Purified anti-TSC2 Antibody anti-TSC2 - W16104A,BioLegend,697701

This clone does not work for IF application (in house tested).Antibody specificity was confirmed by knock-down of TSC2 using siRNA (in-house tested).

Host

Rat

Reactivity

Human, Mouse

Application

WB -Quality testedKO/KD-WB -Verified

Platform ID

BAB703841518

BioLegend

Headquarters

8999 BioLegend Way San Diego, CA 92121 United States

Contact

Tel: 1-858-455-9588
Fax: +49 (4131) 7023913

Email:

Product Specifications
Scientific Background

Specifications

NamePurified anti-TSC2 Antibody anti-TSC2 - W16104A
Cat. No.697701
HostRat
RRIDAB_2687204 (BioLegend Cat. No. 697701)AB_2687188 (BioLegend Cat. No. 697702)
IsotypeRat IgG2a, κ
ReactivityHuman, Mouse
ApplicationWB -Quality testedKO/KD-WB -Verified
ClonalityMonoclonal
Clone NumberW16104A
Concentration0.5 mg/ml
TargetTSC2
ImmunogenHuman TSC2 recombinant protein (1508-1807 amino acid) expressed inE. coli.
PurityThe antibody was purified by affinity chromatography.
FormulationPhosphate-buffered solution, pH 7.2, containing 0.09% sodium azide.
StorageThe antibody solution should be stored undiluted between 2°C and 8°C.
Regulatory StatusResearch Use Only

Scientific Background

Tuberous sclerosis 2 (TSC2) forms the tuberous sclerosis complex with TSC1 and functions as a crucial negative regulator of the Rheb/mTOR pathway. mTOR belongs to the PI3K-related kinase family and regulates protein translation, cell proliferation, and cell differentiation. Activation of mTOR requires binding to the active small GTPase Ras homolog enriched in brain (Rheb). TSC2 acts as a GTPase activating protein (GAP) and inhibits mTORC1 through converting active GTP-bound Rheb to inactive GDP-bound Rheb. Phosphorylation of TSC2 by AKT leads to inactivation of the tuberous sclerosis complex and in turn results in the activation of the Rheb/mTOR pathway. Mutations in the TSC2 gene lead to hyperactivation of the Rheb/mTOR pathway and are associated with the autosomal dominant disorder tuberous sclerosis and pulmonary lymphangioleiomyomatosis (LAM).

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