Recombinant Human SLC37A4 protein (ab116881)

製品の概要

製品の詳細

  • 由来Recombinant
  • 由来Wheat germ
  • アミノ酸配列
    • アクセッション番号O43826
    • 生物種Human
    • 配列RKTFSFVMPSLVEEIPLDKDDLGFITSSQSAAYAISKFVSGVLSDQMSA
    • 分子量31 kDa including tags
    • 領域28 to 76

特性

Our Abpromise guarantee covers the use of ab116881 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

  • アプリケーション

    ELISA

    SDS-PAGE

    Western blot

  • 製品の状態Liquid
  • 備考Protein concentration is above or equal to 0.05 mg/ml.
    Best used within three months from the date of receipt.
  • Concentration information loading...

前処理および保存

  • 保存方法および安定性

    Shipped on dry ice. Upon delivery aliquot and store at -80ºC. Avoid freeze / thaw cycles.

    pH: 8.00
    Constituents: 0.3% Glutathione, 0.79% Tris HCl

関連情報

  • 別名
    • G6PT1
    • G6PT1_HUMAN
    • G6PT2
    • G6PT3
    • Glucose-5-phosphate transporter
    • Glucose-6-phosphatase, transport (glucose) protein 3
    • Glucose-6-phosphatase, transport (glucose-6-phosphate) protein 1
    • Glucose-6-phosphatase, transport (phosphate/pyrophosphate) protein 2;
    • Glucose-6-phosphate translocase
    • Glucose-6-phosphate transporter 1
    • GSD1b
    • GSD1c
    • GSD1d
    • MGC15729
    • Microsomal glucose-6-phosphate transporter
    • PRO0685
    • SLC37A4
    • Solute carrier family 37 (glucose-6-phosphate transporter), member 4
    • Solute carrier family 37 member 4
    • Transformation-related gene 19 protein
    • TRG-19
    • TRG19
    see all
  • 機能Transports glucose-6-phosphate from the cytoplasm to the lumen of the endoplasmic reticulum. Forms with glucose-6-phosphatase the complex responsible for glucose production through glycogenolysis and gluconeogenesis. Hence, it plays a central role in homeostatic regulation of blood glucose levels.
  • 組織特異性Mostly expressed in liver and kidney.
  • 関連疾患Defects in SLC37A4 are the cause of glycogen storage disease type 1B (GSD1B) [MIM:232220]. GSD1B is a metabolic disorder characterized by impairment of terminal steps of glycogenolysis and gluconeogenesis. GSD1 patients manifest a wide range of clinical symptoms and biochemical abnormalities, including hypoglycemia, severe hepatomegaly due to excessive accumulation of glycogen, kidney enlargement, growth retardation, lactic acidemia, hyperlipidemia, and hyperuricemia. GSD1B patients also present a tendency towards infections associated with neutropenia, relapsing aphthous gingivostomatitis, and inflammatory bowel disease.
    Defects in SLC37A4 are the cause of glycogen storage disease type 1C (GSD1C) [MIM:232240].
    Defects in SLC37A4 are the cause of glycogen storage disease type 1D (GSD1D) [MIM:232240].
  • 配列類似性Belongs to the major facilitator superfamily. Organophosphate:Pi antiporter (OPA) (TC 2.A.1.4) family.
  • 細胞内局在Endoplasmic reticulum membrane.
  • Information by UniProt

Recombinant Human SLC37A4 protein 画像

  • 12.5% SDS-PAGE showing ab116881 at approximately 31.02kDa stained with Coomassie Blue.

Recombinant Human SLC37A4 protein (ab116881) 使用論文

ab116881 has not yet been referenced specifically in any publications.

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