名稱 | β-thalassemia mutation Reference Standard Ⅳ |
型號(hào) | CBPD0004 |
報(bào)價(jià) | ![]() |
特點(diǎn) | β-thalassemia mutation Reference Standard Ⅳ |
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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
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基因檢測(cè)標(biāo)準(zhǔn)品 > 地中海貧血標(biāo)準(zhǔn)品 > CBPD0004β-thalassemia mutation Reference Standard Ⅳ

- 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 | |
Variation site | Codon 6(A>T) |
DNA Change | c.20A>T |
Zygosity | Heterozygous |
Allelic Frequency | 50% |
Transcript | NM_000518.5 |
Chr position(GRCh37) | Chr11:5248232A>T |
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 6(A>T) Heterozygous |
Storage | 4℃ |
Expiry | 36 months from the date of manufacture |