α-thalassemia αα/--SEA Reference Standard
CBPD0029
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產品描述
產品數據庫
| Introduction | |
| Format | Genomic DNA |
| Description | a-thalassemia is the most common human monogenic hereditary diseases in theworld. Generally, a-thalassemia is mainly resulted from a-globin gene defects whichlocated in 16p13.3. a-thalassemia is classified as deletional or non-deletional accordingto the mutational.The most common mutation producing this syndrome is the Southeast Asian (- SEA ) double -globin gene deletion mechanism involved. |
| Technical Data | |
| Mutation information | Variation site: N/A |
| Zygosity: Heterozygous | |
| Allelic Frequency: 50% | |
| Transcript | N/A |
| Chr position(GRCh37) | chr16:215396-234699 del |
| 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 |
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| Storage | 2-8℃ |
| Expiry | 36 months from the date of manufacture |
