Dysbindin Antibody

Dysbindin Antibody

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年10月16日
  • W
  • Rabbit
  • H
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    • 详细信息
    • 技术资料
    • 抗体英文名

      Dysbindin Antibody

    • 抗原

      synthetic peptide corresponding to human dysbindin

    • 应用范围

      W

    • 宿主

      Rabbit

    • 供应商

      CST

    • 适应物种

      H

    • 级别

      详见MSDS文件

    • 库存

      大量

    • 保质期

      详见说明书

    • 是否单克隆

      2

    • 保存条件

      -20°c

    • 规格

      100 ul (10 western blots)/carrier free & custom formulation / quantity

    规格:产品价格:¥请询价
    规格:100 ul (10 western blots)产品价格:¥请询价
    规格:carrier free & custom formulation / quantity产品价格:¥请询价

    pathway more info application references datasheet PDF MSDS PDF protocols

    Applications Key:  W=Western Blotting
    Reactivity Key:  H=Human
    Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

    Applications Reactivity Sensitivity MW (kDa) Source
    W H Endogenous 50 Rabbit
    Protocols
    Specificity / Sensitivity

    Dysbindin Antibody detects endogenous levels of total dysbindin protein.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to human dysbindin. Antibodies are purified by peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of HeLa cells, untransfected or transfected with a construct overexpressing dysbindin, and other cell lines using Dysbindin Antibody.

    Background

    Dysbindin, or dystrobrevin-binding protein 1, is a coiled-coil-containing protein expressed in muscle and brain that was identified as a binding partner of dystrobrevin (1). Dysbindin upregulates expression of the pre-synaptic proteins SNAP25 and synapsin I, thereby increasing glutamate release and promoting neuronal viability through Akt signaling. In particular, Akt phosphorylation is suppressed with downregulation of dysbindin and increased with upregulation of dysbindin (2). A nonsense mutation of dysbindin causes Hermansky-Pudlak disease, an autosomal recessive disorder characterized by lysosomal storage defects and prolonged bleeding. (2). Genetic variation in the gene encoding dysbindin is strongly associated with schizophrenia and protein levels are reduced in the prefrontal cortex, midbrain and hippocampus of brains from patients with schizophrenia (3,4).

    1. Benson, M.A. et al. (2001) J Biol Chem 276, 24232-41.
    2. Numakawa, T. et al. (2004) Hum Mol Genet 13, 2699-708.
    3. Straub, R.E. et al. (2002) Am J Hum Genet 71, 337-48.
    4. Talbot, K. et al. (2004) J Clin Invest 113, 1353-63.
    Application References

    Have you published research involving the use of our products? If so we'd love to hear about it. Please let us know !

    Companion Products

    For Research Use Only. Not For Use In Diagnostic Procedures.

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