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  4. ATP6V1B2 Antibody

ATP6V1B2 Antibody

  • 中文名稱：
    ATP6V1B2兔多克隆抗體
  • 貨號：
    CSB-PA002398ESR1HU
  • 規格：
    ￥440
  • 圖片：
    • Western blot
      All lanes: ATP6V1B2 antibody at 5µg/ml + Hela whole cell lysate
      Secondary
      Goat polyclonal to rabbit IgG at 1/10000 dilution
      Predicted band size: 57 kDa
      Observed band size: 57 kDa
  • 其他：

產品詳情

  • 產品名稱：
    Rabbit anti-Homo sapiens (Human) ATP6V1B2 Polyclonal antibody
  • Uniprot No.：
  • 基因名：
  • 別名：
    ATP6B1B2 antibody; ATP6B2 antibody; ATP6V1 B2 antibody; ATP6V1B 2 antibody; ATP6V1B2 antibody; ATPase H+ transporting lysosomal 56/58kDa V1 subunit B isoform 2 antibody; ATPase H+ transporting lysosomal 56/58kDa V1 subunit B2 antibody; ATPase H+ transporting, lysosomal (vacuolar proton pump) beta polypeptide 56/58kD isoform 2 antibody; ATPase, H+ transporting, lysosomal V1 subunit B2 antibody; brain isoform antibody; Endomembrane proton pump 58 kDa subunit antibody; H+ transporting two sector ATPase antibody; HO 57 antibody; HO57 antibody; V ATPase B2 subunit antibody; V ATPase subunit B 2 antibody; V type proton ATPase subunit B, brain isoform antibody; V-ATPase subunit B 2 antibody; V-type proton ATPase subunit B antibody; Vacuolar ATP synthase subunit B brain isoform antibody; Vacuolar H+ ATPase 56,000 subunit antibody; Vacuolar H+ ATPase 56000 subunit antibody; Vacuolar H+ATPase B2 antibody; Vacuolar proton pump subunit B 2 antibody; VAT B2 antibody; VATB 2 antibody; VATB antibody; VATB2 antibody; VATB2_HUMAN antibody; Vma 2 antibody; Vma2 antibody; VPP 3 antibody; VPP3 antibody
  • 宿主：
    Rabbit
  • 反應種屬：
    Human
  • 免疫原：
    Recombinant Human V-type proton ATPase subunit B, brain isoform protein (262-511AA)
  • 免疫原種屬：
    Homo sapiens (Human)
  • 標記方式：
    Non-conjugated
  • 克隆類型：
    Polyclonal
  • 抗體亞型：
    IgG
  • 純化方式：
    Antigen Affinity Purified
  • 濃度：
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液：
    PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
  • 產品提供形式：
    Liquid
  • 應用范圍：
    ELISA, WB
  • 推薦稀釋比：
    Application Recommended Dilution
    WB 1:1000-1:5000
  • Protocols：
  • 儲存條件：
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 貨期：
    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.
  • 用途：
    For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產品評價

靶點詳情

  • 功能：
    Non-catalytic subunit of the V1 complex of vacuolar(H+)-ATPase (V-ATPase), a multisubunit enzyme composed of a peripheral complex (V1) that hydrolyzes ATP and a membrane integral complex (V0) that translocates protons. V-ATPase is responsible for acidifying and maintaining the pH of intracellular compartments and in some cell types, is targeted to the plasma membrane, where it is responsible for acidifying the extracellular environment. In renal intercalated cells, can partially compensate the lack of ATP6V1B1 and mediate secretion of protons (H+) into the urine under base-line conditions but not in conditions of acid load.
  • 基因功能參考文獻：
    1. We conclude that the effects of variation in the vacuolar ATPase may point to a new molecular mechanism that influences the long-term development of depression. This mechanism may involve dysfunction specifically in hippocampal circuitry and cognitive impairment that characterizes recurrent and chronic depression. PMID: 27824360
    2. ATP6V1B2 is somatically mutated in 22% of follicular lymphoma tumors. Mutation hotspots found at Y371 and R400. PMID: 25713363
    3. A missense mutation in ATP6V1B2 associated with Zimmermann-Laband syndrome. PMID: 25915598
    4. The ATP6V1B2 p.Arg506X is a haploinsufficient mutation and resulted in abnormal acidification in lysosomes. PMID: 24913193
    5. This protein has been found differentially expressed in the anterior cingulate cortex from patients with schizophrenia PMID: 20381070

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  • 相關疾病：
    Zimmermann-Laband syndrome 2 (ZLS2); Deafness, congenital, with onychodystrophy, autosomal dominant (DDOD)
  • 亞細胞定位：
    Apical cell membrane. Melanosome. Cytoplasm.
  • 蛋白家族：
    ATPase alpha/beta chains family
  • 組織特異性：
    Kidney; localizes to early distal nephron, encompassing thick ascending limbs and distal convoluted tubules (at protein level).
  • 數據庫鏈接：

    HGNC: 854

    OMIM: 124480

    KEGG: hsa:526

    STRING: 9606.ENSP00000276390

    UniGene: Hs.295917



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