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β-thalassemia IVS-II-654(C>T)&IVS-II-654(C>T) double mutation Reference Standard

CBPD0007

询价

索取COA

产品描述

产品数据库

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: CD71-72(+A)
	DNA Change: c.216_217insA
	Zygosity: Heterozygous
	Allelic Frequency: 50%
	Chr position(GRCh37): Chr11:5247905_5247906 insA
	Transcript: NM_000518.5
Mutation 2	Variation site: IVS-II-654(C>T)
	DNA Change: c.316-197C>T
	Zygosity: Heterozygous
	Allelic Frequency: 50%
	Chr position(GRCh37): Chr11:5247153C>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 71/72(+A) Heterozygous Figure 2. IVS-II-654(C>T) Heterozygous
Storage	2-8℃
Expiry	36 months from the date of manufacture

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