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β-thalassemia Codon 6(A>T) mutation Reference Standard

CBPD0004

詢 價
索取COA
產(chǎn)品描述
產(chǎn)品數(shù)據(jù)庫
Introduction
Format Genomic DNA
Description β-thalassemia (β-mediterraneananemia) refers to the A group of hemoglobinopathies in which synthesis is partially or completely inhibited.
   
Technical Data 
Variation site Codon 6(A>T)
DNA Change c.20A>T
Zygosity Heterozygous
Allelic Frequency 50%
Transcript NM_000518.5
Chr position(GRCh37) Chr11:5248232A>T
Buffer Tris-EDTA
   
Product Information 
Intended Use Research Use Only
Unit Size 1ug
Concentration Download for COA
Purofication Download for COA
DNA electrophoresis Download for COA
Sanger sequencing

Figure 1. Codon 6(A>T) Heterozygous

Storage 2-8℃
Expiry 36 months from the date of manufacture

藥靶模型聯(lián)系方式: 華東銷售經(jīng)理:18240630236 全國銷售經(jīng)理:18066071954
診斷標準品聯(lián)系方式: 華東銷售經(jīng)理:15000320447 華北銷售經(jīng)理:18131625521 華南銷售經(jīng)理:13484295986 華中&西南銷售經(jīng)理:13871580511 全國銷售經(jīng)理:13484295986

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