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  4. SNRPN Antibody

SNRPN Antibody

  • 货号：
    CSB-PA022343GA01HU
  • 规格：
    ￥3,900
  • 其他：

产品详情

  • Uniprot No.：
    P63162
  • 基因名：
    SNRPN
  • 别名：
    HCERN3 antibody; PWCR antibody; RSMN_HUMAN antibody; RT LI antibody; RTLI antibody; SM D antibody; Sm N antibody; Sm protein D antibody; Sm protein N antibody; Sm-D antibody; Sm-N antibody; Small nuclear ribonucleoprotein associated protein N antibody; Small nuclear ribonucleoprotein polypeptide N antibody; Small nuclear ribonucleoprotein-associated protein N antibody; SMD antibody; SmN antibody; SNRNP N antibody; snRNP-N antibody; SNRNPN antibody; SNRPN antibody; SNURF SNRPN antibody; Tissue specific splicing protein antibody; Tissue-specific-splicing protein antibody
  • 宿主：
    Rabbit
  • 反应种属：
    Human,Mouse,Rat
  • 免疫原：
    Human SNRPN
  • 免疫原种属：
    Homo sapiens (Human)
  • 抗体亚型：
    IgG
  • 纯化方式：
    Antigen Affinity Purified
  • 浓度：
    It differs from different batches. Please contact us to confirm it.
  • 保存缓冲液：
    PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
  • 产品提供形式：
    Liquid
  • 应用范围：
    ELISA,WB,IHC,IF
  • 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：
    May be involved in tissue-specific alternative RNA processing events.
  • 基因功能参考文献：
    1. The first study reporting an association between variability in the SNRPN gene and the risk of being obese. PMID: 28387446
    2. we have confirmed that SNRPN methylation increases with age, which raises further questions regarding the role of SNRPN expression during the aging process. PMID: 26535694
    3. the cases with partial loss of methylation in KCNQ1OT1 and SNRPN present clinical features different to those associated with the corresponding imprinting syndromes PMID: 26106604
    4. Knockdown of SNRPN was demonstrated to significantly inhibit medulloblastoma cell growth and induce G2/M phase arrest in vitro. PMID: 25571951
    5. Data indicate that Sm nuclear antigen SmD-specific clonotypic IgGs showed extensive V- region hypermutation. PMID: 25577500
    6. indicate that SmN expression reduces the level of mature U2 snRNP, leading to alternative splicing PMID: 25238490
    7. The methylation patterns of the promoters of MTHFR and SNRPN are associated with changes in sperm motility and morphology, which could lead to male infertility. PMID: 24365028
    8. Human amniotic fluid mesenchymal stem cells contain a unique epigenetic signature during in vitro cell culture. H19 and KCNQ1OT1 possessed a substantial degree of hypermethylation status, and variable DNA methylation patterns of SNRPN was observed. PMID: 23040914
    9. In the skeletal muscle of neonate pigs, both NECD and SNRPN were maternally imprinted, while UBE3A was not imprinted. PMID: 22711311
    10. genetic association studies using 1,000 white subjects from Midwestern United States: Three copy number variations (CNV) in PWCR are associated with body fat mass, with a higher copy number (CN) associated with an increase of in body fat mass. PMID: 21233802
    11. Differences between genetic subtypes were also statistically significant in Prader Willi syndrome PMID: 21227640
    12. Variable methylation of the imprinted gene, SNRPN, supports a relationship between intracranial germ cell tumours and neural stem cells. PMID: 20582452
    13. SNRPN gene is imprinted, with monoallelic expression from the paternal allele in fetal brain and heart, and in adult brain. PMID: 7512861
    14. MEG3 and SNRPN genes are abnormally methylated in AML and MDS patients, and methylation of MEG3, but not SNRPN, confers worse overall prognosis. PMID: 19595458
    15. Methylation imprints of the imprint control region of the SPRPN-gene were studied in gametes and preimplantation embryos. ametes PMID: 14500540
    16. SMB and CD2BP2-GYF interact in the spliceosome PMID: 15105431
    17. Identification of cis- and trans-acting regulatory elements within the endogenous SNRPN 5' region. PMID: 16116039
    18. a possibly inactivating mutation in the SNRPN minimal promoter region was identified in Prader-Willi syndrome PMID: 17262171
    19. Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator) PMID: 18361419
    20. A mouse model for Prader-Willi syndrome. Deletion of Snrpn gene and putative imprinting-centre is associated with absent expression of the imprinted genes Zfp127, Ndn and Ipw, and phenotypes similar to those found in Prader-Willi infants. PMID: 9590284

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  • 亚细胞定位：
    Nucleus.
  • 蛋白家族：
    SnRNP SmB/SmN family
  • 组织特异性：
    Expressed in brain and lymphoblasts.
  • 数据库链接：

    HGNC: 11164

    OMIM: 182279

    KEGG: hsa:6638

    STRING: 9606.ENSP00000306223

    UniGene: Hs.564847