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

CBPD0004

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索取COA
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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 
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

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