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Your Good Partner in Biology Research

PGAP2 Antibody, HRP conjugated

  • 中文名稱:
    PGAP2兔多克隆抗體, HRP偶聯(lián)
  • 貨號(hào):
    CSB-PA883397LB01HU
  • 規(guī)格:
    ¥880
  • 其他:

產(chǎn)品詳情

  • 產(chǎn)品名稱:
    Rabbit anti-Homo sapiens (Human) PGAP2 Polyclonal antibody
  • Uniprot No.:
  • 基因名:
    PGAP2
  • 別名:
    PGAP2; FRAG1; Post-GPI attachment to proteins factor 2; FGF receptor-activating protein 1
  • 宿主:
    Rabbit
  • 反應(yīng)種屬:
    Human
  • 免疫原:
    Recombinant Human Post-GPI attachment to proteins factor 2 protein (45-114AA)
  • 免疫原種屬:
    Homo sapiens (Human)
  • 標(biāo)記方式:
    HRP
  • 克隆類型:
    Polyclonal
  • 抗體亞型:
    IgG
  • 純化方式:
    >95%, Protein G purified
  • 濃度:
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液:
    Preservative: 0.03% Proclin 300
    Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
  • 產(chǎn)品提供形式:
    Liquid
  • 應(yīng)用范圍:
    ELISA
  • Protocols:
  • 儲(chǔ)存條件:
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 貨期:
    Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
  • 用途:
    For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產(chǎn)品評價(jià)

靶點(diǎn)詳情

  • 功能:
    Involved in the lipid remodeling steps of GPI-anchor maturation. Required for stable expression of GPI-anchored proteins at the cell surface.
  • 基因功能參考文獻(xiàn):
    1. A Rare Variant in PGAP2 Causes Autosomal Recessive Hyperphosphatasia with Mental Retardation Syndrome, with a Mild Phenotype in Heterozygous Carriers. PMID: 29119105
    2. Hypomorphic mutations in PGAP2, encoding a GPI-anchor-remodeling protein, cause autosomal-recessive intellectual disability. PMID: 23561846
    3. PGAP2 mutations, affecting the GPI-anchor-synthesis pathway, cause hyperphosphatasia with mental retardation syndrome. PMID: 23561847
  • 相關(guān)疾病:
    Hyperphosphatasia with mental retardation syndrome 3 (HPMRS3)
  • 亞細(xì)胞定位:
    Golgi apparatus membrane; Multi-pass membrane protein. Endoplasmic reticulum membrane; Multi-pass membrane protein.
  • 蛋白家族:
    PGAP2 family
  • 組織特異性:
    Ubiquitously expressed, with highest levels in testis and pancreas.
  • 數(shù)據(jù)庫鏈接:

    HGNC: 17893

    OMIM: 614207

    KEGG: hsa:27315

    STRING: 9606.ENSP00000278243

    UniGene: Hs.133968



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