Recombinant Human HSD11B2 protein (ab114569)

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
    • 生物種
      Human
    • 配列
      RLARPQRLPVATRAVLITGCDSGFGKETAKKLDSMGFTVLATVLELNSPG AIELRTCCSPRLRLLQMDLTKPGDISRVLEFTKAHTTSTGLWGLVNNAGH
    • 分子量
      37 kDa
    • 領域
      71 to 170

特性

Our Abpromise guarantee covers the use of ab114569 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

    SDS-PAGE

    Western blot

    ELISA

  • 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
    • 11 beta HSD2
    • 11 beta hydroxysteroid dehydrogenase type 2
    • 11 DH2
    • 11-beta-HSD2
    • 11-beta-hydroxysteroid dehydrogenase type 2
    • 11-DH2
    • AME
    • AME1
    • Corticosteroid 11 beta dehydrogenase isozyme 2
    • Corticosteroid 11-beta-dehydrogenase isozyme 2
    • DHI2_HUMAN
    • HSD11B2
    • HSD11K
    • HSD2
    • Hydroxysteroid 11 beta dehydrogenase 2
    • Hydroxysteroid 11 beta dehydrogenase isoenzyme 2
    • NAD dependent 11 beta hydroxysteroid dehydrogenase
    • NAD-dependent 11-beta-hydroxysteroid dehydrogenase
    • SDR9C3
    • Short chain dehydrogenase/reductase family 9C, member 3
    see all
  • 機能
    Catalyzes the conversion of cortisol to the inactive metabolite cortisone. Modulates intracellular glucocorticoid levels, thus protecting the nonselective mineralocorticoid receptor from occupation by glucocorticoids.
  • 組織特異性
    Found in placenta, kidney, pancreas, prostate, ovary, small intestine and colon.
  • 関連疾患
    Defects in HSD11B2 are the cause of apparent mineralocorticoid excess (AME) [MIM:218030]. AME is a potentially fatal disease characterized by severe juvenile low-renin hypertension, sodium retention, hypokalemia and low levels of aldosterone. It often leads to nephrocalcinosis.
  • 配列類似性
    Belongs to the short-chain dehydrogenases/reductases (SDR) family.
  • 細胞内局在
    Microsome. Endoplasmic reticulum.
  • Information by UniProt

画像

  • 12.5% SDS-PAGE Stained with Coomassie Blue

参考文献

ab114569 has not yet been referenced specifically in any publications.

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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"

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