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ABSTRACT: Objective
The aim of the present study is to develop and validate a reliable and simple application for genotyping serum amyloid A1 (SAA1).Methods
The specific nested PCR was performed to amplify a product of SAA1 gene. Two quenching probes (QPs) were designed for detecting two single nucleotide polymorphism (SNP) sites, rs1136743(C/T) and rs1136747(C/T) respectively for SAA1 genotypes. The specific nested PCR and QPs of SAA1 genotying was introduced into a fully automated genotyping system (I-densy, ARKRAY, Inc.), which enables the genotyping of SAA1 from whole blood.Results
Six genotypes of SAA1 (α+/+, β+/+, γ+/+, αβ, αγ and βγ) could be determined by monitoring the fluorescence intensity o
SUBMITTER: Zhang J
PROVIDER: S-EPMC8100075 | biostudies-literature | 2021 Apr
REPOSITORIES: biostudies-literature