pmtor ser2448 (Cell Signaling Technology Inc)
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Cell Signaling Technology Inc
pmtor ser2448
Pmtor Ser2448, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 3437 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/pmtor+ser2448/Phospho-mTOR+(Ser2448)+XP+Rabbit+mAb/pmc13049662-40-1-4
Average 97 stars, based on 3437 article reviews
Pmtor Ser2448, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 3437 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/pmtor+ser2448/Phospho-mTOR+(Ser2448)+XP+Rabbit+mAb/pmc13049662-40-1-4
Average 97 stars, based on 3437 article reviews
pmtor ser2448 - by Bioz Stars,
2026-09
97/100 stars
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Western Blot:Article Title: Uncoupling of Akt and mTOR signaling drives resistance to Akt inhibition in PTEN loss prostate cancers. Article Snippet: .. The following antibodies were used for Western blotting: PSA (5365S), pAkt (Ser473) (Cell Signaling Technology, 4060L), pAkt (Thr308) (Cell Signaling Technology, 4056S), pEGFR (Cell Signaling Technology, 3777S), p- p44/42 MAPK (Erk1/2) (Thr202/Tyr204) (D13.14.4E) XP (Cell Signaling Technology, 4370S), pMEK1/2 (Ser217/221) (41G9) (Cell Signaling Technology, 9154S), pS6K (Thr389) (Cell Signaling Technology, 9205L), pS6 (Ser235/236) (Cell Signaling Technology, 4856S), PTEN (Cell Signaling Technology, 9188L), pPRAS40 (Thr246) (Cell Signaling Technology, 2997S), p4EBP1 (Thr37/46) (Cell Signaling Technology, 2855L), other:Article Title: AMPK inhibition and elevated angiogenin are associated with tRNA fragmentation in the male germline exposed to a high-fat diet Article Snippet: , Incubation:Article Title: Liver impact of growth hormone (GH) intermittent treatment during the growth period in mice. Article Snippet: Liver impact of prolonged GH-treatment given to non-GH-deficient growing mice between the third and eighth week of life was evaluated in both sexes.. Tissues were collected 6 h after last dose or four weeks later.. Somatometric, biochemical, histological, immunohistochemical, RT-qPCR and immunoblotting determinations were Article Title: A modular microfluidic platform to study how fluid shear stress alters estrogen receptor phenotype in ER+ breast cancer cells Article Snippet: The blots were blocked by incubation in EveryBlot blocking buffer (BIO-RAD 12010020) per manufacturer’s protocol. .. After blocking, the membrane was incubated with primary antibody overnight at 4°C for p-AKT (Ser473) (Cell Signaling Technologies, #4060), p-ERα (Ser167) (Cell Signaling Technologies, #64508), Ubiquitin Proteomics:Article Title: GL261 glioblastoma induces delayed body weight gain and stunted skeletal muscle growth in young mice Article Snippet: Optical density measurements were taken using the ImageJ Analyzer software. .. Antibodies used were pSTAT1 (#9167), STAT1 (#9712), pSTAT3 Y705 (#9145), STAT3 (#8768), pAkt S473 (#4060), Akt (#9272), pP38 MAPK (T180/Y182) (#4511), P38 MAPK (#9212), pERK1/2 (#4370), ERK1/2 (#4695), p4EBP1 (#2855), 4EBP1 (#9644), VDAC (#4866), pFoxO3a Ser253 (#9466), FoxO3a (#12829), OPA1 (#80471), Article Title: Targeting the IRS1 macromolecular signaling node by Trienomycin a triggers cytoprotective autophagy in pancreatic adenocarcinoma. Article Snippet: After blocking with Trisbuffered saline with 0.05 % Tween-20 (TBST) supplemented with 5 % non-fat dry milk, the NC membranes were incubated with specific primary antibodies and secondary antibody (Cell Signaling Technology) sequentially, then the membranes were visualized by using ECL solution and scanned by using the Imaging System (Alliance Q9 Advanced, Uvitec, England). .. Primary antibodies used in the paper included Pyrolysis Gas Chromatography:Article Title: GL261 glioblastoma induces delayed body weight gain and stunted skeletal muscle growth in young mice Article Snippet: Optical density measurements were taken using the ImageJ Analyzer software. .. Antibodies used were pSTAT1 (#9167), STAT1 (#9712), pSTAT3 Y705 (#9145), STAT3 (#8768), pAkt S473 (#4060), Akt (#9272), pP38 MAPK (T180/Y182) (#4511), P38 MAPK (#9212), pERK1/2 (#4370), ERK1/2 (#4695), p4EBP1 (#2855), 4EBP1 (#9644), VDAC (#4866), pFoxO3a Ser253 (#9466), FoxO3a (#12829), OPA1 (#80471), Blocking Assay:Article Title: A modular microfluidic platform to study how fluid shear stress alters estrogen receptor phenotype in ER+ breast cancer cells Article Snippet: The blots were blocked by incubation in EveryBlot blocking buffer (BIO-RAD 12010020) per manufacturer’s protocol. .. After blocking, the membrane was incubated with primary antibody overnight at 4°C for p-AKT (Ser473) (Cell Signaling Technologies, #4060), p-ERα (Ser167) (Cell Signaling Technologies, #64508), Membrane:Article Title: A modular microfluidic platform to study how fluid shear stress alters estrogen receptor phenotype in ER+ breast cancer cells Article Snippet: The blots were blocked by incubation in EveryBlot blocking buffer (BIO-RAD 12010020) per manufacturer’s protocol. .. After blocking, the membrane was incubated with primary antibody overnight at 4°C for p-AKT (Ser473) (Cell Signaling Technologies, #4060), p-ERα (Ser167) (Cell Signaling Technologies, #64508), |