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基因檢測標準品 > 地中海貧血標準品 > CBPD0003β-thalassemia mutation Reference Standard Ⅲ

β-thalassemia mutation Reference Standard Ⅲ
名稱 β-thalassemia mutation Reference Standard Ⅲ
型號 CBPD0003
報價
特點 β-thalassemia mutation Reference Standard Ⅲ
  • 詳細內容
Introduction
FormatGenomic DNA
Descriptionβ-thalassemia (β-mediterraneananemia) refers to the A group of hemoglobinopathies in which synthesis is partially or completely inhibited.
  
Technical Data 
Mutation 1Variation site: -87(C>G)
DNA Change: N/A
Zygosity: Heterozygous
Allelic Frequency: 50%
Chr position(GRCh37): Chr11.5248388C>G
Transcript: NM_000518.5
Mutation 2Variation site: IVS-I-110(G>A)
DNA Change: c.93-21G>A
Zygosity: Homozygous
Allelic Frequency: 100%
Chr position(GRCh37): Chr11.5248050C>T
Transcript: NM_000518.5
BufferTris-EDTA
  
Product Information 
Intended UseResearch Use Only
Unit Size1ug
ConcentrationDownload for COA
PuroficationDownload for COA
DNA electrophoresisDownload for COA
Sanger sequencing

β-thalassemia mutation Reference Standard Ⅲ

Figure 1. -87(C>G) Heterozygous

β-thalassemia mutation Reference Standard Ⅲ

Figure 2. IVS-I-110(G>A) Homozygous

Storage4℃
Expiry36 months from the date of manufacture


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