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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-I-110(G>A) double mutation Reference Standard

β-thalassemia Codon 39(C>T)&IVS-I-110(G>A) double mutation Reference Standard

CBPD0001

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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-I-110(G>A)
	DNA Change: c.93-21G>A
	Zygosity: Heterozygous
	Allelic Frequency: 50%
	Chr position(GRCh37): Chr11:5248050C>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-I-110(G>A) Heterozygous
Storage	2-8℃
Expiry	36 months from the date of manufacture

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