Product Pathways - PI3K / Akt Signaling
FoxO1 (D8T1S) Mouse mAb #97635
|97635S||100 µl ( 10 western blots )||￥3,250.00||现货查询 购买询价 防伪查询|
|97635||carrier free & custom formulation / quantity||email request|
|W||1:1000||Human,Mouse,Rat,Monkey,||Endogenous||78 to 82||Mouse IgG1|
Species cross-reactivity is determined by western blot.
Applications Key: W=Western Blotting, IP=Immunoprecipitation, IHC-P=Immunohistochemistry (Paraffin),
Specificity / Sensitivity
FoxO1 (D8T1S) Mouse mAb recognizes endogenous levels of total FoxO1 protein. The antibody does not detect exogenously expressed family members FoxO3a or FoxO4.
Source / Purification
Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Pro360 of human FoxO1 protein.
Immunohistochemical analysis of paraffin-embedded human ovarian carcinosarcoma using FoxO1 (D8T1S) Mouse mAb in the presence of control peptide (left) or antigen-specific peptide (right).
Immunohistochemical analysis of paraffin-embedded IGROV-1 cell pellets, LY294002-treated (left) or IGF-1-treated (right), using FoxO1 (D8T1S) Mouse mAb.
Western blot analysis of extracts from 293T, IGROV-1, and COS-7 cells using FoxO1 (D8T1S) Mouse mAb.
Immunohistochemical analysis of paraffin-embedded human ductal carcinoma of the breast using FoxO1 (D8T1S) Mouse mAb.
Immunohistochemical analysis of paraffin-embedded human colon carcinoma using FoxO1 (D8T1S) Mouse mAb.
The Forkhead family of transcription factors is involved in tumorigenesis of rhabdomyosarcoma and acute leukemias (1-3). Within the family, three members (FoxO1, FoxO4, and FoxO3a) have sequence similarity to the nematode orthologue DAF-16, which mediates signaling via a pathway involving IGFR1, PI3K, and Akt (4-6). Active forkhead members act as tumor suppressors by promoting cell cycle arrest and apoptosis. Increased expression of any FoxO member results in the activation of the cell cycle inhibitor p27 Kip1. Forkhead transcription factors also play a part in TGF-β-mediated upregulation of p21 Cip1, a process negatively regulated through PI3K (7). Increased proliferation results when forkhead transcription factors are inactivated through phosphorylation by Akt at Thr24, Ser256, and Ser319, which results in nuclear export and inhibition of transcription factor activity (8). Forkhead transcription factors can also be inhibited by the deacetylase sirtuin (SirT1) (9).
- Anderson, M.J. et al. (1998) Genomics 47, 187-99.
- Galili, N. et al. (1993) Nat Genet 5, 230-5.
- Borkhardt, A. et al. (1997) Oncogene 14, 195-202.
- Nakae, J. et al. (1999) J Biol Chem 274, 15982-5.
- Rena, G. et al. (1999) J Biol Chem 274, 17179-83.
- Guo, S. et al. (1999) J Biol Chem 274, 17184-92.
- Seoane, J. et al. (2004) Cell 117, 211-23.
- Arden, K.C. (2004) Mol Cell 14, 416-8.
- Yang, Y. et al. (2005) EMBO J 24, 1021-32.
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For Research Use Only. Not For Use In Diagnostic Procedures.
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Cell Signaling Technology® is a trademark of Cell Signaling Technology, Inc.
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