CA VIII Polyclonal Antibody

活动价:

¥680.00

市场价:¥880.00

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产品规格:
  • 50μL
  • 100μL
货号:

FAB2613110

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商品描述
  • 靶点-Target

    CA VIII

  • 反应性

    Human,Mouse,Rat

  • 应用

    WB,IHC,IF,ELISA

  • 宿主物种-Host Species

    Rabbit

  • 同种型-Isotype

    IgG

  • 修饰-Modification

    Unmodified

  • MW(Calculated)

    33kD

  • 推荐稀释比

    IHC: 100-300;WB 1:500-1:2000;ELISA 1:40000;IF 1:50-200

  • 组成

    Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

  • 纯化工艺

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

  • 储存

    -15°C to -25°C/1 year(Do not lower than -25°C)

  • 浓度

    1 mg/ml

  • 克隆性

    Polyclonal

  • 免疫原

    Synthesized peptide derived from the Internal region of human CA VIII.

  • 特异性

    CA VIII Polyclonal Antibody detects endogenous levels of CA VIII protein.

  • 基因名称

    CA8

  • 蛋白名称

    Carbonic anhydrase-related protein

  • 别名

    CA8;CALS;Carbonic anhydrase-related protein;CARP;Carbonic anhydrase VIII;CA-VIII

  • Organism-1

    Human

  • 基因ID-1

    767

  • SwissProt-1

    P35219

  • Organism-2

    Mouse

  • 基因ID-2

    12319

  • SwissProt-2

    P28651

  • Organism-3

    Rat

  • 基因ID-3

    297814

  • SwissProt-3

    Q5PPN4

  • 背景

    The protein encoded by this gene was initially named CA-related protein because of sequence similarity to other known carbonic anhydrase genes. However, the gene product lacks carbonic anhydrase activity (i.e., the reversible hydration of carbon dioxide). The gene product continues to carry a carbonic anhydrase designation based on clear sequence identity to other members of the carbonic anhydrase gene family. The absence of CA8 gene transcription in the cerebellum of the lurcher mutant in mice with a neurologic defect suggests an important role for this acatalytic form. Mutations in this gene are associated with cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 (CMARQ3). Polymorphisms in this gene are associated with osteoporosis, and overexpression of this gene in osteosarcoma cells suggests an oncogenic role. Alternative splicing results in multiple transcript variants. [provid

  • 细胞定位

    cytoplasm,