在线日韩日本国产亚洲丨少妇伦子伦情品无吗丨欧美性猛交xxxx免费看蜜桃丨精品人妻系列无码一区二区三区丨亚洲精品无码不卡在线播放

Your Good Partner in Biology Research

POMGNT1 Antibody, FITC conjugated

  • 中文名稱:
    POMGNT1兔多克隆抗體, FITC偶聯
  • 貨號:
    CSB-PA855513LC01HU
  • 規格:
    ¥880
  • 其他:

產品詳情

  • 產品名稱:
    Rabbit anti-Homo sapiens (Human) POMGNT1 Polyclonal antibody
  • Uniprot No.:
  • 基因名:
    POMGNT1
  • 別名:
    2-N-acetylglucosaminyltransferase 1 antibody; 2-N-acetylglucosaminyltransferase I.2 antibody; GnT I.2 antibody; GnTI.2 antibody; MEB antibody; MGAT 1.2 antibody; MGAT1.2 antibody; O linked mannose beta1 2 N acetylglucosaminyltransferase antibody; PMGT1_HUMAN antibody; POMGNT 1 antibody; POMGnT1 antibody; Protein O linked mannose beta 1 2 N acetylglucosaminyltransferase 1 antibody; Protein O linked mannose beta1 2 N acetylglucosaminyltransferase antibody; Protein O-linked-mannose beta-1 antibody; UDP GlcNAc antibody; UDP GlcNAc:alpha D mannoside beta 1 2 N acetylglucosaminyltransferase I.2 antibody; UDP-GlcNAc:alpha-D-mannoside beta-1 antibody
  • 宿主:
    Rabbit
  • 反應種屬:
    Human
  • 免疫原:
    Recombinant Human Protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1 protein (59-300AA)
  • 免疫原種屬:
    Homo sapiens (Human)
  • 標記方式:
    FITC
  • 克隆類型:
    Polyclonal
  • 抗體亞型:
    IgG
  • 純化方式:
    >95%, Protein G purified
  • 濃度:
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液:
    Preservative: 0.03% Proclin 300
    Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
  • 產品提供形式:
    Liquid
  • 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:
    Participates in O-mannosyl glycosylation by catalyzing the addition of N-acetylglucosamine to O-linked mannose on glycoproteins. Catalyzes the synthesis of the GlcNAc(beta1-2)Man(alpha1-)O-Ser/Thr moiety on alpha-dystroglycan and other O-mannosylated proteins, providing the necessary basis for the addition of further carbohydrate moieties. Is specific for alpha linked terminal mannose and does not have MGAT3, MGAT4, MGAT5, MGAT7 or MGAT8 activity.
  • 基因功能參考文獻:
    1. These findings demonstrate that PomGnT1 might be a new focus of glioblastoma (GBM)research for treatment of recurrent Temozolomide -resistant GBM PMID: 29048655
    2. The authors have identified a novel mutation in POMGNT1 that causes nonsyndromic autosomal recessive retinitis pigmentosa, adding to the genetic heterogeneity of this retinal disease. PMID: 27391550
    3. Study identified recessive POMGNT1 mutations in three unrelated non-syndromic retinitis pigmentosa families showing significant impaired POMGNT1 enzymatic activity. PMID: 26908613
    4. When association tests were applied to data from the Diabetes Heart Study, it found exome variants of POMGNT1 and JAK1 genes were associated with type 2 diabetes. PMID: 26783077
    5. POMGNT1 Is Glycosylated by Mucin-Type O-Glycans PMID: 26328495
    6. study presents clinical, neuroradiological, and POMGNT1 findings in 12 muscle-eye-brain disease patients of Turkish origin from 10 families; suggests a genotype-phenotype correlation PMID: 24731844
    7. Data indicate that Golgi phosphoprotein 3 (GOLPH3) binds to and controls the Golgi localization of protein O-linked mannose beta-1,2-N-acetlyglucosaminyltransferase 1 (POMGnT1). PMID: 24733390
    8. Identification of novel POMGnT1 mutations in Chinese patients with muscle-eye-brain disease. PMID: 23689641
    9. POMGnT1 point mutations and protein expression are associated with variably severe muscle-eye-brain disease showing that severity of the phenotype does not correlate with protein expression. PMID: 22554691
    10. Promoter alteration causes transcriptional repression of the POMGNT1 gene in limb-girdle muscular dystrophy type 2O. PMID: 22419172
    11. This study demonistreated that Intragenic rearrangements in POMGNT1 gene in muscle-eye-brain disease. PMID: 21727005
    12. these results show that the amino acid sequence affects POMGnT1 activity. PMID: 21684258
    13. This study gives a comprehensive biochemical evaluation of all clinically relevant POMGnT1 point mutations known to date, which have been linked to muscle-eye-brain disease or similar conditions. PMID: 21361872
    14. the function of the gene products is only known for POMT1, POMT2, and POMGnT1, all responsible for the O-mannosylglycan biosynthesis PMID: 20816175
    15. Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts, unlinked to the MEB locus, in three Tunisian patients PMID: 12467726
    16. Loss-of-function of an N-acetylglucosaminyltransferase, POMGnT1, in muscle-eye-brain disease. 13 mutations have been identified in patients with MEB. The mutant POMGnT1s were expressed and none had any activity. PMID: 12788071
    17. Results describe the identification of a novel O-linked mannose beta1,2-N-acetylglucosaminyltransferase (POMGnT1) gene missense mutation in muscle-eye-brain disease. PMID: 15236414
    18. DNA mutational analysis and phenotypes in patients with muscle-eye-brain disease PMID: 15466003
    19. Our results suggest that PomGnT1, enzymes involved in the O-mannosyl glycosylation pathway, play an active role in modulating integrin and laminin-dependent adhesion and migration of human neuronal cells. PMID: 16857188
    20. In conclusion, the lymphoblast-based enzymatic assay is a sensitive and useful method (i) to select patients harbouring POMGNT1, POMT1 or POMT2 mutations; (ii) to assess the pathogenicity of new or already described mutations. PMID: 17869517
    21. report on two Turkish siblings with a homozygous mutation in the POMGnT1 gene; a 6-year-old sibling has a severe form of muscle-eye-brain (MEB) disease; the same mutation resulted in a less severe form of MEB in the older sibling PMID: 17881266
    22. data suggest mutational hotspots within the minimal catalytic domain at arginine residue 442 (exon 16) and in intron 17 PMID: 17906881

    顯示更多

    收起更多

  • 相關疾病:
    Muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies A3 (MDDGA3); Muscular dystrophy-dystroglycanopathy congenital with mental retardation B3 (MDDGB3); Muscular dystrophy-dystroglycanopathy limb-girdle C3 (MDDGC3); Retinitis pigmentosa 76 (RP76)
  • 亞細胞定位:
    Golgi apparatus membrane; Single-pass type II membrane protein.
  • 蛋白家族:
    Glycosyltransferase 13 family
  • 組織特異性:
    Constitutively expressed. An additional weaker band is also detected in spinal cord, lymph node, and trachea. Expressed especially in astrocytes. Also expressed in immature and mature neurons.
  • 數據庫鏈接:

    HGNC: 19139

    OMIM: 253280

    KEGG: hsa:55624

    STRING: 9606.ENSP00000361052

    UniGene: Hs.525134



主站蜘蛛池模板: 日韩精品久久久免费观看| 免费香蕉成视频人网站| 免费国产在线精品一区不卡| 中文无码av在线亚洲电影| 夜夜高潮夜夜爽夜夜爱| 欧美一区二区三区激情| 日韩成人无码毛片一区二区| 国产亚洲精品久久久久久彩霞| 国产精品视频一区二区三区不卡| 人妻丰满熟妞av无码区| 欧美人牲口杂交在线播放免费| 亚洲色欲色欲77777小说网站| 日本一区二区三区免费播放| 亚洲精品久久久中文字幕痴女| 中文字幕日本特黄aa毛片| 精品日产一卡二卡| 国产在线观看无码免费视频| 日韩欧美人妻一区二区三区| 亚洲国产精品久久久久婷婷软件| 国产美女裸身网站免费观看视频| 377人体粉嫩噜噜噜| 欧美国产国产综合视频| 成年奭片免费观看视频天天看 | 男男车车的车车网站w98免费| 色五月五月丁香亚洲综合网| 秋霞最新高清无码鲁丝片| 狠日狠干日日射| 污污内射久久一区二区欧美日韩| 伊人情人色综合网站| 精品一卡2卡三卡4卡乱码精品视频| 日本黄网站免费| 成人亚洲欧美成αⅴ人在线观看| 国产成人精品免费视频大全五级| 伊人精品成人久久综合97 | 国产成人久久av免费| 精品国产sm最大网免费站 | 国产日韩一区二区三区在线观看| 99久久国产露脸国语对白 | 久久精品夜色噜噜亚洲a∨| 国产高清在线精品一区小说| 久久丫精品系列|