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GRK6 (D1A4) Rabbit mAb

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年12月02日
  • W
  • H,M,R
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      GRK6 (D1A4) Rabbit mAb

    • 抗原

      synthetic peptide corresponding to residues surrounding Glu89 of human GRK6 protein

    • 应用范围

      W

    • 适应物种

      H,M,R

    • 供应商

      CST

    • 保质期

      详见说明书

    • 级别

      详见MSDS文件

    • 库存

      大量

    • 是否单克隆

      1

    • 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

    more info application references datasheet PDF MSDS PDF protocols

    Applications Key:  W=Western Blotting
    Reactivity Key:  H=Human  M=Mouse  R=Rat
    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) Isotype
    W H M R Endogenous 70 Rabbit IgG
    Protocols
    Specificity / Sensitivity

    GRK6 (D1A4) Rabbit mAb recognizes endogenous levels of total GRK6 protein.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Glu89 of human GRK6 protein.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from various cell lines using GRK6 (D1A4) Rabbit mAb.

    Background

    G protein-coupled R eceptor K inase 6 (GRK6) is one of 7 members of the GRK serine/threonine kinase subfamily, which are known primarily for their role in desensitizing activated G protein-coupled receptors (GPCRs) (1,2). GRKs function by phosphorylating serine/threonine residues in activated GPCRs. Upon phosphorylation these residues serve as binding sites for β-arrestin proteins, inhibiting re-activation of GPCRs by blocking their re-association with G proteins (3). There is evidence that GRKs can also modulate selected non-GPCR signaling pathways (2). For example, GRK6 has been shown to modulate the Wnt signaling pathway via phosphorylation of LRP6 (4), and the insulin-like growth factor signaling pathway (5). GRK6 may also play a role in immune system function. Investigators have found GRK6 expression is typically abundant in hematopoietic tumor cell lines, and a recent research study demonstrated that GRK6 suppression was selectively lethal for a number of myeloma tumor cell lines (6).

    1. Mushegian, A. et al. (2012) PLoS One 7, e33806.
    2. Gurevich, E.V. et al. (2012) Pharmacol Ther 133, 40-69.
    3. Ribas, C. et al. (2007) Biochim Biophys Acta 1768, 913-22.
    4. Chen, M. et al. (2009) J Biol Chem 284, 35040-8.
    5. Zheng, H. et al. (2012) Proc Natl Acad Sci U S A 109, 7055-60.
    6. Tiedemann, R.E. et al. (2010) Blood 115, 1594-604.
    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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    图标文献和实验
    相关实验
    • Methods for the Detection of D-Amino-Acid Oxidase

      then twice for 5 min. It was incubated for 1 hr in TBS-T containing rabbit anti-hog D-amino-acid oxidase IgG (1/3,000 dilution) and quickly rinsed twice with TBS-T and further washed in TBS-T once for 15 min then twice for 5 min. The membrane was incubated

    • 组化染色背景高?没信号?一篇文章带你快速掌握免疫组化!

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    • Methods for the Detection of D-Amino-Acid Oxidase

      min then twice for 5 min. It was incubated for 1 hr in TBS-T containing rabbit anti-hog D-amino-acid oxidase IgG (1/3,000 dilution) and quickly rinsed twice with TBS-T and further washed in TBS-T once for 15 min then twice for 5 min. The membrane

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