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MTOR Antibody (OASG04742)

Catalog#: OASG04742
Domestic: within 1 week delivery | International: 1 week
More Information
Predicted Species ReactivityHuman, Mouse, Rat
Product FormatLiquid. PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ApplicationWB, IHC, IF
Additional InformationCellular Localization: Endoplasmic reticulum membrane Golgi apparatus membrane Mitochondrion outer membrane Lysosome Cytoplasm Nucleus, PML body Microsome membrane. Shuttles between cytoplasm and nucleus. Accumulates in the nucleus in response to hypoxia . Targeting to lysosomes depends on amino acid availability and RRAGA and RRAGB .
Tissue Specificity: Expressed in numerous tissues, with highest levels in testis.
Reconstitution and StorageStore at -20C. Avoid repeated freeze/thaw cycles.
ImmunogenSynthesized peptide derived between 2390-2470 amino acids from human mTOR around the non-phosphorylation site of S2448.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Datasheets/ManualsPrintable datasheet for anti-MTOR (OASG04742) antibody
Target Post-Translational ModificationAutophosphorylates when part of mTORC1 or mTORC2. Phosphorylation at Ser-1261, Ser-2159 and Thr-2164 promotes autophosphorylation. Phosphorylation in the kinase domain modulates the interactions of MTOR with RPTOR and PRAS40 and leads to increased intrinsic mTORC1 kinase activity. Phosphorylation at Thr-2173 in the ATP-binding region by AKT1 strongly reduces kinase activity.
SpecificitymTOR Polyclonal Antibody detects endogenous levels of mTOR protein.
Application InfoWB: 1:500-1:2000
IHC: 1:100-1:300
IF: 1:200-1:1000
ELISA: 1:40000
Optimal dilutions should be determined by the end user.
Gene SymbolMTOR
Official Gene Full Namemechanistic target of rapamycin (serine/threonine kinase)
Alias SymbolsmTOR; Serine/threonine-protein kinase mTOR; FK506-binding protein 12-rapamycin complex-associated protein 1; FKBP12-rapamycin complex-associated protein ; FRAP; RAFT1
NCBI Gene Id2475
Description of TargetSerine/threonine protein kinase which is a central regulator of cellular metabolism, growth and survival in response to hormones, growth factors, nutrients, energy and stress signals. MTOR directly or indirectly regulates the phosphorylation of at least 800 proteins. Functions as part of 2 structurally and functionally distinct signaling complexes mTORC1 and mTORC2 (mTOR complex 1 and 2). Activated mTORC1 up-regulates protein synthesis by phosphorylating key regulators of mRNA translation and ribosome synthesis. This includes phosphorylation of EIF4EBP1 and release of its inhibition toward the elongation initiation factor 4E (eiF4E). Moreover, phosphorylates and activates RPS6KB1 and RPS6KB2 that promote protein synthesis by modulating the activity of their downstream targets including ribosomal protein S6, eukaryotic translation initiation factor EIF4B, and the inhibitor of translation initiation PDCD4. Stimulates the pyrimidine biosynthesis pathway, both by acute regulation through RPS6KB1-mediated phosphorylation of the biosynthetic enzyme CAD, and delayed regulation, through transcriptional enhancement of the pentose phosphate pathway which produces 5-phosphoribosyl-1-pyrophosphate (PRPP), an allosteric activator of CAD at a later step in synthesis, this function is dependent on the mTORC1 complex. Regulates ribosome synthesis by activating RNA polymerase III-dependent transcription through phosphorylation and inhibition of MAF1 an RNA polymerase III-repressor. In parallel to protein synthesis, also regulates lipid synthesis through SREBF1/SREBP1 and LPIN1. To maintain energy homeostasis mTORC1 may also regulate mitochondrial biogenesis through regulation of PPARGC1A. mTORC1 also negatively regulates autophagy through phosphorylation of ULK1.
Swissprot IdP42345, Q9JLN9, P42346
Molecular Weight288 kDa
Tissue ToolFind tissues and cell lines supported by DNA array analysis to express MTOR.
RNA SeqFind tissues and cell lines supported by RNA-seq analysis to express MTOR.
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