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首頁 /診斷試劑 /遺傳性基因標(biāo)準(zhǔn)品 /地中海貧血 /β-thalassemia Codon 39(C>T)&IVS-II-1(G>A) double mutation Reference Standard

β-thalassemia Codon 39(C>T)&IVS-II-1(G>A) double mutation Reference Standard

CBPD0005

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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 
Mutation 1 Variation site: Codon 39(C>T)
DNA Change: c.118C>T
Zygosity: Heterozygous
Allelic Frequency: 50%
Chr position(GRCh37): Chr11:5248004G>A
Transcript: NM_000518.5
Mutation 2 Variation site: IVS-II-1(G>A)
DNA Change: c.315+1G>A
Zygosity: Heterozygous
Allelic Frequency: 50%
Chr position(GRCh37): Chr11:5247806C>T
Transcript: NM_000518.5
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 39(C>T) Heterozygous

Figure 2. IVS-II-1(G>A) Heterozygous

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

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藥靶模型聯(lián)系方式: 華東銷售經(jīng)理(上海):18240630236 華東銷售經(jīng)理(上海、江蘇、安徽):15715191010 華中&華西銷售經(jīng)理:18071545918 華中&西南銷售經(jīng)理:13871580511 華北銷售經(jīng)理:18628311252 全國(guó)銷售經(jīng)理:13816461235
診斷標(biāo)準(zhǔn)品聯(lián)系方式: 華東銷售經(jīng)理:15000320447 華北銷售經(jīng)理:18628311252 華中&華西銷售經(jīng)理:18071545918 華中&西南銷售經(jīng)理:13871580511 全國(guó)銷售經(jīng)理:13816461235

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