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OriGene Antibodies in recent publications
A common polymorphism in the LDL receptor gene has multiple effects on LDL receptor function Hum. Mol. Genet., Apr 2013; 22: 1424 - 1431. [anti-DDK]

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Modulation of TET2 expression and 5-methylcytosine oxidation by the CXXC domain protein IDAX Nature 497, 122-126 doi:10.1038/nature12052 [anti-DDK]

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Home All anti-TSC2 antibodies

Anti-TSC2 Phospho Antibody EPR1060(2)

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Specifications Related Products Conjugation/Bulk FAQs
SKU Description Amount Price Availability*  
TA307814
  • Rabbit monoclonal antibody against TSC2 / Tuberin Phospho (pT1462)(clone EPR1060(2)) (Phospho-Specific)
100ul $325 3-7 Days Add to Shopping Cart
WB(1)
IHC(1)
Gene NameHomo sapiens tuberous sclerosis 2 (TSC2), transcript variant 1
Synonyms:LAM; TSC4
ImmunogenA phospho specific peptide corresponding to residues surrounding Threonine 1462 of human TSC2/Tuberin was used as an immunogen. This antibody only detects TSC2/Tuberin phosphorylated at Threonine 1462.
BufferStore at -20 C. Buffer: 50 mM Tris-Glycine (pH 7.4), 0.15 M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% BSA. Stable for 12 months from date of receipt.
Clone NameEPR1060(2) IsotypeRabbit IgG
Species ReactivityHuman, Mouse Concentration
Guaranteed Application *WB, IHC Suggested DilutionsICC: 1:100-250, IHC: 1:50-100, WB: 1:1,000-10,000,
BackgroundTuberous sclerosis complex-2 (TSC2 also known as Tuberin) is a tumor suppressor that forms a complex with TSC1 (Hamartin ) and this complex is known to control various cellular functions including cell cycle, endocytosis, adhesion, and transcription (1). The C-terminal region of TSC2 contains a GTPase-activating protein (GAP) domain which interacts with Rap1, Rab5 and Rheb (2). The TSC1/TSC2 complex inhibits phosphorylation of S6kinase and 4E-BP1 through inactivation of mTOR (3). Tuberin is a target for phosphorylation by several kinases including Akt, which directly phosphorylates and inactivates TSC2 on Ser 924, Thr 1462 and Thr 1518. These phosphorylations by Akt disrupt the TSC1-TSC2 complex and disturb the subcellular localization of TSC1 and TSC2. Tuberous sclerosis (TSC), an autosomal dominant disorder that affects 1 in 6000 newborns, is caused by a mutation in either the TSC1 or TSC2 tumor suppressor gene (4).
Related Pathway

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WB Image
Western blot analysis on NIH/3T3 cell lysates using anti-Phospho-TSC2/Tuberin (pT1462) RabMAb .
IHC Image
Immunohistochemical analysis of paraffin-embedded human liver tissue using anti-Phospho TSC2/Tuberin (pT1462) RabMAb .

 

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