• merck millipore,默克密理博,AB3071,Anti-Aquaporin 0 Antibody
  • merck millipore,默克密理博,AB3071,Anti-Aquaporin 0 Antibody

    产品名称:Anti-Aquaporin 0 Antibody
    产品型号:AB3071
    Detect Aquaporin 0 using this Anti-Aquaporin 0 Antibody validated for use in ELISA & WB.

    merck millipore,默克密理博,AB3071,Anti-Aquaporin 0 Antibody

  • 产品介绍
  • merck millipore,默克密理博,AB3071,Anti-Aquaporin 0 Antibody

    重要规格表

    品种反应性 主要应用 宿主 格式 抗体类型
    HWB, ELISARbAffinity PurifiedPolyclonal Antibody
    描述
    产品目录编号 AB3071
    品牌系列 Chemicon®
    商名
    • Chemicon
    描述 Anti-Aquaporin 0 Antibody
    Alternate Names
    • Major Intrinsic Protein
    • AQP0
    • MIP
    产品信息
    格式 Affinity Purified
    演示 Affinity purified immunoglobulin. Liquid in PBS, pH 7.4 with 0.1% BSA and 0.1% sodium azide.
    应用
    应用 Detect Aquaporin 0 using this Anti-Aquaporin 0 Antibody validated for use in ELISA & WB.
    主要应用
    • Western Blotting
    • ELISA
    应用说明 We recommend the use of 0.5-1% milk in all primary/secondary dilutions in order to suppress non-specific bands.

    Western blot: 1-10 μg/mL using Chemiluminescence technique

    ELISA: 0.5-1.0 μg/mL

    Optimal working dilutions must be determined by end user.
    生物信息
    免疫原品种 A 17 AA synthetic peptide within the carboxy terminal domain of human Aquaporin-0 (Shiels et al. 1988; Kent et al. 1990; Pisano et al. 1991; Shiels et al. 1996) was selected for antibody production. This domain is predicted to be cytoplasmic.
    浓缩 Please refer to the Certificate of Analysis for the lot-specific concentration.
    宿主 Rabbit
    特异性 Water is a critical component of all living cells. Interestingly, tissue membranes show a great degree of water permeability. Mammalian red cells, renal proximal tubules, and descending thin limb of Henle are extraordinarily permeable to water. Water crosses hydrophobic plasma membranes either by simple diffusion or through a facilitative transport mechanism mediated by special protein "aquaporin". Over the last decade, genes for several members of aquaporin family have been cloned, expressed, and their distribution studied in many tissues. Aquaporin-0 or MIP26 (major intrinsic protein 26 kDa), and Aquaporin-1 (purified from red cells) also called CHIP-28 (channel forming integral protein, 28 kDa; 268 AA; gene locus 7p14) has been the foundation of the growing family of aquaporins. The lens specific Aquaporin-0 represents up to 80% of total lens membrane protein. Defects in MIP26 are a cause of autosomal dominant cataract. The cataract Fraser mutation (CAT-FR or Shriveled) is a transposon-induced splicing error that substitutes a long terminal repeat sequence for the c-terminus of MIP. The lens opacity mutation (LOP) is an AA substitution that inhibits targeting of MIP to the cell membrane. Human Aquaporin-0 is a 263 amino acid transmembrane protein belonging to the MIP family. Aquaporin families of proteins are predicted to contain six transmembrane domains. The N and C-terminus are predicted to be cytoplasmic.
    品种反应性 Human
    抗体类型 Polyclonal Antibody
    Entrez基因编号
    • NM_012064.2
    Entrez基因汇总 Major intrinsic protein is a member of the water-transporting aquaporins as well as the original member of the MIP family of channel proteins. The function of the fiber cell membrane protein encoded by this gene is undetermined, yet this protein is speculated to play a role in intracellular communication. The MIP protein is expressed in the ocular lens and is required for correct lens function. This gene has been mapped among aquaporins AQP2, AQP5, and AQP6, in a potential gene cluster at 12q13.
    基因符号
    • MIP26
    • MIP
    • Aquaporin-0
    • aquaporin
    • AQP0
    • LIM1
    • MP26
    UniProt编号
    • P30301
    UniProt汇总 FUNCTION: SwissProt: P30301 # Water channel. May be responsible for regulating the osmolarity of the lens.
    SIZE: 263 amino acids; 28122 Da
    SUBCELLULAR LOCATION: Membrane; Multi-pass membrane protein.
    TISSUE SPECIFICITY: Major component of lens fiber gap junctions.
    DOMAIN: SwissProt: P30301 Aquaporins contain two tandem repeats each containing three membrane-spanning domains and a pore-forming loop with the signature motif Asn-Pro-Ala (NPA).
    DISEASE:SwissProt: P30301 # Defects in MIP are a cause of autosomal recessive congenital cataract [MIM:154050].
    SIMILARITY: Belongs to the MIP/aquaporin (TC 1.A.8) family.
    产品使用声明
    使用声明
    • Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
    储存和货运信息
    存储条件 Maintain frozen at -20°C in undiluted aliquots for up to 12 months. Avoid repeated freeze/thaw cycles.
    包装信息
    数量 50 µg

    merck millipore,默克密理博,AB3071,Anti-Aquaporin 0 Antibody

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