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科研细胞
药靶细胞
标准品
NGS靶向捕获探针
AI-Edigene® SLC26A4 p.H723R Reference Standard Plus
CBPD0026
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Format | Genomic DNA |
Description | SLC26A4 (Solute Carrier Family 26 Member 4) is a Protein Coding gene. Diseases associated with SLC26A4 include Pendred Syndrome and Deafness, Autosomal Recessive 4, With Enlarged Vestibular Aqueduct. Among its related pathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Disorders of transmembrane transporters. |
Technical Data | |
DNA Change | c.2168A>G |
AA Change | p.H723R |
Zygosity | Homozygous |
Allelic Frequency | 100% |
Chr position (GRCh38) | chr7: 107710132 |
Transcript | NM_000441.2 |
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 | |
Storage | 4°C |
Expiry | 36 months from the date of manufacture |
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