Gene ID (NCBI) 6572 Alternative Names SLC18A3; CMS21; VACHT; solute carrier family 18 member A3 Application Notes: The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user. ...
CDS-R08656-1 pDonR223-SLC18A3 GateWay 2ug/0.5ml ￥0 现货 CDS-R08656-2 pMD18-T-SLC18A3 TA克隆 2ug/0.5ml ￥0 1-2周SLC18A3 重组腺病毒 货号产品名称Method规格价格货期 CDS-R08656-11 rAd-SLC18A3 重组过表达腺病毒 10^10 vg/支 ￥2500 3-5周 CDS-R08656-12 rAd-sh-SLC18A3 重组干扰...
Our investigations revealed a homozygous nonsense variant [c.1116C A, p.(Cys372Ter)] in the SLC18A3 gene, which encodes for the vesicular acetylcholine transporter (VAChT) responsible for active transport of acetylcholine in the neuromuscular junction. This is the first description of a nonsense ...
中文名称:Anti-SLC18A3 Polyclonal Antibody英文名称:Anti-SLC18A3 Polyclonal Antibody Gene ID:6572Public Immunogen Range:A synthetic peptide of human SLC18A3 Subcellular Locations:MembraneSwiss Prot:Q16572 保存:Store at -20°C. Avoid freeze / thaw cycles.别名:VACHT ...
Immunogen Recombinant protein of human SLC18A3 Calculated molecular weight 56kDa Observed molecular weight Refer to figures Swiss Prot Q16572 Gene ID (NCBI) 6572 Alternative Names SLC18A3; CMS21; VACHT; solute carrier family 18 member A3 Application Notes: The application notes include recommended...
Rabbit Polyclonal Antibody to SLC18A3 别名: VACHT 应用: 反应种属: Human Description This gene is a member of the vesicular amine transporter family. The encoded transmembrane protein transports acety
This is the first description of a nonsense variant in the SLC18A3 gene, as only missense variants and whole gene deletions have been previously identified in patients. The previously detected SLC18A3 defects have been associated with congenital myasthenic syndromes, and therefore our findings extend...