名稱 | β-thalassemia mutation Reference Standard Ⅰ |
型號(hào) | CBPD0001 |
報(bào)價(jià) | |
特點(diǎn) | β-thalassemia mutation Reference Standard Ⅰ |
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聯(lián)系人:蔣經(jīng)理
電話:4008750250
號(hào)碼:
手機(jī):18066071954
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Email: zhangxiangwen@cobioer.com
電話:4008750250
號(hào)碼:
手機(jī):18066071954
地址:南京市棲霞區(qū)緯地路9號(hào)
Email: zhangxiangwen@cobioer.com
產(chǎn)品展示 / PRODUCTS
基因檢測(cè)標(biāo)準(zhǔn)品 > 地中海貧血標(biāo)準(zhǔn)品 > CBPD0001β-thalassemia mutation Reference Standard Ⅰ
- 詳細(xì)內(nèi)容
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 | 4℃ |
Expiry | 36 months from the date of manufacture |