Chromogranin A detection reagent, detection reference interval and detection method

A chromaffin protein and detection reagent technology, applied in chromaffin A detection reagent and detection reference interval and detection field, can solve the complicated operation steps of enzyme-linked immunoassay, poor sensitivity of immunoradiometric assay, and sensitivity of fluorescence immunoassay. It can reduce the probability of false negatives and false positives, improve the detection accuracy, and shorten the detection cycle.

Inactive Publication Date: 2019-03-22
EPITOPE BIOTECH
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  • Abstract
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  • Claims
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Problems solved by technology

[0009] However, due to the inherent characteristics of the methodology, the above listed products all have certain defects.
For example, the enzyme-linked immunoassay method has cumbersome operation steps and takes a long time to react; t

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  • Chromogranin A detection reagent, detection reference interval and detection method
  • Chromogranin A detection reagent, detection reference interval and detection method
  • Chromogranin A detection reagent, detection reference interval and detection method

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Embodiment Construction

[0066] The present invention will be specifically introduced below in conjunction with the accompanying drawings and specific embodiments.

[0067] A detection reagent for chromogranin A, comprising: an immune complex and an antibody detection system;

[0068] The immune complex is composed of labeled first specific antibody, labeled second specific antibody, chromogranin A calibrator, chromogranin A quality control substance, and the sample to be tested;

[0069] The first specific antibody and the second specific antibody are formed by specific binding of the antibody to the amino acid site in the amino acid sequence of human chromogranin A.

[0070] Wherein at least one antibody specifically binds to the epitope of amino acids 1-113 in the amino acid sequence of human chromogranin A, and wherein at least 3 consecutive amino acids are located in fragment 38-63;

[0071] wherein at least one antibody specifically binds to the epitope of amino acids 131-143 in the amino acid ...

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Abstract

The invention discloses a chromogranin A detection reagent. The chromogranin A detection reagent comprises an immune complex and an antibody detection system, wherein the immune complex is formed by compounding a marked first specific antibody, a marked second specific antibody, a chromogranin A calibration product, a chromogranin A quality control product and a sample to be detected; the first specific antibody and the second specific antibody are formed by carrying out epitope specific binding on antibodies and amino acid sites in a human chromogranin A amino acid sequence; the amino acid sites comprise: 1st to 113rd sites, 131st to 143rd sites, 337th to 364th sites and 373rd to 439th sites; the detection reagent can be used for quantitatively detecting the concentration of chromograninA in human blood plasma and is clinically mainly used for auxiliary diagnosis and differential diagnosis on pheochromocytoma and neuroendocrine neoplasm; the reference interval of the invention has ahigh conformity degree with clinical diagnosis, and the accuracy of the auxiliary diagnosis is improved; a detection method developed by a full-automatic magnetic bead chemiluminescence platform is further utilized by the invention and the detection period is shortened.

Description

technical field [0001] The invention belongs to the field of reagent diagnosis research, in particular to a chromogranin A detection reagent, a detection reference interval and a detection method. Background technique [0002] Chromogranin A or chromogranin A (CGA) belongs to the chromogranin protein family. Chromogranin exists in the secretory vesicles of all neuroendocrine cells that can secrete catecholamines or other endocrine hormones, and is rich in acidic amino acids. Acidic soluble protein, originally extracted from bovine adrenal medulla granules, was found to widely exist in the nervous system and APUD (amine precursor uptake and decarboxylation) system. cDNA sequence analysis and biochemical research show that CGA is composed of 439 amino acid residues, its molecular weight is 48KD, its isoelectric point is 4.8, and it has the characteristics of heat deformation resistance. [0003] As a precursor peptide, CGA can be decomposed into different fragments in differe...

Claims

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Application Information

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IPC IPC(8): G01N33/68G01N33/543
CPCG01N33/54326G01N33/6803
Inventor 高平
Owner EPITOPE BIOTECH
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