Recombinant Human p57 Kip2 protein (ab112270)

製品の概要

  • 製品名Recombinant Human p57 Kip2 protein
  • タンパク質長Protein fragment

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P49918
    • 生物種Human
    • 配列MSDASLRSTSTMERLVARGTFPVLVRTSACRSLFGPVDHEELSRELQARL AELNAEDQNRWDYDFQQDMPLRGPGRLQWTEVDSDSVPAFYRETVQVGRC
    • 分子量37 kDa including tags
    • 領域1 to 100
    • タグGST tag N-Terminus

特性

Our Abpromise guarantee covers the use of ab112270 in the following tested applications.

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

  • 生理活性useful for Antibody Production and Protein Array
  • アプリケーション

    Peptide Array

    Western blot

    ELISA

    SDS-PAGE

  • 製品の状態Liquid
  • 備考Best use within three months from the date of receipt of this protein.useful for Antibody Production and Protein Array
  • 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: 0.79% Tris HCl, 0.31% Glutathione
    Note: Glutathione is reduced

関連情報

  • 別名
    • Beckwith Wiedemann syndrome
    • BWCR
    • BWS
    • CDKI
    • CDKN 1C
    • CDKN1C
    • CDN1C_HUMAN
    • Cyclin dependent kinase inhibitor 1C
    • Cyclin dependent kinase inhibitor p57
    • Cyclin-dependent kinase inhibitor 1C
    • Cyclin-dependent kinase inhibitor p57
    • KIP 2
    • KIP2
    • p57
    • p57 Kip 2
    • p57KIP2
    • WBS
    see all
  • 機能Potent tight-binding inhibitor of several G1 cyclin/CDK complexes (cyclin E-CDK2, cyclin D2-CDK4, and cyclin A-CDK2) and, to lesser extent, of the mitotic cyclin B-CDC2. Negative regulator of cell proliferation. May play a role in maintenance of the non-proliferative state throughout life.
  • 組織特異性Expressed in the heart, brain, lung, skeletal muscle, kidney, pancreas and testis. High levels are seen in the placenta while low levels are seen in the liver.
  • 関連疾患Defects in CDKN1C are a cause of Beckwith-Wiedemann syndrome (BWS) [MIM:130650]. BWS is a genetically heterogeneous disorder characterized by anterior abdominal wall defects including exomphalos (omphalocele), pre- and postnatal overgrowth, and macroglossia. Additional less frequent complications include specific developmental defects and a predisposition to embryonal tumors.
    Note=Defects in CDKN1C are involved in tumor formation.
  • 配列類似性Belongs to the CDI family.
  • 細胞内局在Nucleus.
  • Information by UniProt

Recombinant Human p57 Kip2 protein 画像

  • 12.5% SDS-PAGE Stained with Coomassie Blue.

Recombinant Human p57 Kip2 protein (ab112270) 使用論文

ab112270 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"