名稱 |
β-thalassemia mutation Reference Standard Ⅱ |
型號 |
CBPD0002 |
報價 |
 |
特點 |
β-thalassemia mutation Reference Standard Ⅱ |
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 | IVS-I-110(G>A) |
DNA Change | c.93-21G>A |
Zygosity | Homozygous |
Allelic Frequency | 100% |
Transcript | NM_000518.5 |
Chr position(GRCh37) | Chr11:5248050C>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. IVS-I-110(G>A) Homozygous |
Storage | 4℃ |
Expiry | 36 months from the date of manufacture |
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