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