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Product Name
Tuberin-Specific antibody
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Description
Tuberin-Specific Rabbit Polyclonal antibody. Positive IHC detected in human kidney tissue. Positive IF detected in Hela cells. Positive WB detected in mouse lung tissue, mouse liver tissue, mouse skeletal muscle tissue, NIH/3T3 cells. Observed molecular weight by Western-blot: 170-180 kDa
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Tested applications
ELISA, WB, IF, IHC
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Species reactivity
Human,Mouse,Rat; other species not tested.
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Alternative names
FLJ43106 antibody; LAM antibody; TSC2 antibody; TSC4 antibody; Tuberin antibody; tuberous sclerosis 2 antibody; Tuberous sclerosis 2 protein antibody
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Isotype
Rabbit IgG
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Preparation
This antibody was obtained by immunization of Peptide (Accession Number: NM_000548). Purification method: Antigen affinity purified.
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Clonality
Polyclonal
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Formulation
PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
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Storage instructions
Store at -20℃. DO NOT ALIQUOT
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Applications
Recommended Dilution:
WB: 1:200-1:2000
IHC: 1:20-1:200
IF: 1:10-1:100
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Validations
mouse lung tissue were subjected to SDS PAGE followed by western blot with Catalog No:116485(TSC2-Specific antibody) at dilution of 1:300
Immunohistochemistry of paraffin-embedded human kidney slide using Catalog No:116485(TSC2-Specific Antibody) at dilution of 1:50
Immunohistochemistry of paraffin-embedded human kidney slide using Catalog No:116485(TSC2-Specific Antibody) at dilution of 1:50
Immunofluorescent analysis of Hela cells, using TSC2 antibody Catalog No:116485 at 1:25 dilution and Rhodamine-labeled goat anti-rabbit IgG (red).
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Background
TSC2, also named as TSC4, FLJ43106 and LAM, acts as a GTPase-activating protein (GAP) for the small GTPase RHEB, a direct activator of the protein kinase activity of mTORC1. In complex with TSC1, TSC2 inhibits the nutrient-mediated or growth factor-stimulated phosphorylation of S6K1 and EIF4EBP1 by negatively regulating mTORC1 signaling. TSC2 implicated as a tumor suppressor. It is involved in microtubule-mediated protein transport, but this seems to be due to unregulated mTOR signaling. TSC2 stimulates weakly the intrinsic GTPase activity of the Ras-related proteins RAP1A and RAB5 in vitro. Mutations in TSC2 lead to constitutive activation of RAP1A in tumors. Mutations in either TSC2 or the related TSC1 (hamartin) gene cause tuberous sclerosis complex (TSC), an autosomal dominant disorder characterized by development of multiple, widespread non-malignant tumors. The antibody is specific to TSC2.
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