[go: up one dir, main page]

Ingham et al., 1981 - Google Patents

Fluorescent labeling of the carbohydrate moieties of human chorionic gonadotropin and α1-acid glycoprotein

Ingham et al., 1981

Document ID
864113038203613531
Author
Ingham K
Brew S
Publication year
Publication venue
Biochimica et Biophysica Acta (BBA)-Protein Structure

External Links

Snippet

A method for covalent attachment of a fluorescent molecule to the carbohydrate moieties of glycoproteins is described. The glycoproteins were oxidized with periodate under mild conditions selective for sialic acid (Van Lenten, L. and Ashwell, G.(1971) J. Biol. Chem. 246 …
Continue reading at www.sciencedirect.com (other versions)

Classifications

    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
    • G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53—Immunoassay; Biospecific binding assay
    • G01N33/531—Production of immunochemical test materials
    • G01N33/532—Production of labelled immunochemicals
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
    • G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/06—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents
    • C07K1/061—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents using protecting groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans

Similar Documents

Publication Publication Date Title
Ingham et al. Fluorescent labeling of the carbohydrate moieties of human chorionic gonadotropin and α1-acid glycoprotein
CA1303496C (en) Ck-mm myocardial infarction immunoassay
Chicheportiche et al. Synthesis of new, highly radioactive tetrodotoxin derivatives and their binding properties to the sodium channel
Fields et al. Micro method for determination of reactive carbonyl groups in proteins and peptides, using 2, 4-dinitrophenylhydrazine
EP0028332B1 (en) Beta-galactosyl-umbelliferone-labeled protein and polypeptide conjugates, and n-substituted 7-beta-galactosylcumarin-3-carboxamides
EP0224120A2 (en) Protein label and drug delivery system
CA2105181C (en) Compounds and methods for sequencing amino acids
Foster et al. Conformation-dependent limited proteolysis of bovine plasma albumin by an enzyme present in commercial albumin preparations
US20080227092A1 (en) Solid-Phase Oligosaccharide Tagging: a Technique for Manipulation of Immobilized Carbohydrates
Sator et al. Pyrenesulfonyl azide: a marker of acetylcholine receptor subunits in contact with membrane hydrophobic environment
Burstein et al. Selective chemical cleavage of tryptophanyl peptide bonds in peptides and proteins
Grammer et al. Chemistry and mechanism of vanadate-promoted photooxidative cleavage of myosin
Merz Studies of the Specific Role of the Subunits of Choriogonadotropin for Biological, Immunological and Physical Properties of the Hormone: Digestion of the α‐Subunit with Carboxypeptidase A
US6828417B2 (en) Polypeptide and process for measuring living body components using the same
Fontana et al. [40] Sulfenyl halides as modifying reagents for polypeptides and proteins
Cheung et al. Fluorescence energy transfer studies on the proximity of the two essential thiols of myosin subfragment-1.
Bock [27] Thioester peptide chloromethyl ketones: Reagents for active site-selective labeling of serine proteinases with spectroscopic probes
Matuszczyk et al. Development of an ELISA for 2, 4-D: characterization of two polyclonal antisera
Chen et al. Micellar capillary electrophoresis separation and thermo‐optical absorbance detection of products from manual peptide sequencing
Flanders et al. Semisynthetic derivatives of glucagon:(Des-His1) N. epsilon.-acetimidoglucagon and N. alpha.-biotinyl-N. epsilon.-acetimidoglucagon
Timkovich Chemical modification of the haem propionate of cytochrome c
Levy et al. The trifluoroacetylation of insulin
Sigrist et al. Group-directed modification of bacteriorhodopsin by arylisothiocyanates: Labeling, identification of the binding site and topology
Kanaya et al. Determination of low concentrations of protein by the biuret method using the “stopped-flow time difference analysis” technique
Burstein et al. Use of a nonenzymic cleavage reaction for the identification of exposed tyrosine residues in bovine pancreatic ribonuclease