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

CBPD0005

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索取COA

產(chǎn)品描述

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