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VRK1 (1F6) Mouse mAb

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2026年01月04日
  • W
  • H
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      VRK1 (1F6) Mouse mAb

    • 抗原

      recombinant fusion protein GST-full length human VRK1

    • 应用范围

      W

    • 供应商

      CST

    • 保质期

      详见说明书

    • 级别

      详见MSDS文件

    • 适应物种

      H

    • 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

    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) Isotype
    W H Endogenous 48 Mouse IgG1
    Protocols
    Specificity / Sensitivity

    VRK1 (1F6) Mouse mAb detects endogenous levels of total VRK1 protein.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with recombinant fusion protein GST-full length human VRK1.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from 293 and HeLa cells using VRK1 (1F6) Mouse mAb.

    Background

    The vaccinia-related kinase (VRK) proteins are a new group of Ser/Thr kinases in the human kinome. This mammalian kinase family comprises three members, VRK1, VRK2, and VRK3 (1-3). The VRK1 has autophosphorylation activity and phosphorylates several transcription factors, including p53 (4), ATF2 (5), and c-Jun (6). VRK2 is associated with the endoplasmic reticulum (7). VRK3 suppresses Erk activity through direct interaction and activation of the MAP kinase phosphatase VHR (8). Further functional and structural analysis of VRK proteins will elucidate important new aspects of cell regulation.

    1. Nezu, J. et al. (1997) Genomics 45, 327-31.
    2. Zelko, I. et al. (1998) Arch Biochem Biophys 352, 31-6.
    3. Vega, F.M. et al. (2003) FEBS Lett 544, 176-80.
    4. Lopez-Borges, S. and Lazo, P.A. (2000) Oncogene 19, 3656-64.
    5. Sevilla, A. et al. (2004) J Biol Chem 279, 27458-65.
    6. Sevilla, A. et al. (2004) Oncogene 23, 8950-8.
    7. Nichols, R.J. and Traktman, P. (2004) J Biol Chem 279, 7934-46.
    8. Kang, T.H. and Kim, K.T. (2006) Nat Cell Biol 8, 863-9.
    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
    • Purification of mAb (IgG)

      (adjust pH to 7.8 with Binding buffer; red color) to the Protein A column.Mouse antibodies of the IgG1 subclass do not have a high affinity for protein A. Purification on protein A beads using standard conditions will yield approximately 1/10

    • Purification of mAb (IgG)

        Purification of mAb (IgG) by Chang-Duk Jun, 03/14/2000 Purpose Materials Antibody 7E3 , 2L sup grown in flasks, frozen and thawed overnight. BioRad Affi-Gel Protein A MAPS II Buffers

    • T-Cell Activation Using mAb to CD3

      One of the most common ways to assess T cell activation is to measure T cell proliferation upon in vitro stimulation of T cells via antigen or agonistic antibodies to TCR. This protocol is written as a starting point for examining in vitro proliferation of mouse

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