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

  • 中文名稱:
    HEXA兔多克隆抗體
  • 貨號:
    CSB-PA005178
  • 規格:
    ¥1090
  • 圖片:
    • Western Blot analysis of HepG2 cells using HEXA Polyclonal Antibody
  • 其他:

產品詳情

  • 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,Mouse,Rat
  • 免疫原:
    Synthesized peptide derived from the Internal region of Human HEXA.
  • 免疫原種屬:
    Homo sapiens (Human)
  • 標記方式:
    Non-conjugated
  • 抗體亞型:
    IgG
  • 純化方式:
    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 濃度:
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液:
    Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 產品提供形式:
    Liquid
  • 應用范圍:
    WB, ELISA
  • 推薦稀釋比:
    Application Recommended Dilution
    WB 1:500-1:2000
    ELISA 1:20000
  • 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: 日韩人妻熟女中文字幕aⅴ春菜| 国产孩cao大人xxxx| 国语自产精品视频在 视频| 亚洲 制服 丝袜 无码 在线| 女高中生自慰污污网站| 亚洲成av人片一区二区梦乃| 国产又黄又猛又粗又爽的a片动漫| 亚洲一区av无码少妇电影| 亚洲第一成年免费网站| 天天爱天天做久久狠狠做| 日本三级在线播放线观看视频| 亚洲a∨无码一区二区三区| 亚洲欧美国产精品久久| 三男一女吃奶添下面视频| 天天看片视频免费观看| 无码中出人妻中文字幕av | 一边吃奶一边添p好爽高清视频| 欧美日韩亚洲精品瑜伽裤| 乱码av麻豆丝袜熟女系列| 国产亚洲视频在线观看播放| 国产精品久久人妻无码网站蜜臀| 精品综合久久久久久97| 搡老女人老妇女老熟妇| 亚洲成a人片在线观看中文| 国产初高中生粉嫩无套第一次| 国精品99久9在线 | 免费| 伊人久久大香线蕉av网| 后入内射国产一区二区| 性按摩xxxx在线观看| 午夜福利18以下勿进免费| 纯肉无遮挡h肉动漫在线观看国产 国产精品18久久久久久欧美 | 曰本av中文字幕一区二区| 日本大乳高潮视频在线观看| 国语自产拍精品香蕉在线播放| 夜夜夜夜猛噜噜噜噜噜试看| 草的我好爽视频| 国产一区二区三区四区五区加勒比| 新版天堂资源中文www连接| 亚洲综合精品香蕉久久网| 日韩人妻精品无码一区二区三区| 久久久久久人妻一区二区三区|