AQP2 (p-S264/261) Rabbit pAb, AP conj.(bs-4610R-AP)-100ul产品图

AQP2 (p-S264/261) Rabbit pAb,

AP conj.(bs-4610R-AP)-100ul
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  • bs-4610R-AP
  • 2026年10月14日
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    • 规格:

      100ul

    产品编号bs-4610R-AP
    英文名称phospho-AQP2 (Ser264+261) Rabbit pAb, AP conjugated
    中文名称AP标记的磷酸化水通道蛋白2抗体
    英文别名Aquaporin 2(phospho S261); p-Aquaporin 2(phospho S261) ADH water channel; AQP 2; AQP CD; AQP2; AQPCD; Aquaporin 2 collecting duct; Aquaporin CD; Aquaporin2; Aquaporine 2; Collecting duct water channel protein; MGC34501; Water channel protein for renal collecting duct; WCH CD; WCHCD.
    产品应用WB=1:500-2000

    Not yet tested in other applications.
    Optimal working dilutions must be determined by the end user.

    抗体来源Rabbit
    免疫原KLH conjugated synthesised phosphopeptide derived from human AQP2 around the phosphorylation site of Ser264/261
    亚型IgG
    纯化方法affinity purified by Protein A
    克隆类型Polyclonal
    浓度1mg/ml
    储存液0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
    研究领域

    Signal Transduction > Metabolism > Plasma Membrane > Channels

    亚细胞定位Apical cell membrane; Multi-pass membrane protein. Cytoplasmic vesicle membrane; Multi-pass membrane protein. Note=Shuttles from vesicles to the apical membrane.
    组织特异性Expressed in renal collecting tubules.
    翻译后修饰Ser-256 phosphorylation is necessary and sufficient for expression at the apical membrane. Endocytosis is not phosphorylation-dependent.
    相似性Belongs to the MIP/aquaporin (TC 1.A.8) family.
    功能Forms a water-specific channel that provides the plasma membranes of renal collecting duct with high permeability to water, thereby permitting water to move in the direction of an osmotic gradient.
    保存条件Shipped at 4℃. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    注意事项This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    背景资料This gene encodes a water channel protein located in the kidney collecting tubule. It belongs to the MIP/aquaporin family, some members of which are clustered together on chromosome 12q13. Mutations in this gene have been linked to autosomal dominant, and recessive forms of nephrogenic diabetes insipidus. Belongs to the MIP/aquaporin (TC 1.A.8) family.

     

    应用推荐稀释比例
    {WB}{1:500-2000}

     

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