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S80090

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上海源葉生物科技有限公司是一家專門從事生物技術(shù)相關(guān)產(chǎn)品研發(fā)和銷售的綜合性生命科學(xué)公司,在全體員工的不懈努力和廣大客戶的大力支持下,公司迅速成長為一家擁有生物試劑部、實驗及醫(yī)用耗材部、生命科學(xué)儀器部以及技術(shù)服務(wù)部等部門的高新技術(shù)企業(yè)。





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  • 提示:詳情請下載說明書。
  • 產(chǎn)品描述: Tacrolimus monohydrate (FK506 monohydrate), a macrocyclic lactone, binds to FK506 binding protein (FKBP) to form a complex and inhibits calcineurin phosphatase, which inhibits T-lymphocyte signal transduction and IL-2 transcription. Immunosuppressive properties
  • 靶點: Macrolide
  • 體內(nèi)研究: The therapeutic effect of Tacrolimus is investigated on progression and perpetuation of colitis by administering Tacrolimus to Dextran sulfate sodium (DSS)-treated mice from Days 10 to 16 or to 23. At Days 17 and 24, colon length is significantly shortened, and colon weight is significantly higher in DSS-treated control animals than in normal animals. In addition, colon weight per unit length in the control group is more than twice that in the normal group. While both 7 and 14 d treatment with Tacrolimus significantly suppresses increases in colon weight per unit length in DSS-treated animals compared with the control group, this treatment does not actually restore the colon shortening. In addition, this inhibitory effect of Tacrolimus on increases in colon weight per unit length is more pronounced with 14-d than 7-d treatment, as shown by the inhibitory percentages (59% vs. 28%)
  • 參考文獻(xiàn):
    1. Thomson AW, et al. Mode of action of Tacrolimus (FK506): molecular and cellular mechanisms. Ther Drug Monit. 1995 Dec;17(6):584-91. 2. Okada Y, et al. Tacrolimus ameliorates dextran sulfate sodium-induced colitis in mice: implication of interferon-γ and interleukin-1β suppression. Biol Pharm Bull. 2011;34(12):1823-7. 3. Vogel KR, et al. mTOR inhibitors rescue premature lethality and attenuate dysregulation of GABAergic/glutamatergic transcription in murine succinate semialdehyde dehydrogenase deficiency (SSADHD), a disorder of GABA metabolism. J Inherit Metab Dis. 2016 Nov;39(6):877-886. 4. Zhu H, et al. Tacrolimus promotes hepatocellular carcinoma and enhances CXCR4/SDF 1α expression in vivo. Mol Med Rep. 2014 Aug;10(2):585-92.
  • 溶解度: DMSO  :  100  mg/mL  (121.65  mM;  Need  ultrasonic)    H2O  :  <  0.1  mg l  (ultrasonic;warming;heat  to  60°c)  (insoluble)="">
  • 保存條件: -20℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 1.217 ml 6.083 ml 12.165 ml
    5 mM 0.243 ml 1.217 ml 2.433 ml
    10 mM 0.122 ml 0.608 ml 1.217 ml
    50 mM 0.024 ml 0.122 ml 0.243 ml
  • 注意:部分產(chǎn)品我司僅能提供部分信息,我司不保證所提供信息的性,僅供客戶參考交流研究之用。


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