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Anti praptor 792

Manufactured by Cell Signaling Technology
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Anti-pRaptor(792) is a primary antibody that recognizes phosphorylated Raptor at serine 792. Raptor is a regulatory subunit of the mTORC1 complex, which plays a crucial role in cell growth and metabolism regulation.

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Lab products found in correlation

Anti k48 ubiquitin, by Cell Signaling Technology (2 mentions) Mg132, by Merck Group (2 mentions) Anti sirt1, by Cell Signaling Technology (2 mentions) Srt1720, by Selleck Chemicals (2 mentions) Anti rl2, by Santa Cruz Biotechnology (2 mentions) Anti ogt, by Merck Group (2 mentions) Anti o glcnac, by Merck Group (2 mentions) Anti mmp2, by Cell Signaling Technology (2 mentions) Compound c, by Selleck Chemicals (2 mentions) Anti actin, by Santa Cruz Biotechnology (2 mentions) P erk1 2, by Merck Group (2 mentions) Integrin α5, by BD (2 mentions) Anti mmp9, by Novus Biologicals (2 mentions) Ex527, by Selleck Chemicals (2 mentions) Anti foxm1, by Santa Cruz Biotechnology (2 mentions) Anti raptor, by Cell Signaling Technology (2 mentions)

Close spelling variants of this product

Anti-pRaptor (2 citations)

2 protocols using anti praptor 792

1

Protein Modification and Regulation Assays

Cited 1 time
Check if the same lab product or an alternative is used in the 5 most similar protocols
NButGT, Ac-5SGlcNAc were provided by D. Vocadlo (Simon Fraser University)(48 (link)). SRT1720, EX-527, Compound C purchased from Selleck-Chemicals (Houston, TX). MG132 purchased from Sigma-Aldrich (St. Louis, MO). pcDNA3.1-SIRT1-Flag was gift from E. Verdin (Addgene plasmid#: 13812). pLenti4-HA-OGT (provided by K. Vosseller, Drexel University). Antibodies used: anti-actin, anti-FOXM1 and anti-RL2 from Santa Cruz Biotechnology; pERK1/2, anti-OGT and anti-O-GlcNAc from Sigma-Aldrich; anti-acetylated p53(K382), anti-AMPK, anti-pAMPK(S172), anti-ERK1/2, anti-MMP2, anti-pRaptor(792), anti-Raptor, anti-SIRT1 and anti-Ubiquitin(K48) from Cell Signaling (Danvers, MA); anti-Cdh1 and anti-p53 from Neobiolabs; anti-MMP9 from Novus-Biologicals (Littleton, CO); integrin α5 and α6 are from BD-Pharmingen (San Jose, CA).
Ferrer C.M., Lu T.Y., Bacigalupa Z.A., Katsetos C.D., Sinclair D.A, & Reginato M.J. (2016). O-GlcNAcylation regulates breast cancer metastasis via SIRT1 modulation of FOXM1 pathway. Oncogene, 36(4), 559-569.
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2

Protein Modification and Regulation Assays

Cited 1 time
Check if the same lab product or an alternative is used in the 5 most similar protocols
NButGT, Ac-5SGlcNAc were provided by D. Vocadlo (Simon Fraser University)(48 (link)). SRT1720, EX-527, Compound C purchased from Selleck-Chemicals (Houston, TX). MG132 purchased from Sigma-Aldrich (St. Louis, MO). pcDNA3.1-SIRT1-Flag was gift from E. Verdin (Addgene plasmid#: 13812). pLenti4-HA-OGT (provided by K. Vosseller, Drexel University). Antibodies used: anti-actin, anti-FOXM1 and anti-RL2 from Santa Cruz Biotechnology; pERK1/2, anti-OGT and anti-O-GlcNAc from Sigma-Aldrich; anti-acetylated p53(K382), anti-AMPK, anti-pAMPK(S172), anti-ERK1/2, anti-MMP2, anti-pRaptor(792), anti-Raptor, anti-SIRT1 and anti-Ubiquitin(K48) from Cell Signaling (Danvers, MA); anti-Cdh1 and anti-p53 from Neobiolabs; anti-MMP9 from Novus-Biologicals (Littleton, CO); integrin α5 and α6 are from BD-Pharmingen (San Jose, CA).
Ferrer C.M., Lu T.Y., Bacigalupa Z.A., Katsetos C.D., Sinclair D.A, & Reginato M.J. (2016). O-GlcNAcylation regulates breast cancer metastasis via SIRT1 modulation of FOXM1 pathway. Oncogene, 36(4), 559-569.
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