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Immunoway/Tuberin/TSC2 (phospho-Ser1254) rabbit pAb/20ug 50ug 100ug/YP1538188bio精品生物—专注于实验室精品爆款的电商平台 - 蚂蚁淘旗下精选188款生物医学科研用品
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Immunoway/Tuberin/TSC2 (phospho-Ser1254) rabbit pAb/20ug 50ug 100ug/YP1538

Tuberin/TSC2 (phospho-Ser1254) rabbit pAb

  • Catalog No.:YP1538
  • Applications:WB
  • Reactivity:Human,Mouse,Rat
  • Data Sheet
  • MSDS
  • Support
  • Description
  • References ( 0 )
  • Protocol
    • Gene Name:
    • TSC2 TSC4
    • Protein Name:
    • Tuberin/TSC2 (Ser1254)
    • Human Gene Id:
    • 7249
    • Human Swiss Prot No:
    • P49815
    • Mouse Swiss Prot No:
    • Q61037
    • Rat Gene Id:
    • 24855
    • Rat Swiss Prot No:
    • P49816
    • Immunogen:
    • Synthesized phosho peptide around human Tuberin(Ser1254)
    • Specificity:
    • This antibody detects endogenous levels ofHuman Mouse Rat Tuberin/TSC2 (phospho-Ser1254)
    • Formulation:
    • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
    • Source:
    • Rabbit
    • Dilution:
    • WB 1:1000-2000
    • Purification:
    • The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
    • Concentration:
    • 1 mg/ml
    • Storage Stability:
    • -20°C/1 year
    • Other Name:
    • Tuberin (Tuberous sclerosis 2 protein)
    • Observed Band(KD):
    • 200
    • Background:
    • tuberous sclerosis 2(TSC2)Homo sapiensMutations in this gene lead to tuberous sclerosis complex. Its gene product is believed to be a tumor suppressor and is able to stimulate specific GTPases. The protein associates with hamartin in a cytosolic complex, possibly acting as a chaperone for hamartin. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008],
    • Function:
    • alternative products:Additional isoforms seem to exist. Experimental confirmation may be lacking for some isoforms,disease:Defects in TSC2 are a cause of lymphangioleiomyomatosis (LAM) [MIM:606690]. LAM is a progressive and often fatal lung disease characterized by a diffuse proliferation of abnormal smooth muscle cells in the lungs. It affects almost exclusively young women and can occur as an isolated disorder or in association with tuberous sclerosis complex.,disease:Defects in TSC2 are the cause of tuberous sclerosis complex (TSC) [MIM:191100]. The molecular basis of TSC is a functional impairment of the tuberin-hamartin complex. TSC is an autosomal dominant multi-system disorder that affects especially the brain, kidneys, heart, and skin. TSC is characterized by hamartomas (benign overgrowths predominantly of a cell or tissue type that occurs normally in the organ) and hamartias (de
    • Subcellular Location:
    • nucleus,cytoplasm,lysosome,Golgi apparatus,cytosol,membrane,TSC1-TSC2 complex,perinuclear region of cytoplasm,
    • Expression:
    • Blood,Brain,Endometrium,Epithelium,Lymph,Lymphoblast,Peripheral blood leukocyte,Pla
    • June 19-2018
    • WESTERN IMMUNOBLOTTING PROTOCOL
    • June 19-2018
    • IMMUNOHISTOCHEMISTRY-PARAFFIN PROTOCOL
    • June 19-2018
    • IMMUNOFLUORESCENCE PROTOCOL
    • June 19-2018
    • FLOW CYTOMEYRT PROTOCOL
    • July 13-2018
    • CELL-BASED-ELISA-PROTOCOL-FOR-ACETYL-PROTEIN
    • July 13-2018
    • CELL-BASED-ELISA-PROTOCOL-FOR-PHOSPHO-PROTEIN
    • July 13-2018
    • CELL-BASED-COLORIMETRIC-ELISA-PROTOCOL-FOR-TOTAL-PROTEIN
    • July 13-2018
    • Antibody-FAQs
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