ATP6V1H Antibody
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货号:CSB-PA004431
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规格:¥880
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图片:
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其他:
产品详情
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Uniprot No.:Q9UI12
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基因名:
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别名:Atp6v1h antibody; ATPase; H+ transporting; lysosomal 50/57kDa; V1 subunit H antibody; CGI 11 antibody; CGI11 antibody; EC 3.6.3.14 antibody; MSTP042 antibody; NBP1 antibody; Nef binding protein 1 antibody; Nef-binding protein 1 antibody; Protein VMA13 homolog antibody; SFD antibody; SFDalpha antibody; SFDbeta antibody; V ATPase subunit H antibody; V-ATPase 50/57 kDa subunits antibody; V-ATPase subunit H antibody; V-type proton ATPase subunit H antibody; Vacuolar ATP synthase subunit H antibody; Vacuolar proton pump subunit H antibody; Vacuolar proton pump subunit SFD antibody; VATH_HUMAN antibody; VMA13 antibody
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宿主:Rabbit
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反应种属:Human,Mouse
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免疫原:Synthesized peptide derived from the Internal region of Human V-ATPase H.
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免疫原种属:Homo sapiens (Human)
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标记方式:Non-conjugated
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抗体亚型:IgG
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纯化方式:The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
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浓度:It differs from different batches. Please contact us to confirm it.
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保存缓冲液:Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
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产品提供形式:Liquid
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应用范围:WB, IHC, ELISA
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推荐稀释比:
Application Recommended Dilution WB 1:500-1:2000 IHC 1:100-1:300 ELISA 1:20000 -
Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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货期:Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
相关产品
靶点详情
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功能:Subunit of the peripheral V1 complex of vacuolar ATPase. Subunit H activates the ATPase activity of the enzyme and couples ATPase activity to proton flow. Vacuolar ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells, thus providing most of the energy required for transport processes in the vacuolar system. Involved in the endocytosis mediated by clathrin-coated pits, required for the formation of endosomes.
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基因功能参考文献:
- These data provide evidence that partial loss of ATP6V1H function results in osteoporosis/osteopenia. PMID: 27924156
- These studies have uncovered a new, ATP6V1H-mediated pathway that regulates bone formation, and defines a new mechanism of disease that leads to bone loss. We propose that MMP9/MMP13 could be therapeutic targets for patients with this rare genetic disease. PMID: 28158191
- ATP6V1H may represent a critical molecular mechanism involved in the development of type 2 diabetes and its compilations through its important regulatory effect on vacuolar-ATPase activity. PMID: 21871445
- Our study shows that multiple mechanisms of pump dysfunction result from B1 subunit mutations with a common outcome being defective assembly PMID: 18368028
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蛋白家族:V-ATPase H subunit family
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组织特异性:Widely expressed.
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数据库链接:
HGNC: 18303
OMIM: 608861
KEGG: hsa:51606
STRING: 9606.ENSP00000352522
UniGene: Hs.491737
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