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COG7 Antibody

  • 中文名稱:
    COG7兔多克隆抗體
  • 貨號:
    CSB-PA005711GA01HU
  • 規格:
    ¥3,900
  • 其他:

產品詳情

  • Uniprot No.:
  • 基因名:
    COG7
  • 別名:
    CDG2E antibody; COG complex subunit 7 antibody; cog7 antibody; COG7_HUMAN antibody; Component of oligomeric Golgi complex 7 antibody; Conserved oligomeric Golgi complex component 7 antibody; Conserved oligomeric Golgi complex subunit 7 antibody
  • 宿主:
    Rabbit
  • 反應種屬:
    Human,Mouse,Rat
  • 免疫原:
    Human COG7
  • 免疫原種屬:
    Homo sapiens (Human)
  • 抗體亞型:
    IgG
  • 純化方式:
    Antigen Affinity Purified
  • 濃度:
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液:
    PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
  • 產品提供形式:
    Liquid
  • 應用范圍:
    ELISA,WB,IHC
  • Protocols:
  • 儲存條件:
    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.

產品評價

靶點詳情

  • 功能:
    Required for normal Golgi function.
  • 基因功能參考文獻:
    1. Cog5-Cog7 crystal structure reveals interactions essential for the function of a multisubunit tethering complex. PMID: 25331899
    2. COG5- and COG7 subunits play distinctive roles in controlling Golgi structure and function PMID: 16051600
    3. Retrograde transport of multiple Golgi proteins to the ER in COG-7-deficient patient fibroblasts via brefeldin A-induced tubules was significantly slower than occurs in normal fibroblasts. PMID: 16510524
    4. A homozygous, intronic splice site mutation (c.169+4A>C) of the COG7 gene was identified in 3 patients with Congenital Disorder of Glycosylation type IIe. PMID: 17356545
    5. A new mutation in COG7 extends the spectrum of COG subunit deficiencies. PMID: 19577670

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  • 相關疾病:
    Congenital disorder of glycosylation 2E (CDG2E)
  • 亞細胞定位:
    Golgi apparatus membrane; Peripheral membrane protein.
  • 蛋白家族:
    COG7 family
  • 數據庫鏈接:

    HGNC: 18622

    OMIM: 606978

    KEGG: hsa:91949

    STRING: 9606.ENSP00000305442

    UniGene: Hs.185807



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