製品の概要

製品の詳細

  • 由来Synthetic
  • アミノ酸配列
    • 生物種Human
    • 配列C-RARQSLGTGTLVS
    • 領域115 to 127

関連製品

特性

Our Abpromise guarantee covers the use of ab45560 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

    Blocking - Blocking peptide for Anti-PHLDA3 antibody (ab22822)

  • 製品の状態Liquid
  • Concentration information loading...

前処理および保存

  • 保存方法および安定性

    Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.

関連情報

  • 別名
    • PHLA3_HUMAN
    • PHLDA 3
    • phlda3
    • Pleckstrin homology like domain family A member 2
    • Pleckstrin homology like domain family A member 3
    • Pleckstrin homology-like domain family A member 3
    • TDAG51/Ipl homolog 1
    • TDAG51/Ipl homologue 1
    • TIH 1
    • TIH1
    see all
  • 機能p53/TP53-regulated repressor of Akt/AKT1 signaling. Represses AKT1 by preventing AKT1-binding to membrane lipids, thereby inhibiting AKT1 translocation to the cellular membrane and activation. Contributes to p53/TP53-dependent apoptosis by repressing AKT1 activity. Its directs transcription regulation by p53/TP53 may explain how p53/TP53 can negatively regulate AKT1. May acts as a tumor suppressor.
  • 組織特異性Widely expressed with lowest expression in liver and spleen.
  • 配列類似性Belongs to the PHLDA3 family.
    Contains 1 PH domain.
  • ドメインThe PH domain binds phosphoinositides with a broad specificity. It competes with the PH domain of AKT1 and directly interferes with AKT1 binding to phosphatidylinositol 4,5-bisphosphate (PIP2) and phosphatidylinositol 3,4,5-triphosphate (PIP3), preventing AKT1 association to membrane lipids and subsequent activation of AKT1 signaling.
  • 細胞内局在Cytoplasm. Membrane.
  • Information by UniProt

Human PHLDA3 peptide (ab45560) 使用論文

ab45560 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"