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

inhA Antibody, HRP conjugated

Rare Species
  • 中文名稱:
    inhA兔多克隆抗體, HRP偶聯
  • 貨號:
    CSB-PA363781HB01MVZ
  • 規格:
    ¥880
  • 其他:

產品詳情

  • 產品名稱:
    Rabbit anti-Mycobacterium tuberculosis inhA Polyclonal antibody
  • Uniprot No.:
  • 基因名:
    inhA
  • 別名:
    inhA antibody; Rv1484 antibody; MTCY277.05 antibody; Enoyl-[acyl-carrier-protein] reductase [NADH] antibody; ENR antibody; Enoyl-ACP reductase antibody; EC 1.3.1.9 antibody; FAS-II enoyl-ACP reductase antibody; NADH-dependent 2-trans-enoyl-ACP reductase antibody
  • 宿主:
    Rabbit
  • 反應種屬:
    Mycobacterium tuberculosis
  • 免疫原:
    Recombinant Mycobacterium tuberculosis Enoyl-[acyl-carrier-protein] reductase [NADH] protein (1-269AA)
  • 免疫原種屬:
    Mycobacterium tuberculosis
  • 標記方式:
    HRP
  • 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:
    Enoyl-ACP reductase of the type II fatty acid syntase (FAS-II) system, which is involved in the biosynthesis of mycolic acids, a major component of mycobacterial cell walls. Catalyzes the NADH-dependent reduction of the double bond of 2-trans-enoyl-[acyl-carrier protein], an essential step in the fatty acid elongation cycle of the FAS-II pathway. Shows preference for long-chain fatty acyl thioester substrates (>C16), and can also use 2-trans-enoyl-CoAs as alternative substrates. The mycobacterial FAS-II system utilizes the products of the FAS-I system as primers to extend fatty acyl chain lengths up to C56, forming the meromycolate chain that serves as the precursor for final mycolic acids.; Is the primary target of the first-line antitubercular drug isoniazid (INH) and of the second-line drug ethionamide (ETH). Overexpressed inhA confers INH and ETH resistance to M.tuberculosis. The mechanism of isoniazid action against InhA is covalent attachment of the activated form of the drug to the nicotinamide ring of NAD and binding of the INH-NAD adduct to the active site of InhA. Similarly, the ETH-NAD adduct binds InhA.
  • 基因功能參考文獻:
    1. Out of the 141 isolates studied, 3 (2.1%) were found carrying mutations in the katG gene that confer resistance to Isoniazid (INH). No mutations were detected in the inhA promoter region gene that confer weak INH resistance or in the rpoB gene that confer Rifampicin resistance. PMID: 29868151
    2. Molecular dynamics (MD) simulation show that EN and N1 remained in the binding pocket similar to the docked pose of EN-InhA and E1-InhA complexes and also suggested that InhA binds to its inhibitor in inhibitor-induced folding manner. Our study concludes that multiple receptor conformers based molecular docking can be an alternative to study the effect of receptor flexibility in ligand binding PMID: 28957755
    3. Virtually Designed Triclosan-Based Inhibitors of Enoyl-Acyl Carrier Protein Reductase of Mycobacterium tuberculosis and of Plasmodium falciparum. PMID: 27490275
    4. Structural analysis of InhA provided the crucial points to enhance the NADH binding affinity towards InhA mutants in the presence of direct InhA inhibitors to combat isoniazid drug resistance. PMID: 26658674
    5. InhA gene mutation is associated with isoniazid resistance in Mycobacterium tuberculosis. PMID: 25799046
    6. The specific zone mutations in inhA gene for rifampicin and isoniazid were investigated with molecular methods in isolated unique PMID: 26506671
    7. Rational Modulation of the Induced-Fit Conformational Change for Slow-Onset Inhibition in Mycobacterium tuberculosis InhA. PMID: 26147157
    8. The study reports empirical parameters to differentiate the 'open' and 'closed' conformation of substrate-binding loop by comprehensive ana-lysis of InhA crystal structures. PMID: 24895891
    9. The results reveal that the presence of a mutation in the inhA regulatory region together with a mutation in the inhA coding region can lead to the development of high-level isoniazid resistance and cross-resistance to ethionamide among the MDR-TB strains circulating in Lisbon. PMID: 23539241
    10. No mutation was observed in the inhA promotor region or in the INH sensitive control isolate (H37Rv). PMID: 22358357
    11. We chose to search for new inhibitors of the enoyl-acyl carrier protein reductase InhA, the target of the first-line TB drug isoniazid. Two compounds (CD39 and CD117) were bactericidal against drug-susceptible and drug-resistant M. tuberculosis. PMID: 21628538
    12. inhA promoter mutations are strongly associated with extensively drug-resistant-tuberculosis in South Africa PMID: 21333101
    13. Phosphorylation of InhA inhibits mycolic acid biosynthesis and growth of Mycobacterium tuberculosis. PMID: 21143326
    14. InhA phosphorylation is an important event in regulating cell growth. PMID: 20864541
    15. inhA(S94A) allele confers clinically relevant levels of resistance to isoniazid killing & inhibition of mycolic acid synthesis. decreased binding of INH-NAD inhibitor to InhA establishes InhA as primary target of isoniazid action in M. tuberculosis. PMID: 16906155
    16. catalysis of substrate reduction by InhA results, in part, from correct orientation of the cofactor in the ground state PMID: 17472376
    17. T (-8)C of inhA mutations was found in multidrug resistant Mycobacterium tuberculosis isolates. PMID: 17539290
    18. The structure of two InhA mutants (I21V and S94A), identified in INH-resistant clinical isolates, were solved. PMID: 17588773
    19. inhibited by Anthecotulide from Anthemis auriculata PMID: 18424102

    顯示更多

    收起更多

  • 蛋白家族:
    Short-chain dehydrogenases/reductases (SDR) family, FabI subfamily
  • 數據庫鏈接:

    KEGG: mtu:Rv1484

    STRING: 83332.Rv1484



主站蜘蛛池模板: 纯爱无遮挡h肉动漫在线播放| 人人做人人爽久久久精品| 狠狠噜狠狠狠狠丁香五月| 精品久久久久香蕉网| 国产精品成人va在线观看| 亚洲欧美日本国产专区一区| 男女啪啪抽搐呻吟高潮动态图| 18禁超污无遮挡无码免费动态图| 国产精品老热丝在线观看| 真实国产乱子伦对白视频不卡| 亚色九九九全国免费视频| 亚洲精品第一区二区三区| 亚洲成a人片在线不卡一二三区 | 最近日本mv字幕免费高清完整版| 最近更新中文字幕免费大全| 日本精品人妻无码77777| 精品无码一区二区三区电影| 被c到高潮疯狂喷水国产| 国产末成年女av片一区二区| 最爽free性欧美人妖| 欧美成人免费全部观看国产| 亚洲成亚洲成网| 一本大道伊人av久久综合| 肥臀浪妇太爽了快点再快点| 在线亚洲综合欧美网站首页| 成 人影片 aⅴ毛片免费观看| 久久婷婷五月综合色中文字幕| 亚洲欧美中文日韩在线视频一| 国产精品麻豆aⅴ人妻| 欧美寡妇xxxx黑人猛交| 欧美 丝袜 自拍 制服 另类| 精品系列无码一区二区三区| 日韩精品 中文字幕 视频在线| 亚洲男人av香蕉爽爽爽爽| 国产在线精品无码二区| 草草网站影院白丝内射| 欧美老妇交乱视频在线观看| 久久精品国产福利一区二区| 国产v亚洲v天堂a无码99| 欧美巨大巨粗黑人性aaaaaa| 成人麻豆日韩在无码视频|