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

BTD Antibody, Biotin conjugated

  • 中文名稱:
    BTD兔多克隆抗體, Biotin偶聯
  • 貨號:
    CSB-PA002854LD01HU
  • 規格:
    ¥880
  • 其他:

產品詳情

  • 產品名稱:
    Rabbit anti-Homo sapiens (Human) BTD Polyclonal antibody
  • Uniprot No.:
  • 基因名:
    BTD
  • 別名:
    Biotinase antibody; Biotinidase antibody; Btd antibody; BTD_HUMAN antibody; EC 3.5.1.12 antibody
  • 宿主:
    Rabbit
  • 反應種屬:
    Human
  • 免疫原:
    Recombinant Human Biotinidase protein (322-397AA)
  • 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:
    Catalytic release of biotin from biocytin, the product of biotin-dependent carboxylases degradation.
  • 基因功能參考文獻:
    1. BTD mutation is associated with biotinidase deficiency. PMID: 29995633
    2. Biotinidase deficiency is reviewed. PMID: 26577040
    3. Four rare missense variants were identified (ACTBL2 rs73757391 (5q11.2), BTD rs200337373 (3p25.1), KRT13 rs150321809 (17q21.2) and MC2R rs104894658 (18p11.21)), but only MC2R rs104894668 had a large effect size (OR = 9.66). PMID: 27378695
    4. The history and genetic basis of biotinidase deficiency has been presented. (Review) PMID: 26456103
    5. 48 novel alterations in the biotinidase gene have been identified; correlating the individual's serum enzymatic activity with genotype, were able to determine the effect of the novel alteration on enzyme activity and, thereby, determine its likelihood of being pathogenic in 44 of these individuals PMID: 26810761
    6. The common biotinidase gene mutations (p.R157H, p.D444H, c.98-104del7ins3, p.T532M) cumulatively accounted for 72.3% of all the mutant alleles in the Turkish population. PMID: 25754625
    7. Summary of the demographic features of patients identified as biotinidase deficient from August of 2012 through August of 2013 and mutation analysis results for 20 cases in the southeast region of Turkey. PMID: 25423671
    8. Three novel pathogenic variants in BTD gene were identified in a cohort of Brazilian patients with biotinidase deficiency and control suggesting an allelic heteregeneity of the condition. PMID: 25174816
    9. Report incidence of profound biotinase deficiency in Swedish newborns and adoptive immigrant children. PMID: 20224900
    10. High frequencies of biotinidase mutations may explain the high incidence of biotinidase deficiency in Hungary. PMID: 20549359
    11. Mutation analysis revealed three novel mutations, c.del631C and c.1557T>G within exon 4 and c.324-325insTA in exon 3 in Biotinidase deficiency patients and families. PMID: 23481307
    12. Four Somali patients have the P497S mutation, with one of the four being homozygous for the mutation PMID: 19757147
    13. Six different mutations in the biotinidase gene are identified in biotinidase in four Chinese patients; determination of biotinidase activities are performed for selective screening of biotinidase deficiency PMID: 19728141
    14. loss of overall biotinidase expression is a novel marker for thyroid cancer aggressiveness. PMID: 22911723
    15. Plasma BTD activity increases in hepatic glycogen storage disease patients. PMID: 20532819
    16. 140 known mutations in the biotinidase gene (BTD) that cause biotinidase deficiency, are reported. PMID: 20556795
    17. Mutations in biotinidase is associated with biotinidase deficiency. PMID: 20539236
    18. 12 patients with multiple carboxylase deficiency, six mutations were found in the BT gene and 4 in the HLCS gene, including 5 novel mutations. PMID: 19806568
    19. review of mutations causing biotinidase deficiency PMID: 11668630
    20. report of 17 novel mutations that cause profound biotinidase deficiency. Six of the mutations are due to deletions, whereas the remaining 11 mutations are missense mutations located throughout the gene PMID: 12359137
    21. analysis of mutations in biotinidase deficiency PMID: 15776412
    22. 21 different mutations were identified in 49 patients, including four novel mutations. Ten mutations proved to be unique to the Hungarian population. PMID: 17185019
    23. Posttranslational modification of histones by biotinylation can be catalyzed by biotinidase; role of this function is ambiguous. PMID: 18479898
    24. This case indicates that biotinidase deficiency should be included in the differential diagnosis of subacute myelopathy and emphasizes the importance of a prompt diagnosis to prevent irreversible neurological damage. PMID: 18645204

    顯示更多

    收起更多

  • 相關疾病:
    Biotinidase deficiency (BTD deficiency)
  • 亞細胞定位:
    Secreted, extracellular space.
  • 蛋白家族:
    Carbon-nitrogen hydrolase superfamily, BTD/VNN family
  • 數據庫鏈接:

    HGNC: 1122

    OMIM: 253260

    KEGG: hsa:686

    STRING: 9606.ENSP00000306477

    UniGene: Hs.444197



主站蜘蛛池模板: 老头边吃奶边弄进去呻吟| 欧美亚洲色aⅴ大片| 国产日韩欧美亚欧在线观看| 国产精品美女久久久久av爽 | 色婷婷综合久久久中文字幕| 色偷偷av男人的天堂| 成人无码男男gv在线观看网站| 久久久肥妇熟女ⅹxxx毛片| 日日碰狠狠丁香久燥| 久久人人玩人妻潮喷内射人人| 午夜理论片yy8860y影院| 无码天堂亚洲国产av麻豆| 中国熟女仑乱hd| 亚洲婷婷综合色高清在线| 国产农村乱对白刺激视频| 69成人免费视频无码专区| 69国产精品久久久久久人妻| 亚洲中文字幕无码中字| 99国产精品久久久蜜芽| 男人的天堂av社区在线| 欧美精品无码久久久久久| 亚洲成a人片在线观看www| 国产极品粉嫩馒头一线天av| 日韩少妇激情一区二区| 伊人久久大香线蕉av五月天宝贝| 少妇被粗大的猛烈进出免费视频| 亚洲色一色噜一噜噜噜 | 欧美成人国产精品高潮| 丁香色婷婷国产精品视频| 制服视频在线一区二区| 最新中文乱码字字幕在线| 伊伊综合在线视频无码| 免费无码一区二区三区蜜桃大| 亚洲精品av网站在线观看| 又色又爽又黄18禁美女裸身无遮挡| 日本高清视频www夜色资源| 无码中文字幕波多野结衣| 国产免费观看久久黄av片| 九色九九九老阿姨| av国産精品毛片一区二区网站 | 久久久久波多野结衣高潮|