A gilbert syndrome gene mutation detection kit

A detection kit and syndrome technology, applied in the field of Gilbert syndrome gene mutation detection kits, can solve the problems of expensive sequencing and other problems
CN104805199BActive Publication Date: 2017-12-29吴旭平
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Patent Information

Authority / Receiving Office
CN · China
Patent Type
Patents(China)
Current Assignee / Owner
吴旭平
Publication Date
2017-12-29

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Abstract

The invention relates to a gene mutation detection kit for the GS (Gilbert syndrome) and belongs to the technical field of biology. The kit comprises DNA (deoxyribose nucleic acid) micro-array chips formed by fixing an acrylamide modified PCR (polymerase chain reaction) product and other components on a propylene group modified slide as well as 6 nucleotide probe parts. The kit adopts a DNA micro-array technology, is simple and convenient to operate, low in price and capable of being applied to screening and clinical auxiliary diagnosis of diseases related to the GS caused by gene mutation.
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Description

technical field

[0001] The invention relates to a gene detection kit, in particular to a Gilbert syndrome gene mutation detection kit, which belongs to the field of biotechnology. Background technique

[0002] Gilbert syndrome (Gilbert syndrome, GS), first reported by Gilbert and Lereboullet in 1901, also known as constitutional dyshepatic jaundice, is a common hereditary unconjugated bilirubinemia. Patients with this disease have jaundice due to the dysfunction of hepatic uptake of unconjugated bilirubin (unconjugated bilirubin, UCB) and the insufficiency of glucuronosyltransferase (uridine diphosphate glucuronosyl transferase, UGT) in microsomes, resulting in increased blood UCB. Patients mainly present with non-hemolytic intermittent jaundice mainly caused by elevated indirect bilirubin, and some patients may experience fatigue, dyspepsia, liver discomfort, and fat intolerance.

[0003] With the development of molecular biology techniques, the research on Gilbert syndrom...

Claims

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