This antibody is purified through a protein A column, followed by peptide affinity purification.
Immunogène
This TSC2 Antibody is generated from rabbits immunized with a KLH conjugated synthetic phosphopeptide corresponding to amino acid residues surrounding S1387 of human TSC2.
TSC2
Reactivité: Humain
DB
Hôte: Lapin
Polyclonal
RB13340
unconjugated
Indications d'application
IF: 1:10~50. DB: 1:500
Restrictions
For Research Use only
Format
Liquid
Buffer
Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
Agent conservateur
Sodium azide
Précaution d'utilisation
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Stock
4 °C,-20 °C
Date de péremption
6 months
Huang, Ratovitski: "Phospho-?Np63?/Rpn13-dependent regulation of LKB1 degradation modulates autophagy in cancer cells." dans: Aging, Vol. 2, Issue 12, pp. 959-68, (2011) (PubMed).
Li, Inoki, Guan: "Biochemical and functional characterizations of small GTPase Rheb and TSC2 GAP activity." dans: Molecular and cellular biology, Vol. 24, Issue 18, pp. 7965-75, (2004) (PubMed).
Karbowniczek, Cash, Cheung, Robertson, Astrinidis, Henske: "Regulation of B-Raf kinase activity by tuberin and Rheb is mammalian target of rapamycin (mTOR)-independent." dans: The Journal of biological chemistry, Vol. 279, Issue 29, pp. 29930-7, (2004) (PubMed).
Corradetti, Inoki, Bardeesy, DePinho, Guan: "Regulation of the TSC pathway by LKB1: evidence of a molecular link between tuberous sclerosis complex and Peutz-Jeghers syndrome." dans: Genes & development, Vol. 18, Issue 13, pp. 1533-8, (2004) (PubMed).
Birchenall-Roberts, Fu, Bang, Dambach, Resau, Sadowski, Bertolette, Lee, Kim, Ruscetti: "Tuberous sclerosis complex 2 gene product interacts with human SMAD proteins. A molecular link of two tumor suppressor pathways." dans: The Journal of biological chemistry, Vol. 279, Issue 24, pp. 25605-13, (2004) (PubMed).
Lewis, Thomas, Murphy, Sampson: "Genotype and psychological phenotype in tuberous sclerosis." dans: Journal of medical genetics, Vol. 41, Issue 3, pp. 203-7, (2004) (PubMed).
Mutations in TSC2 lead to tuberous sclerosis complex. The protein is believed to be a tumor suppressor and is able to specifically stimulate the intrinsic GTPase activity of the Ras-related protein RAP1A and RAB5. The protein associates with hamartin in a cytosolic complex, possibly acting as a chaperone for hamartin. TSC2 may have a function in vesicular transport, but may also play a role in the regulation of cell growth arrest and in the regulation of transcription mediated by steroid receptors. Interaction between TSC1 and TSC2 may facilitate vesicular docking.