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Each lot of this antibody is quality control tested by immunofluorescence staining. For immunofluorescence microscopy: Use a dilution range of 1:100~1:400. It is recommended that the reagent be titrated. For IHC, use a 1:50 dilution of antibody for staining. Antigen retrieval for IHC of formalin-fixed paraffin-embedded tissue using 0.01 M sodium citrate buffer is recommended.
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Application Notes:
The Poly6359 antibody recognizes human phospho-TSC2 (Ser664) and has been shown to be useful for immunofluorescent staining. This antibody does not detect TSC2 phosphorylated at other sites.
Application References:
1. Bartolome A, et al. 2010. Endocrinology. PubMed 2. Miyazaki M, et al. 2011. J Physiol. 589:1831. PubMed.
Untreated Hela cells (Panel A), or overnight nocodazole treated Hela cells (Panel B) stained with purified rabbit polyclonal antibody Poly6359 against phospho-TSC2 (Ser664), followed by Cy3-conjugated Donkey anti-rabbit IgG and DAPI.
Formalin-fixed paraffin-embedded human epidermis tissue was stained with Poly6359 and developed with an alkaline phosphatase chromogen substate (red color). Tissue was counterstained with H&E (blue/pink). Magnification, 40X.
Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder that is caused by mutation in either the TSC1 (hamartin) or TSC2 (tuberin) gene. TSC1 and TSC2 proteins form a physical and functional heterodimer in vivo thatinhibits ribosomal protein S6 kinase 1 (S6K1) and activates eukaryotic initiation factor 4E-bindingprotein 1 (4E-BP1) by inhibition of the mammalian target of rapamycin (mTOR). TSC2 belongs to small GTPase protein of the Ras superfamily, contain a Rap-GAP domain. Predicted molecular weight 201 kD. Ser664 TSC2 phosphorylation leads to TSC1-TSC2 dissociation and markedly impairs TSC2 ability to inhibit mTOR signaling, cell proliferation, and oncogenic transformation. Erk (extracellular signal-regulated kinase) may contribute to tumorigenesis by phosphorylating TSC2 at specific residues, particularly S664.
Other Names:
Tuberin, Tuberous sclerosis 2 protein, TSC4
Structure:
Belongs to small GTPase protein of the Ras superfamily, contain a Rap-GAP domain. TSC2 has an NH2-terminal leucine zipper necessary for TSC1 binding and a COOH-terminal domain similar to that found in GTPase-activating proteins. Predicted molecular weight
Distribution:
Cytoplasm protein and is expressed in liver, brain, heart, lymphocytes, fibroblasts, biliary epithelium, pancreas, skeletal muscle, kidney, lung and placenta.
Function:
Negatively regulates cell growth and proliferation as a TSC1-TSC2 heterodimer. TCS2 is believed to be a tumor suppressor and is able to stimulate specific GTPases.
Interaction:
14-3-3, AKT1, AKT3, ERK2, TSC1, Protein kinase B beta, Estrogen receptor alpha, SMAD3, p27Kip1, RAB5
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This data display is provided for general comparisons between formats. Your actual data may vary due to variations in samples, target cells, instruments and their settings, staining conditions, and other factors. If you need assistance with selecting the best format contact our expert technical support team.
Purified anti-TSC2 Phospho (Ser664)
Untreated Hela cells (Panel A), or overnight nocodazole treated Hela cells (Panel B) stained with purified rabbit polyclonal antibody Poly6359 against phospho-TSC2 (Ser664), followed by Cy3-conjugated Donkey anti-rabbit IgG and DAPI.
Formalin-fixed paraffin-embedded human epidermis tissue was stained with Poly6359 and developed with an alkaline phosphatase chromogen substate (red color). Tissue was counterstained with H&E (blue/pink). Magnification, 40X.