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TSPYL1 Antibody

  • 货号：
    CSB-PA288008
  • 规格：
    ￥1100
  • 图片：
    • Gel: 8%SDS-PAGE,Lysate: 40 μg,,Primary antibody: CSB-PA288008(TSPYL1 Antibody) at dilution 1/200 dilution,Secondary antibody: Goat anti rabbit IgG at 1/8000 dilution,Exposure time: 2 minutes
  • 其他：

产品详情

  • Uniprot No.：
    Q9H0U9
  • 基因名：
    TSPYL1
  • 别名：
    SIDDT antibody; Testis specific like protein Y encoded antibody; Testis specific Y encoded like protein 1 antibody; Testis-specific Y-encoded-like protein 1 antibody; TSPY like antibody; TSPY like 1 antibody; TSPY like protein 1 antibody; TSPY-like protein 1 antibody; TSPYL antibody; TSPYL1 antibody; TSYL1_HUMAN antibody
  • 宿主：
    Rabbit
  • 反应种属：
    Human,Mouse
  • 免疫原：
    Synthetic peptide of Human TSPYL1
  • 免疫原种属：
    Homo sapiens (Human)
  • 标记方式：
    Non-conjugated
  • 抗体亚型：
    IgG
  • 纯化方式：
    Antigen affinity purification
  • 浓度：
    It differs from different batches. Please contact us to confirm it.
  • 保存缓冲液：
    -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
  • 产品提供形式：
    Liquid
  • 应用范围：
    ELISA,WB
  • 推荐稀释比：
    Application Recommended Dilution
    ELISA 1:1000-1:2000
    WB 1:200-1:1000
  • 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

  • 基因功能参考文献：
    1. Results show that mutations and polymorphisms in the TSPYL1 gene were not associated with sudden infant death syndrome in a cohort of 165 deceased Swiss infants. PMID: 25449952
    2. Mutations in the TSPYL1 gene do not seem to play a major role in the pathogenesis of idiopathic male infertility, and mutation screening of the TSPYL1 gene can currently not be recommended in routine diagnostics of idiopathic male infertility. PMID: 22137496
    3. The chromatin remodeling factor TSPYL1 had a very similar pattern of expression with an incremental increase in HPFH and decreased expression in deltabeta-thalassemia. PMID: 16952470
    4. Mutations in TSPYL1 may contribute to anomalies of testicular development/function. PMID: 19463995
  • 相关疾病：
    Sudden infant death with dysgenesis of the testes syndrome (SIDDT)
  • 亚细胞定位：
    Nucleus, nucleolus.
  • 蛋白家族：
    Nucleosome assembly protein (NAP) family
  • 组织特异性：
    Expressed in testis, ovary, liver, spleen, brain, kidney, prostate, lung, liver, and heart.
  • 数据库链接：

    HGNC: 12382

    OMIM: 604714

    KEGG: hsa:7259

    STRING: 9606.ENSP00000357597

    UniGene: Hs.458358