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

HEXA Antibody, Biotin conjugated

  • 中文名稱:
    HEXA兔多克隆抗體, Biotin偶聯
  • 貨號:
    CSB-PA12259D0Rb
  • 規格:
    ¥880
  • 其他:

產品詳情

  • 產品名稱:
    Rabbit anti-Homo sapiens (Human) HEXA Polyclonal antibody
  • Uniprot No.:
  • 基因名:
  • 別名:
    Beta hexosaminidase alpha chain precursor antibody; Beta hexosaminidase subunit alpha antibody; Beta N acetylhexosaminidase antibody; Beta N acetylhexosaminidase subunit alpha antibody; Beta-hexosaminidase A antibody; Beta-hexosaminidase subunit alpha antibody; Beta-N-acetylhexosaminidase subunit alpha antibody; Hexa antibody; HEXA_HUMAN antibody; Hexosaminidase A (alpha polypeptide) antibody; Hexosaminidase A alpha polypeptide antibody; Hexosaminidase A antibody; Hexosaminidase subunit A antibody; MGC99608 antibody; N acetyl beta glucosaminidase antibody; N acetyl beta glucosaminidase subunit alpha antibody; N-acetyl-beta-glucosaminidase subunit alpha antibody; TSD antibody
  • 宿主:
    Rabbit
  • 反應種屬:
    Human
  • 免疫原:
    Recombinant Human Beta-hexosaminidase subunit alpha protein (89-529AA)
  • 免疫原種屬:
    Homo sapiens (Human)
  • 標記方式:
    Biotin
  • 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
  • 應用范圍:
    ELISA
  • Protocols:
  • 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:
    Hydrolyzes the non-reducing end N-acetyl-D-hexosamine and/or sulfated N-acetyl-D-hexosamine of glycoconjugates, such as the oligosaccharide moieties from proteins and neutral glycolipids, or from certain mucopolysaccharides. The isozyme S is as active as the isozyme A on the anionic bis-sulfated glycans, the chondroitin-6-sulfate trisaccharide (C6S-3), and the dermatan sulfate pentasaccharide, and the sulfated glycosphingolipid SM2. The isozyme B does not hydrolyze each of these substrates, however hydrolyzes efficiently neutral oligosaccharide. Only the isozyme A is responsible for the degradation of GM2 gangliosides in the presence of GM2A.
  • 基因功能參考文獻:
    1. Reported data present, for the first time, reference values for urinary activities of HEX and its isoenzymes HEX A and HEX B in children and adolescent. PMID: 28846871
    2. The alpha mutants E482K and G269S are defective in enzymatic activity, unprocessed by lysosomal proteases, and exhibit altered folding pathways compared with wild-type alpha. E482K is more severely misfolded than G269S, as observed by its aggregation and inability to associate with the HexA beta chain. Importantly, both mutants are retrotranslocated from the endoplasmic reticulum to the cytosol and are degraded by the ... PMID: 27682588
    3. reports a new missense mutation in the HEXA gene in two German siblings with late-onset Tay-Sachs disease and prominent psychiatric symptoms PMID: 25860343
    4. The silencing of the HEXA gene had a stronger immune inhibitory effect, thereby indicating a major involvement of beta-N-acetyl-hexosaminidase A isoenzyme within this mechanism. PMID: 21997228
    5. Human prostate cancer cells are characterised by a significant decrease in HexA activity. PMID: 24389457
    6. DNA reveals novel mutations in Iranian subjects causing Tay-Sachs disease in the alpha and beta subunits of HexA. PMID: 24518553
    7. GM2 gangliosidosis is caused by the gene mutation. (review) PMID: 23370522
    8. Identification of six novel missense mutations in children affected with Tay Sachs disease from India. PMID: 22723944
    9. identified 27 different mutations, 14 of which were novel, in the HEXA gene and 14 different mutations, 8 of which unreported until now, in the HEXB gene, and attempted to correlate these mutations with the clinical presentation of the patients PMID: 22789865
    10. MtsD, MtsF and MtsH are fusion proteins with a methyltransferase domain and a corrinoid-binding domain. PMID: 19732345
    11. HEXA gene in Argentinean patients affected with Tay-Sachs disease, overall 14 different mutations were identified, 8 of them were novel and lead to premature stop codons, drastic residues changes or a splicing defect. PMID: 22441121
    12. Beta-hexosaminidase over-expression affects lysosomal glycohydrolases expression and glycosphingolipid metabolism in mammalian cells. PMID: 22147196
    13. We report the first Jordanian Arab Tay-Sachs disease patient diagnosed by deficient beta-hexosaminidase A activity, mutation analysis revealed homozygosity for a nonsense HEXA mutation, c.78G>A (p.W26X) PMID: 21967858
    14. Two mutations were identified c.1A>G (p.MIV), which obliterated the initiating methionine in codon 1, and c.1177C>T (p.R393X), which predicted a termination codon or nonsense mutation in infantile Tay-Sachs diseae in the Persian population. PMID: 21796138
    15. Down-regulation of beta-N-acetyl-D-glucosaminidase increases Akt1 activity in thyroid anaplastic cancer cells PMID: 21637923
    16. Detected mutations in the HEXA gene through gene sequencing and, by combining the HEXA enzyme assay and the HEXA gene sequencing assay, were able to clarify Tay Sachs carrier status. PMID: 19858779
    17. Eight novel mutations PMID: 12180151
    18. plasma activity of total Hex does not appear to be a reliable marker of erosion and cartilage degradation in rheumatoid arthritis patients; liver function appears to be the major determinant for the plasma Hex activity in these patients PMID: 12413610
    19. second novel HEXA mutation specific to the IJ TDS carriers: a substitution of cytosine 1351 by guanosine (C1351G), resulting in the change of leucine to valine in position 451. PMID: 14648242
    20. the founder effect in a rapidly expanding population arising from a bottleneck provides a robust parsimonious hypothesis explaining the spread of 1278insTATC-linked TSD in Ashkenazi Jews PMID: 14727180
    21. Therefore, our bicistronic lentivector supplying both alpha- and beta-subunits of beta-hexosaminidases may provide a potential therapeutic tool for the treatment of Sandhoff disease. PMID: 15953731
    22. analysis of the HEXA gene in Italian patients with infantile and late onset Tay-Sachs disease PMID: 16088929
    23. The plasma membrane associated beta-hexosaminidase A is fully processed, suggesting its lysosomal origin. PMID: 16212960
    24. the X-ray crystallographic structure of Hex A to 2.8 A resolution. The crystal structure of Hex A reveals an alphabeta heterodimer, with each subunit having a functional active site PMID: 16698036
    25. The highest activities of exoglycosidases were observed in high-grade gliomas, and a positive correlation of enzyme activities and degree of malignancy was noted. PMID: 16710745
    26. isoenzyme composition of N-acetyl-beta-D-hexosaminidase in seminal plasma from patients with secretory azoospermia is significantly different from controls, but this difference does not represent a useful marker of secretory azoospermia PMID: 16776631
    27. Describe strategy for detecting HexA mutations/activity in prenatal diagnosis of Tay-Sachs disease. PMID: 18425478
    28. In the infantile Tay-Sachs group, the number of atoms influenced by a mutation was larger than that in the late-onset disease group. PMID: 18490185
    29. A significantly higher activity of N-acetyl-beta-D-hexosaminidase in all laryngeal cancer specimens compared with that in healthy tissue homogenates, was observed. PMID: 19298806

    顯示更多

    收起更多

  • 相關疾病:
    GM2-gangliosidosis 1 (GM2G1)
  • 亞細胞定位:
    Lysosome.
  • 蛋白家族:
    Glycosyl hydrolase 20 family
  • 數據庫鏈接:

    HGNC: 4878

    OMIM: 272800

    KEGG: hsa:3073

    STRING: 9606.ENSP00000268097

    UniGene: Hs.604479



主站蜘蛛池模板: 国产+日韩+另类+视频一区| 69风韵老熟女口爆吞精| 最新精品国偷自产在线老年人| 97国产色伦在色在线播放| 一本加勒比hezyo中文无码| 少妇又色又紧又爽又刺激视频| 久久99国产综合精品| 免费国精产品自偷自偷免费看| 日韩久久无码免费毛片软件| 日本公与熄乱理在线播放| 亚洲欧洲国产综合aⅴ无码| 欧美 日本 国产 在线a∨观看| 中文字幕无码精品亚洲资源网久久| 欧美成人一区二区三区片免费| 久久亚洲一区二区三区四区| 伊人蕉久中文字幕无码专区| 蜜桃日本免费观看mv| 亚洲国产天堂久久综合网| 少妇又紧又深又湿又爽视频| 韩国乱码伦视频免费| 强行交换配乱婬bd| 国产成人亚洲高清一区| 国产国拍亚洲精品av| 图片区小说区av区| 国产精品国产三级国产av主播| 国产精品久久久久久久久人妻| 色又黄又爽18禁免费视频| 国产亚洲精aa在线观看see| 国内精品久久久久av福利秒拍| 国产精品99久久久久久人| 日韩人妻中文无码一区二区七区| 国产精品嫩草影院久久| 日韩在线看片免费人成视频播放 | 色哟哟国产精品免费观看| 蜜臀av99无码精品国产专区| 亚洲欧美不卡高清在线观看| 激情综合色五月丁香六月欧美| …日韩人妻无码精品一专区| 日本又色又爽又黄的视频免| 人妻熟女久久久久久久| 精品人妻系列无码一区二区三区 |