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eIF4G2/p97 (D1A10) Rabbit mAb

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年11月26日
  • W, IP
  • H,M,R
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    • 文献和实验
    • 技术资料
    • 抗体英文名

      eIF4G2/p97 (D1A10) Rabbit mAb

    • 抗原

      synthetic peptide corresponding to the sequence of human eIF4G2/p97

    • 应用范围

      W, IP

    • 库存

      大量

    • 级别

      详见MSDS文件

    • 保质期

      详见说明书

    • 供应商

      CST

    • 适应物种

      H,M,R

    • 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  IP=Immunoprecipitation
    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 IP H M R Endogenous 97 Rabbit IgG
    Protocols
    Specificity / Sensitivity

    eIF4G2/p97 (D1A10) Rabbit mAb detects endogenous levels of total eIF4G2/p97 protein.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to the sequence of human eIF4G2/p97.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from various cell types using eIF4G2/p97 (D1A10) Rabbit mAb.

    Background

    The initiation of translation is an important biological event and a variety of factors contribute to this process. Members of the eIF4 translation initiation factor family bind to the 5' m7 GTP mRNA cap and unwind the mRNA secondary structure (1,2). The amino-terminal portion of eIF4G physically associates with eIF4E to stimulate the binding of eIF4E to the mRNA cap structure (3). eIF4G also interacts with eIF3 and eIF4A and serves as an adaptor molecule in the eIF4 complex (4). Moreover, eIF4G plays a role in internal ribosomal entry site (IRES)-mediated initiation of translation (5,6). The eIF4G family includes eIF4G1 (eIF4GI), eIF4G2 (p97, DAP5 or NAT1), and eIF4G3 (eIF4GII) (7). These factors share a homologous sequence that provides for interaction with initiation factors eIF3 and eIF4A. Both eIF4G1 and eIF4G3 are involved in cap-dependent translation, while eIF4G2 plays a role in IRES-mediated translation of some genes during cell stress (7,8).

    1. Yan, R. and Rhoads, R.E. (1995) Genomics 26, 394-398.
    2. Morley, S.J. et al. (1997) RNA 3, 1085-1104.
    3. Haghighat, A. and Sonenberg, N. (1997) J. Biol. Chem. 272, 21677-21680.
    4. De Gregorio, E. et al. (1998) RNA 4, 828-836.
    5. Ohlmann, T. et al. (1996) EMBO J. 15, 1371-1382.
    6. Borman, A.M. and Kean, K.M. (1997) Virology 237, 129-136.
    7. Henis-Korenblit, S. et al. (2002) Proc. Natl. Acad. Sci. USA 99, 5400-5405.
    8. Nevins, T.A. et al. (2003) J. Biol. Chem. 278, 3572-3579.
    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

      kidney D-amino-acid oxidase (Sigma, St. Louis, MO or Boehringer Mannheim, Germany) was used as a control. Organs, tissues, or tissue culture cells were homogenized in distilled water and centrifuged at 550 x g for 5 min. The supernatant solutions

    • 组化染色背景高?没信号?一篇文章带你快速掌握免疫组化!

      组织化学分析。(图 C)使用Anti-Erk1/2 Mouse mAb 鼠单抗进行目的蛋白检测;(图 D) 使用p44/42 MAPK (Erk1/2)Rabbit mAb 兔单抗进行目的蛋白检测。 图 7 免疫组化实验检测Akt表达 注:使用 Anti-Akt (pan) Rabbit mAb 对正常小鼠肝组织进行免疫组织化学分析。(图 E)使用免疫组化试剂盒 M&R HRP/DAB Detection IHC Kit,抗体1:100 稀释;(图F)使用另一种试剂盒,抗体 1:100 稀释。

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

      kidney D-amino-acid oxidase (Sigma, St. Louis, MO or Boehringer Mannheim, Germany) was used as a control. Organs, tissues, or tissue culture cells were homogenized in distilled water and centrifuged at 550 x g for 5 min. The supernatant solutions

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