2 times, is eventually adding machine on 80ul assay buffer (luminex200) it detects, as a result as shown in the table.

6 tumor markers antibody coupling of table confirms result

2, the biotin labeling of antibody is detected

2mg biotin (sigma) is dissolved in 200ul solvent DMSO, the best inspection that will be screened in embodiment 2 It surveys antibody and is dissolved to 1mg/ml 450ul with the carbonic acid buffer of PH=9.6.The life dissolved is added into detection antibody-solutions Object element 50ul (organic solvent accounts for system 10%, and biotin is excessive), adds 500ul pure glycerin after reacting at room temperature 4h, is stored in -20 It is spare in DEG C refrigerator.

4. standard curve making of embodiment

The antigen that embodiment 1 is prepared carries out 4 times of gradient dilutions with assay buffer, obtains concentration and is respectively 1000ng/ml, 250ng/ml, 64ng/ml, 16ng/ml, 4ng/ml, 1ng/ml, 0.25ng/ml antigenic solution, while with Assay buffer is as blank control.

After the magnetic bead being coupled in embodiment 3 is diluted well with assay buffer, it is protected from light every hole in 96 orifice plates and is added 50ul, 96 orifice plates are put on magnetic sheet, and 120ul wash buffer is added in every hole, are stood 2 minutes, are outwelled wash buffer, add Enter the antigen of various concentration gradient, 4 DEG C of reaction overnights (15-18h), wash buffer is washed three times；The biology diluted is added The detection antibody of element label, the hole 50ul/, 800 revs/min of room temperature are incubated for 30 minutes；Wash buffer is washed three times；SAPE is added, The hole 50ul/, 800 revs/min of room temperature are incubated for 30 minutes, and wash buffer is washed twice, and machine examination on 80ul assay buffer is added It surveys, as a result as shown in Fig. 2-6, AFP, GP73, AFU, VEGF susceptibility can reach 250pg/ml, and CD147 susceptibility can reach 64pg/ml。

CD147/VEGF double factor, tri- factor of CD147/VEGF/AFP, CD147/VEGF/ AFP/AFU are additionally carried out Four factors and five factor standard product examine of CD147/VEGF/AFP/AFU/GP73 are surveyed.Specific detection method is same as above, difference It is: (1) magnetic bead for being coupled different tumor markers coated antibodies is mixed into a system；(2) antigen is different tumours The mixed liquor of marker antigen；(3) detection antibody is the different tumor-marker analyte detection antibody of the biotin labeling diluted Mixed liquor.

As a result as shown in table 7-10:

Table 7.CD147, VEGF double factor standard items testing result

Tri- factor standard product testing result of table 8.CD147, VEGF, AFP

Tetra- factor standard product testing result of table 9.CD147, VEGF, AFP, AFU

Five factor standard product testing result of table 10.CD147, VEGF, AFP, AFU, GP73

Multiple-factor testing result shows that coated antibody provided by the present invention and detection antibody have the advantage that

(1) high specificity: reactivity worth and list when multipair antibody detects multiple protein simultaneously in same reaction system Between each factor antibody and other factors cross reaction does not occur for reactivity worth when solely detecting every kind of albumen without significant change.

(2) accuracy is good: in same reaction system, cross reaction does not occur between each factor antibody.

(3) high sensitivity: in same reaction system, AFP is detected, the sensitivity of GP73, AFU, VEGF can reach 250pg/ml, the sensitivity for detecting CD147 can reach 64pg/ml.

SEQUENCE LISTING

<110>horse, it is outstanding

<120>for detecting the antibody and kit of CD147 in serum

<130>P160547/YAY

<160> 12

<170> PatentIn version 3.5

<210> 1

<211> 190

<212> PRT

<213> Artificial Sequence

<220>

<223>amino acid sequence of alpha-L-fucosidase antigen

<400> 1

Asp Ser Pro Val Lys Asp Glu Val Val Val Asn Asp Arg Trp Gly Gln

1 5 10 15

Asn Cys Ser Cys His His Gly Gly Tyr Tyr Asn Cys Glu Asp Lys Phe

20 25 30

Lys Pro Gln Ser Leu Pro Asp His Lys Trp Glu Met Cys Thr Ser Ile

35 40 45

Asp Lys Phe Ser Trp Gly Tyr Arg Arg Asp Met Ala Leu Ser Asp Val

50 55 60

Thr Glu Glu Ser Glu Ile Ile Ser Glu Leu Val Gln Thr Val Ser Leu

65 70 75 80

Gly Gly Asn Tyr Leu Leu Asn Ile Gly Pro Thr Lys Asp Gly Leu Ile

85 90 95

Val Pro Ile Phe Gln Glu Arg Leu Leu Ala Val Gly Lys Trp Leu Ser

100 105 110

Ile Asn Gly Glu Ala Ile Tyr Ala Ser Lys Pro Trp Arg Val Gln Trp

115 120 125

Glu Lys Asn Thr Thr Ser Val Trp Tyr Thr Ser Lys Gly Ser Ala Val

130 135 140

Tyr Ala Ile Phe Leu His Trp Pro Glu Asn Gly Val Leu Asn Leu Glu

145 150 155 160

Ser Pro Ile Thr Thr Ser Thr Thr Lys Ile Thr Met Leu Gly Ile Gln

165 170 175

Gly Asp Leu Lys Trp Ser Thr Asp Pro Asp Lys Gly Leu Phe

180 185 190

<210> 2

<211> 570

<212> DNA

<213> Artificial Sequence

<220>

<223>gene coded sequence of alpha-L-fucosidase antigen

<400> 2

gacagccctg tcaaggatga ggtggtagta aatgaccgat ggggtcagaa ctgttcctgt 60

caccatggag gatactataa ctgtgaagat aaattcaagc cacagagctt gccagatcac 120

aagtgggaga tgtgcaccag cattgacaag ttttcctggg gctatcgtcg tgacatggca 180

ttgtctgatg ttacagaaga atctgaaatc atttcggaac tggttcagac agtaagtttg 240

ggaggcaact atcttctgaa cattggacca actaaagatg gactgattgt tcccatcttc 300

caagaaaggc ttcttgctgt tgggaaatgg ctgagcatca atggggaggc tatctatgcc 360

tccaaaccat ggcgggtgca atgggaaaag aacacaacat ctgtatggta tacctcaaag 420

ggatcggctg tttatgccat ttttctgcac tggccagaaa atggagtctt aaaccttgaa 480

tcccccataa ctacctcaac tacaaagata acaatgctgg gaattcaagg agatctgaag 540

tggtccacag atccagataa aggtctcttc 570

<210> 3

<211> 29

<212> DNA

<213> Artificial Sequence

<220>

<223>the PCR forward primer AFU-F2 of alpha-L-fucosidase antigen encoding sequences

<400> 3

cggaattcga cagccctgtc aaggatgag 29

<210> 4

<211> 30

<212> DNA

<213> Artificial Sequence

<220>

<223>the PCR reverse primer AFU-R2 of alpha-L-fucosidase antigen encoding sequences

<400> 4

ccgctcgagg aagagacctt tatctggatc 30

<210> 5

<211> 165

<212> PRT

<213> Artificial Sequence

<220>

<223>amino acid sequence of vascular endothelial growth factor antigen

<400> 5

Ala Pro Met Ala Glu Gly Gly Gly Gln Asn His His Glu Val Val Lys

1 5 10 15

Phe Met Asp Val Tyr Gln Arg Ser Tyr Cys His Pro Ile Glu Thr Leu

20 25 30

Val Asp Ile Phe Gln Glu Tyr Pro Asp Glu Ile Glu Tyr Ile Phe Lys

35 40 45

Pro Ser Cys Val Pro Leu Met Arg Cys Gly Gly Cys Cys Asn Asp Glu

50 55 60

Gly Leu Glu Cys Val Pro Thr Glu Glu Ser Asn Ile Thr Met Gln Ile

65 70 75 80

Met Arg Ile Lys Pro His Gln Gly Gln His Ile Gly Glu Met Ser Phe

85 90 95

Leu Gln His Asn Lys Cys Glu Cys Arg Pro Lys Lys Asp Arg Ala Arg

100 105 110

Gln Glu Asn Pro Cys Gly Pro Cys Ser Glu Arg Arg Lys His Leu Phe

115 120 125

Val Gln Asp Pro Gln Thr Cys Lys Cys Ser Cys Lys Asn Thr Asp Ser

130 135 140

Arg Cys Lys Ala Arg Gln Leu Glu Leu Asn Glu Arg Thr Cys Arg Cys

145 150 155 160

Asp Lys Pro Arg Arg

165

<210> 6

<211> 495

<212> DNA

<213> Artificial Sequence

<220>

<223>gene coded sequence of vascular endothelial growth factor antigen

<400> 6

gcacccatgg cagaaggagg agggcagaat catcacgaag tggtgaagtt catggatgtc 60

tatcagcgca gctactgcca tccaatcgag accctggtgg acatcttcca ggagtaccct 120

gatgagatcg agtacatctt caagccatcc tgtgtgcccc tgatgcgatg cgggggctgc 180

tgcaatgacg agggcctgga gtgtgtgccc actgaggagt ccaacatcac catgcagatt 240

atgcggatca aacctcacca aggccagcac ataggagaga tgagcttcct acagcacaac 300

aaatgtgaat gcagaccaaa gaaagataga gcaagacaag aaaatccctg tgggccttgc 360

tcagagcgga gaaagcattt gtttgtacaa gatccgcaga cgtgtaaatg ttcctgcaaa 420

aacacagact cgcgttgcaa ggcgaggcag cttgagttaa acgaacgtac ttgcagatgt 480

gacaagccga ggcgg 495

<210> 7

<211> 30

<212> DNA

<213> Artificial Sequence

<220>

<223>the PCR forward primer VEGF-F of vascular endothelial growth factor antigen encoding sequences

<400> 7

cggaattcgc acccatggca gaaggaggag 30

<210> 8

<211> 31

<212> DNA

<213> Artificial Sequence

<220>

<223>the PCR reverse primer VEGF-R of vascular endothelial growth factor antigen encoding sequences

<400> 8

ccgctcgagc cgcctcggct tgtcacatct g 31

<210> 9

<211> 153

<212> PRT

<213> Artificial Sequence

<220>

<223>amino acid sequence of CD147 antigen

<400> 9

Thr Val Phe Thr Thr Val Glu Asp Leu Gly Ser Lys Ile Leu Leu Thr

1 5 10 15

Cys Ser Leu Asn Asp Ser Ala Thr Glu Val Thr Gly His Arg Trp Leu

20 25 30

Lys Gly Gly Val Val Leu Lys Glu Asp Ala Leu Pro Gly Gln Lys Thr

35 40 45

Glu Phe Lys Val Asp Ser Asp Asp Gln Trp Gly Glu Tyr Ser Cys Val

50 55 60

Phe Leu Pro Glu Pro Met Gly Thr Ala Asn Ile Gln Leu His Gly Pro

65 70 75 80

Pro Arg Val Lys Ala Val Lys Ser Ser Glu His Ile Asn Glu Gly Glu

85 90 95

Thr Ala Met Leu Val Cys Lys Ser Glu Ser Val Pro Pro Val Thr Asp

100 105 110

Trp Ala Trp Tyr Lys Ile Thr Asp Ser Glu Asp Lys Ala Leu Met Asn

115 120 125

Gly Ser Glu Ser Arg Phe Phe Val Ser Ser Ser Gln Gly Arg Ser Glu

130 135 140

Leu His Ile Glu Asn Leu Asn Met Glu

145 150

<210> 10

<211> 459

<212> DNA

<213> Artificial Sequence

<220>

<223>gene coded sequence of antigen

<400> 10

acagtcttca ctaccgtaga agaccttggc tccaagatac tcctcacctg ctccttgaat 60

gacagcgcca cagaggtcac agggcaccgc tggctgaagg ggggcgtggt gctgaaggag 120

gacgcgctgc ccggccagaa aacggagttc aaggtggact ccgacgacca gtggggagag 180

tactcctgcg tcttcctccc cgagcccatg ggcacggcca acatccagct ccacgggcct 240

cccagagtga aggctgtgaa gtcgtcagaa cacatcaacg agggggagac ggccatgctg 300

gtctgcaagt cagagtccgt gccacctgtc actgactggg cctggtacaa gatcactgac 360

tctgaggaca aggccctcat gaacggctcc gagagcaggt tcttcgtgag ttcctcgcag 420

ggccggtcag agctacacat tgagaacctg aacatggag 459

<210> 11

<211> 30

<212> DNA

<213> Artificial Sequence

<220>

<223>the PCR forward primer CD147-F3 of CD147 antigen encoding sequences

<400> 11

cggaattcac agtcttcact accgtagaag 30

<210> 12

<211> 30

<212> DNA

<213> Artificial Sequence

<220>

<223>the PCR reverse primer CD147-R3 of CD147 antigen encoding sequences

<400> 12

cgctcgagct ccatgttcag gttctcaatg 30

Claims

1. the antibody pair for detecting liver cancer marker CD147 in test serum, which is characterized in that resisted by first antibody and second Body composition；The first antibody is secreted as coated antibody by the hybridoma that deposit number is CGMCC NO:13587；Institute Secondary antibody is stated as detection antibody, is secreted by the hybridoma that deposit number is CGMCC NO:13588.

2. being used for the kit of hepatocarcinoma early diagnosis, which is characterized in that including antibody pair described in claim 1, and be used for The common reagent of immune detection.

3. kit according to claim 2, which is characterized in that the first antibody and magnetic bead are coupled, and described second is anti- Body biotin labeling, the common reagent for immune detection are streptavidin-phycoerythrin.

4. kit according to claim 2, which is characterized in that further include the standard items of CD147 and/or with described The standard curve or linear regression equation specification of the standard items production of CD147.

5. according to any kit of claim 2-4, which is characterized in that further include antibody, the anti-height of anti-alpha-fetoprotein Antibody, the antibody of anti-alpha-L-fucosidase and/or the antibody of anti-vascular endothelial growth factor and its phase of your base glycoprotein 73 The immunologic function test reagent answered.

6. kit according to claim 5, which is characterized in that further include alpha-fetoprotein, Gorky's glycoprotein 73, α-L- The standard items of fucosidase and/or vascular endothelial growth factor, and/or with alpha-fetoprotein, Gorky's glycoprotein 73, α-L- rock Algae glycosidase and/or the standard curve or linear regression equation specification of the production of the standard items of vascular endothelial growth factor.