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
      PDYVNGEVAATEA
    • 領域
      231 to 243

特性

Our Abpromise guarantee covers the use of ab28126 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

  • 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 or -80°C. Avoid repeated freeze / thaw cycles.

関連情報

  • 別名
    • HSPC046
    • LAB
    • LAT2
    • Linker for activation of B cells
    • Linker for activation of B-cells
    • Linker for activation of T cells family member 2
    • Linker for activation of T cells transmembrane adaptor 2
    • Linker for activation of T-cells family member 2
    • Membrane associated adapter molecule
    • Membrane-associated adapter molecule
    • Non T cell activation linker
    • Non-T-cell activation linker
    • NTAL_HUMAN
    • WBSCR 5
    • Wbscr15
    • Williams Beuren syndrome chromosome region 15
    • Williams Beuren syndrome chromosome region 5
    • Williams-Beuren syndrome chromosomal region 15 protein
    • Williams-Beuren syndrome chromosomal region 5 protein
    • WSCR5
    see all
  • 機能
    Involved in FCER1 (high affinity immunoglobulin epsilon receptor)-mediated signaling in mast cells. May also be involved in BCR (B-cell antigen receptor)-mediated signaling in B-cells and FCGR1 (high affinity immunoglobulin gamma Fc receptor I)-mediated signaling in myeloid cells. Couples activation of these receptors and their associated kinases with distal intracellular events through the recruitment of GRB2.
  • 組織特異性
    Highly expressed in spleen, peripheral blood lymphocytes, and germinal centers of lymph nodes. Also expressed in placenta, lung, pancreas and small intestine. Present in B-cells, NK cells and monocytes. Absent from T-cells (at protein level).
  • 関連疾患
    Note=LAT2 is located in the Williams-Beuren syndrome (WBS) critical region. WBS results from a hemizygous deletion of several genes on chromosome 7q11.23, thought to arise as a consequence of unequal crossing over between highly homologous low-copy repeat sequences flanking the deleted region. Haploinsufficiency of LAT2 may be the cause of certain cardiovascular and musculo-skeletal abnormalities observed in the disease.
  • 翻訳後修飾
    Phosphorylated on tyrosines following cross-linking of BCR in B-cells, FCGR1 in myeloid cells, or FCER1 in mast cells; which induces the recruitment of GRB2.
    May be polyubiquitinated.
  • 細胞内局在
    Cell membrane. Present in lipid rafts.
  • Information by UniProt

参考文献

ab28126 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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