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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 | |
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 | 2-8℃ |
Expiry | 36 months from the date of manufacture |