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SLC35A1 Antibody

  • 中文名稱:
    SLC35A1兔多克隆抗體
  • 貨號(hào):
    CSB-PA021583ESR1HU
  • 規(guī)格:
    ¥440
  • 圖片:
    • Immunohistochemistry of paraffin-embedded human spleen tissue using CSB-PA021583ESR1HU at dilution of 1:100
  • 其他:

產(chǎn)品詳情

  • 產(chǎn)品名稱:
    Rabbit anti-Homo sapiens (Human) SLC35A1 Polyclonal antibody
  • Uniprot No.:
  • 基因名:
    SLC35A1
  • 別名:
    CMP-SA-Tr antibody; CMP-Sia-Tr antibody; CMP-sialic acid transporter antibody; S35A1_HUMAN antibody; Slc35a1 antibody; Solute carrier family 35 member A1 antibody
  • 宿主:
    Rabbit
  • 反應(yīng)種屬:
    Human
  • 免疫原:
    Recombinant Human CMP-sialic acid transporter protein (1-100AA)
  • 免疫原種屬:
    Homo sapiens (Human)
  • 標(biāo)記方式:
    Non-conjugated
  • 克隆類型:
    Polyclonal
  • 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 0.02% sodium azide, 50% glycerol, pH7.3.
  • 產(chǎn)品提供形式:
    Liquid
  • 應(yīng)用范圍:
    ELISA, IHC
  • 推薦稀釋比:
    Application Recommended Dilution
    IHC 1:20-1:200
  • 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(píng)價(jià)

靶點(diǎn)詳情

  • 功能:
    Transports CMP-sialic acid from the cytosol into Golgi vesicles where glycosyltransferases function. Efficient CMP-sialic acid uptake depends on the presence of free CMP inside the vesicles, suggesting the proteins functions as an antiporter. Binds both CMP-sialic acid and free CMP, but has higher affinity for free CMP.
  • 基因功能參考文獻(xiàn):
    1. We performed exome sequencing on an individual with a profound neurological presentation and identified rare compound heterozygous mutations, p.Thr156Arg and p.Glu196Lys, in the CMP-sialic acid transporter, SLC35A1. Patient primary fibroblasts and serum showed a considerable decrease in the amount of N- and O-glycans terminating in sialic acid PMID: 28856833
    2. the SLC35A1 generates additional isoforms through alternative splicing. PMID: 27387429
    3. SLC35A1-deficient cells lack of alpha-dystroglycan O-mannosylation, ligand binding and incorporation of sialic acids. PMID: 25552652
    4. We confirm an autosomal recessive, generalized sialylation defect due to mutations in SLC35A1 PMID: 23873973
    5. substrate binding specificity PMID: 12682060
    6. this defect is a new type of congenital disorder of glycosylation (CDG) of type IIf affecting the transport of CMP-sialic acid into the Golgi apparatus. PMID: 15576474
    7. this study, we introduced two critical genes encoding human CMP-N-acetylneuraminic acid synthetase and CMP-sialic acid transporter into tobacco suspension-cultured cell to pave a route for sialic biosynthetic pathway. PMID: 16343442
    8. CMP-sialic acid transporter is localized in the medial-trans Golgi PMID: 16923816

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  • 相關(guān)疾病:
    Congenital disorder of glycosylation 2F (CDG2F)
  • 亞細(xì)胞定位:
    Golgi apparatus membrane; Multi-pass membrane protein.
  • 蛋白家族:
    Nucleotide-sugar transporter family, SLC35A subfamily
  • 數(shù)據(jù)庫鏈接:

    HGNC: 11021

    OMIM: 603585

    KEGG: hsa:10559

    STRING: 9606.ENSP00000358565

    UniGene: Hs.423163



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