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Phospho-4E-BP1 (Thr37/46) (236

B4) Rabbit mAb
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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年10月01日
  • western blot,免疫组化(IHC),免疫荧光(IF),流式细胞(Flow Cyt)
  • 人,小鼠,大鼠,驴,其他
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      Phospho-4E-BP1 (Thr37/46) (236B4) Rabbit mAb

    • 抗原

      /

    • 应用范围

      western blot,免疫组化(IHC),免疫荧光(IF),流式细胞(Flow Cyt)

    • 宿主

    • 级别

      详见MSDS文件

    • 抗原来源

      /

    • 保质期

      详见说明书

    • 库存

      大量

    • 供应商

      CST

    • 适应物种

      人,小鼠,大鼠,驴,其他

    • 是否单克隆

      1

    • 保存条件

      -20°c

    • 规格

      40 ul (4 western blots)/100 ul (10 western blots)/300 ul (30 western blots)/<a href="http://www.cellsignal.com/ddt/custom_reagents.html" target="_blank">carrier free &amp; custom formulation / quantity</a>

    规格:产品价格:¥请询价
    规格:40 ul (4 western blots)产品价格:¥请询价
    规格:100 ul (10 western blots)产品价格:¥请询价
    规格:300 ul (30 western blots)产品价格:¥请询价
    规格:<a href="http://www.cellsignal.com/ddt/custom_reagents.html" target="_blank">carrier free &amp; custom formulation / quantity</a> 产品价格:¥请询价

    Product Pathways - Translational Control

    Phospho-4E-BP1 (Thr37/46) (236B4) Rabbit mAb #2855

    Applications Reactivity Sensitivity MW (kDa) Isotype
    W IHC-P IF-IC F H M R Mk Dm Endogenous 15 to 20 Rabbit IgG

    Applications Key:  W=Western Blotting  IHC-P=Immunohistochemistry (Paraffin)  IF-IC=Immunofluorescence (Immunocytochemistry)  F=Flow Cytometry
    Reactivity Key:  H=Human  M=Mouse  R=Rat  Mk=Monkey  Dm=D. melanogaster
    Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

    Protocols

    Specificity / Sensitivity

    Phospho-4E-BP1 (Thr37/46) (236B4) Rabbit mAb detects endogenous levels of 4E-BP1 only when phosphorylated at Thr37 and/or Thr46. This antibody may cross-react with 4E-BP2 and 4E-BP3 when phosphorylated at equivalent sites.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding Thr37 and Thr46 of mouse 4E-BP1.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from 293T cells using 4E-BP1 Antibody #9452 (upper) and Phospho-4E-BP1 (Thr37/46) Antibody #2855 (lower). The cells were starved for 24 hours in serum-free medium and underwent a 1 hour amino acid deprivation. Amino acids were replenished for 1 hour. Cells were then either untreated (-) or treated with 100 nM insulin (+) for 30 minutes.

    IHC-P (paraffin)

    IHC-P (paraffin)

    Immunohistochemical analysis of paraffin-embedded human colon carcinoma using Phospho-4E-BP1 (Thr37/46) (236B4) Rabbit mAb.

    IHC-P (paraffin)

    IHC-P (paraffin)

    Immunohistochemical analysis of paraffin-embedded human lymphoma using Phospho-4E-BP1 (Thr37/46) (236B4) Rabbit mAb.


    IHC-P (paraffin)

    IHC-P (paraffin)

    Immunohistochemical analysis using Phospho-4E-BP1 (Thr37/46) (236B4) Rabbit mAb on SignalSlide (TM) Phospho-Akt (Ser473) IHC Controls #8101 (paraffin-embedded LNCaP cells untreated (left) or LY294002-treated (right)).

    IHC-P (paraffin)

    IHC-P (paraffin)

    Immunohistochemical analysis of paraffin-embedded human colon carcinoma using Phospho-4E-BP1 (Thr37/46) (236B4) Rabbit mAb in the presence of control peptide (left) or Phospho-4E-BP1 (Thr37/46) Blocking Peptide #1052 (right).

    Flow Cytometry

    Flow Cytometry

    Flow cytometric analysis of Jurkat cells, untreated (green) or LY294002, Wortmannin and U0126-treated (blue), using Phospho-4E-BP1 (Thr36/46) (236B4) Rabbit mAb compared to a nonspecific negative control antibody (red).


    IF-IC

    IF-IC

    Confocal immunofluorescent analysis of HeLa cells treated with LY294002 (left) or 20% serum (right) and labeled with Phospho-4E-BP1 (Thr37/46) (236B4) Rabbit mAb (green). Actin filaments have been labeled with Alexa Fluor® 555 phalloidin (red).

    Background

    Translation repressor protein 4E-BP1 (also known as PHAS-1) inhibits cap-dependent translation by binding to the translation initiation factor eIF4E. Hyperphosphorylation of 4E-BP1 disrupts this interaction and results in activation of cap-dependent translation (1). Both the PI3 kinase/Akt pathway and FRAP/mTOR kinase regulate 4E-BP1 activity (2,3). Multiple 4E-BP1 residues are phosphorylated in vivo (4). While phosphorylation by FRAP/mTOR at Thr37 and Thr46 does not prevent the binding of 4E-BP1 to eIF4E, it is thought to prime 4E-BP1 for subsequent phosphorylation at Ser65 and Thr70 (5).

    1. Pause, A. et al. (1994) Nature 371, 762-767.
    2. Brunn, G.J. et al. (1997) Science 277, 99-101.
    3. Gingras, A.C. et al. (1998) Genes Dev. 12, 502-513.
    4. Fadden, P. et al. (1997) J. Biol. Chem. 272, 10240-10247.
    5. Gingras, A.C. et al. (1999) Genes Dev. 13, 1422-1437.

    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

    Rabbit monoclonal antibody is produced under license (granting certain rights including those under U. S. Patent No. 5,675,063 and U.S.S.N. 11/476,277) from Epitomics, Inc.


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

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    图标文献和实验
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    • 组化染色背景高?没信号?一篇文章带你快速掌握免疫组化!

      :使用 Anti-phospho-Akt (Ser473) Rabbit mAb 对石蜡包埋的人乳腺癌组织进行免疫组织化学分析。(图 A)使用免疫组化试剂盒M&R HRP/DAB Detection IHC Kit,抗体 1:100 稀释;(图 B) 采用普通免疫组化试剂盒,抗体 1:25 稀释。 图 6 免疫组化实验检测 Erk1/2 表达 注:使用 Anti-Erk1/2 Mouse mAb与p44/42 MAPK (Erk1/2)Rabbit mAb 对正常小鼠心脏组织进行免疫

    • Studies of the Ubiquitin Proteasome System

      Assays of E1 and E2 Activity Basic Protocol 1: Thiolester Formation Between Rabbit E1 and Ubiquitin Basic Protocol 2: Thiolester Formation Between E2 and Ubiquitin Binding of Ubiquitin‐Proteasome Proteins Basic Protocol 3: Binding of E2s to E3s Alternate

    • v468. chapter 4 WNT 细胞通路 检测细胞GSK3活性与表达水平

      the range ofduplicate experiments. B Same as ( A ), except membranes were probed with antibodies that recognise phosphorylatedb-catenin (Thr41/Ser37/Ser33), total b-catenin, phosphorylated CRMP2 (Thr514/509), or total CRMP2. n.s. , non-significant;* p

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