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PRSS12 Antibody

  • 货号：
    CSB-PA018812LA01HU
  • 规格：
    ￥440
  • 促销：
    小规格抗体限时一口价
  • 图片：
    • Immunohistochemistry of paraffin-embedded human brain tissue using CSB-PA018812LA01HU at dilution of 1:100
    • Immunohistochemistry of paraffin-embedded human lung tissue using CSB-PA018812LA01HU at dilution of 1:100
  • 其他：

产品详情

  • 产品名称：
    Rabbit anti-Homo sapiens (Human) PRSS12 Polyclonal antibody
  • Uniprot No.：
    P56730
  • 基因名：
    PRSS12
  • 别名：
    BSSP 3 antibody; BSSP3 antibody; Leydin antibody; MGC12722 antibody; Motopsin antibody; MRT1 antibody; NETR_HUMAN antibody; Neurotrypsin antibody; protease; serine; 12 (neurotrypsin; motopsin) antibody; Prss12 antibody; Serine protease 12 antibody
  • 宿主：
    Rabbit
  • 反应种属：
    Human
  • 免疫原：
    Recombinant Human Neurotrypsin protein (631-874AA)
  • 免疫原种属：
    Homo sapiens (Human)
  • 标记方式：
    Non-conjugated

    本页面中的产品，PRSS12 Antibody (CSB-PA018812LA01HU)，的标记方式是Non-conjugated。对于PRSS12 Antibody，我们还提供其他标记。见下表：

    可提供标记
    标记方式 货号 产品名称 应用
    HRP CSB-PA018812LB01HU PRSS12 Antibody, HRP conjugated ELISA
    FITC CSB-PA018812LC01HU PRSS12 Antibody, FITC conjugated
    Biotin CSB-PA018812LD01HU PRSS12 Antibody, Biotin conjugated ELISA
  • 克隆类型：
    Polyclonal
  • 抗体亚型：
    IgG
  • 纯化方式：
    >95%, Protein G purified
  • 浓度：
    It differs from different batches. Please contact us to confirm it.
  • 保存缓冲液：
    Preservative: 0.03% Proclin 300
    Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
  • 产品提供形式：
    Liquid
  • 应用范围：
    ELISA, IHC
  • 推荐稀释比：
    Application Recommended Dilution
    IHC 1:20-1:200
  • Protocols：
  • 储存条件：
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 货期：
    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.

产品评价

靶点详情

  • 功能：
    Plays a role in neuronal plasticity and the proteolytic action may subserve structural reorganizations associated with learning and memory operations.
  • 基因功能参考文献：
    1. 4-base pair deletion in the neurotrypsin gene was associated with autosomal recessive nonsyndromic mental retardation; findings suggest that neurotrypsin-mediated proteolysis is required for normal synaptic function PMID: 12459588
  • 相关疾病：
    Mental retardation, autosomal recessive 1 (MRT1)
  • 亚细胞定位：
    Secreted.
  • 蛋白家族：
    Peptidase S1 family
  • 组织特异性：
    Brain and Leydig cells of the testis.
  • 数据库链接：

    HGNC: 9477

    OMIM: 249500

    KEGG: hsa:8492

    STRING: 9606.ENSP00000296498

    UniGene: Hs.445857