Revision 2

#13777Store at +4C

 

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Species Cross Reactivity

H

UniProt ID:

#Q13541

Entrez-Gene Id:

#1978

Cell Signaling Technology

Orders: 877-616-CELL (2355) [email protected]

Support: 877-678-TECH (8324)

Web: [email protected] cellsignal.com

3 Trask LaneDanversMassachusetts01923USA
For Research Use Only. Not for Use in Diagnostic Procedures.
Product Includes Product # Quantity Color Storage Temp
Phospho-4E-BP1 (Ser65) Rabbit Detection mAb (Biotinylated) 13814 1 ea Green (Lyophilized) +4C
HRP-Linked Streptavidin (ELISA Formulated) 11805 1 ea Red (Lyophilized) +4C
Detection Antibody Diluent 13339 11 ml Green +4C
HRP Diluent 13515 11 ml Red +4C
TMB Substrate 7004 11 ml Colorless +4C
STOP Solution 7002 11 ml Colorless +4C
ELISA Wash Buffer (20X) 9801 25 ml Colorless +4C
ELISA Sample Diluent 11083 25 ml Blue +4C
Sealing Tape 54503 2 ea +4C
Cell Lysis Buffer (10X) 9803 15 ml Yellowish -20C

*The microwell plate is supplied as 12 8-well modules - Each module is designed to break apart for 8 tests.

Description

PathScan® Phospho-4E-BP1 (Ser65) Sandwich ELISA Kit is a solid phase sandwich enzyme-linked immunosorbent assay (ELISA) that detects endogenous levels of 4E-BP1 when phosphorylated at Ser65. A total 4E-BP1 Rabbit mAb has been coated onto the microwells. After incubation with cell lysates, 4E-BP1 protein is captured by the coated antibody. Following extensive washing, a biotinylated Phospho-4E-BP1 (Ser65) Rabbit mAb Detection Antibody is added to detect the captured phospho-4E-BP1 protein. HRP-linked streptavidin is then used to recognize the bound detection antibody. HRP substrate, TMB, is added to develop color. The magnitude of absorbance for this developed color is proportional to the quantity of 4E-BP1 phosphorylated at Ser65.
Antibodies in kit are custom formulations specific to kit.

Specificity/Sensitivity

PathScan® Phospho-4E-BP1 (Ser65) Sandwich ELISA Kit detects endogenous levels of 4E-BP1 protein when phosphorylated at Ser65, as shown in Figure 1. The kit sensitivity is shown in Figure 2. This kit detects proteins from the indicated species, as determined through in-house testing, but may also detect homologous proteins from other species.

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, 762-7.
  2. Brunn, G.J. et al. (1997) Science 277, 99-101.
  3. Gingras, A.C. et al. (1998) Genes Dev 12, 502-13.
  4. Fadden, P. et al. (1997) J Biol Chem 272, 10240-7.
  5. Gingras, A.C. et al. (1999) Genes Dev 13, 1422-37.

Background References

    Cross-Reactivity Key

    H: human M: mouse R: rat Hm: hamster Mk: monkey Vir: virus Mi: mink C: chicken Dm: D. melanogaster X: Xenopus Z: zebrafish B: bovine Dg: dog Pg: pig Sc: S. cerevisiae Ce: C. elegans Hr: horse GP: Guinea Pig Rab: rabbit All: all species expected

    Trademarks and Patents

    Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc.
    PathScan is a trademark of Cell Signaling Technology, Inc.
    All other trademarks are the property of their respective owners. Visit cellsignal.com/trademarks for more information.

    Limited Uses

    Except as otherwise expressly agreed in a writing signed by a legally authorized representative of CST, the following terms apply to Products provided by CST, its affiliates or its distributors. Any Customer's terms and conditions that are in addition to, or different from, those contained herein, unless separately accepted in writing by a legally authorized representative of CST, are rejected and are of no force or effect.

    Products are labeled with For Research Use Only or a similar labeling statement and have not been approved, cleared, or licensed by the FDA or other regulatory foreign or domestic entity, for any purpose. Customer shall not use any Product for any diagnostic or therapeutic purpose, or otherwise in any manner that conflicts with its labeling statement. Products sold or licensed by CST are provided for Customer as the end-user and solely for research and development uses. Any use of Product for diagnostic, prophylactic or therapeutic purposes, or any purchase of Product for resale (alone or as a component) or other commercial purpose, requires a separate license from CST. Customer shall (a) not sell, license, loan, donate or otherwise transfer or make available any Product to any third party, whether alone or in combination with other materials, or use the Products to manufacture any commercial products, (b) not copy, modify, reverse engineer, decompile, disassemble or otherwise attempt to discover the underlying structure or technology of the Products, or use the Products for the purpose of developing any products or services that would compete with CST products or services, (c) not alter or remove from the Products any trademarks, trade names, logos, patent or copyright notices or markings, (d) use the Products solely in accordance with CST Product Terms of Sale and any applicable documentation, and (e) comply with any license, terms of service or similar agreement with respect to any third party products or services used by Customer in connection with the Products.

    Revision 2
    #13777

    PathScan® Phospho-4E-BP1 (Ser65) Sandwich ELISA Kit

    PathScan® Phospho-4E-BP1 (Ser65) Sandwich ELISA Kit: Image 1 Expand Image
    Figure 1: Treatment of HEK-293T cells with amino acids and insulin stimulates phosphorylation of 4E-BP1 at Ser65, as detected by PathScan® Phospho-4E-BP1 (Ser65) Sandwich ELISA kit #13777, but does not affect the level of total 4E-BP1 protein detected by western analysis. HEK-293T cells (70-80% confluent) were starved overnight and deprived of amino acids for 1 hr. The amino acids were replenished for 1 hr. Cells were either untreated (-) or stimulated with 100 nM insulin for 30 min at 37o C (+). Treatment of control cell lysates with λ phosphatase (4000 U/ml, 60 min, 37o C) abolishes the basal phosphorylation of 4E-BP1 as shown by both sandwich ELISA and western blot analysis. The absorbance readings at 450 nm are shown in the top figure, while the corresponding western blots, using 4E-BP1 (53H11) Rabbit mAb #9644 (left panel) or Phospho-4E-BP1 (Ser65) (174A9) Rabbit mAb #9456 (right panel), are shown in the bottom figure.
    PathScan® Phospho-4E-BP1 (Ser65) Sandwich ELISA Kit: Image 2 Expand Image
    Figure 2: The relationship between protein concentration of lysates from amino acid (AA)/untreated and AA/insulin-treated HEK-293T and the absorbance at 450 nm as detected by the PathScan® Phospho-4E-BP1 (Ser65) Sandwich ELISA Kit is shown.