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  • 159-2642-3062 027-65317797
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    • 產(chǎn)品名稱: Recombinant Human SLC2A1 protein
    • 產(chǎn)品貨號(hào): CSP00603
    • 貨期: 現(xiàn)貨
    • 價(jià)格與訂購(gòu): 1800
    • 數(shù)量:
      庫(kù)存: 100
    • 規(guī)格: 50μg 100μg 1mg
    • 產(chǎn)品信息
    • 如何訂購(gòu)
      概述(Summary)
      英文全稱
      Recombinant Human SLC2A1 protein
      純度(Purity)
      >90% as determined by SDS-PAGE
      內(nèi)毒素(Endotoxin level)
      Please contact with the lab for this information.
      蛋白構(gòu)建(Construction)
      A DNA sequence encoding the human SLC2A1 (Met251-Glu329) was fused with His tag
      Accession #
      P11166
      表達(dá)宿主(Host)
      E.coli
      種屬(Species)
      Homo sapiens (Human)
      預(yù)測(cè)分子量(Predicted Molecular Mass)
      10.15 kDa
      制劑(Formulation)
      Supplied as solution form in PBS pH 7.5 or lyophilized from PBS pH 7.5.
      運(yùn)輸方式(Shipping)
      In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.
      穩(wěn)定性&儲(chǔ)存(Stability &Storage)
      Use a manual defrost freezer and avoid repeated freeze thaw cycles.
      Store at 2 to 8 °C for one week .
      Store at -20 to -80 °C for twelve months from the date of receipt.
      復(fù)溶(Reconstitution)
      Reconstitute in sterile water for a stock solution.A copy of datasheet will be provided with the products, please refer to it for details.
      背景(Background)
      背景介紹
      Arterial tortuosity syndrome (ATS) is an autosomal recessive connective tissue disorder, mainly characterized by tortuosity and elongation of the large- and medium-sized arteries with predisposition to stenoses and aneurysms. ATS is caused by mutations in the SLC2A1 gene, encoding for the facilitative glucose transporter 1 (GLUT1) and is described typically in pediatric patients. The loss-of-function mutation in the gene encoding the facilitative glucose transporter GLUT1 (SLC2A1) causes arterial tortuosity syndrome via upregulation of the TGF-beta pathway in the arterial wall, a mechanism possibly causing vascular changes in diabetes. The SLC2A1 gene is an independent risk factor for PAD in type 2 diabetes.
      分子別名(Alternative Names)
      Solute carrier family 2, facilitated glucose transporter member 1,Glucose transporter type 1, erythrocyte/brain,GLUT-1,HepG2 glucose transporter.
      Note
      For research use only .
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