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- 详细信息
- 文献和实验
- 技术资料
- 库存:
57
- 英文名:
Fluphenazine dihydrochloride
- CAS号:
146-56-5
- 供应商:
上海莼试
- 保存条件:
Store at RT
- 规格:
100mg 500mg
1.本蛋白酶抑制剂混合物为100×的储存液,使用时按照1:100的比例加入到裂解液中(例如,1ml裂解液中加入10μl蛋白酶抑制剂混合物),混匀后即可使用。根据需要,0.5M的EDTA也按照1:100的比例加入到裂解液中(如用于检测金属蛋白酶活性,则不宜添加EDTA)。含有蛋白酶抑制剂混合物的裂解液宜现用现配,不宜配制后冻存待后续使用。
2. 待所需的抑制剂添加完毕混匀后,就可以开始进行哺乳动物组织的裂解和蛋白提取。
商品属性:
| 货号 | CS-01Y76782 | 规格 | 100mg 500mg |
| CAS号 | 146-56-5 | 分子量 | 510.44 |
| 含量 | >99.00% | 别名 | N/A |
| 分子式 | C22H28Cl2F3N3OS | 化学名 | 2-(4-(3-(2-(trifluoromethyl)-10H-phenothiazin-10-yl)propyl)piperazin-1-yl)ethanol dihydrochloride |
| 产地 | 国产 | 用途 | 仅供科研研究实验 |
分子式:C22H28Cl2F3N3OS
分子量:510.44
溶解度:DMF: 30 mg/ml,DMSO: 20 mg/ml,Ethanol: 5 mg/ml
储存条件:Store at RT
General tips:For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.
Shipping Condition:Evaluation sample solution : ship with blue ice All other available size: ship with RT , or blue ice upon request
EC50: 1.24 μMFluphenazine is a dopamine D1 and D2 receptor inhibitor.Dopamine D1 and D2 receptor immunohistochemistry has been used to study the structure of the adult rat arcuate-median eminence complex, particularly in relation to the tubero-infundibular dopamine neurons.In vitro: Previous study showed that both phenothiazines of fluphenazine and perphenazine induced concentration-dependent loss in cell viability with EC50s to be 1.24 and 2.76 μM for fluphenazine and perphenazine, respectively. Moreover, fluphenazine at 1.0 μM and perphenazine at 1.0 and 3.0 μM could inhibit melanogenesis and decrease the content of microphthalmia-associated transcription factor. In addition, both fluphenazine and perphenazine at higher concentrations caused depletion of melanocytes antioxidant status, indicating oxidative stress induction [1].In vivo: Systemic fluphenazine could effectively attenuate mechanical allodynia in rat neuropathic pain models at 0.03-0.3 mg/kg doses, which approximated those used in rodent models of psychosis. For antiallodynic effect, fluphenazine was able to effectively suppress the ectopic discharges in injured afferent fibers without affecting the propagation of action potentials in an ex-vivo DRG-nerve preparation from CCI rats [2].Clinical trial: Fluphenazine, which is sold under the brand names Prolixin, is clinically used as an antipsychotic medication in the treatment of chronic psychoses such as schizophrenia. In addition, fluphenazine is about equal in effectiveness to low-potency antipsychotics
注意事项:
抗逆滴加序列
每次向板内滴加抗原时,移液器滴头要与平面45度悬空,不要触碰到孔内的液体,由后向前依次滴加(即浓度由低往高滴加)。
抗感染反应期
抗原抗体在室温20~25℃下,必须反应30min以上,若环境温度低于室温,可将微量反应板置于恒温培养箱中,使二者充分反应。
旅游温度
磷酸盐缓冲液的pH值要在高压灭菌后进行滴定,往往在高压后pH值会有所改变,所以高压后再调一次pH值更为准确。磷酸盐缓冲液一经使用保存期不要超过3周。当pH<5.8时,红细胞会产生自凝现象;当pH>7.8时,图形洗脱加快,易造成肉眼观察产生误差;p H=7.2时,红细胞沉降最充分,图形最清晰。
当滴注 1%红细胞悬液时,应经常摇晃红细胞悬液,使红细胞均匀地分布在磷酸缓冲液中,以防止红细胞下降。
反应时间及温度
加入鸡红血球之后,反应板在室温(20~25℃)静置30~40min,对照孔血球下沉于孔底,即可判定结果。若室温达不到实验要求,需相应调整反应时间。当环境温度低于4℃时,红细胞发生自凝;高于37℃时,会发生反应物分离和红细胞溶血。
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文献和实验mg/日,分2次肌内注射。 盐酸三氟拉嗪(trifluperazine hydrochloride)10~30mg/次,分3次服。 盐酸氟奋乃静(fluphenazine hydrochloride)2~20mg/日。 氟奋乃静癸酸酯(fluphenazine decanoate)每2周25mg,肌内注射。 氟普噻吨(chlorprothixene)轻症150mg/日,重症300~600mg/日,口服。 氟哌啶醇(haloperidol)口服2~10mg/次
疟原虫 Malaria Parasites(Plasmodium)
can be used:Quinine dihydrochloride 20 mg salt/kg base given I.V. in 5% w/v dextrose or normal saline as a once-only 4 hour infusion followed, 4 hours later, by quinine dihydrochloride 10 mg salt/kg base 4-hour infusions 8 hourly.Where a syringe pump
酸三氟拉嗪(trifluperazine hydrochloride)10~30mg/次,分3次服。 盐酸氟奋乃静(fluphenazine hydrochloride)2~20mg/日。 氟奋乃静癸酸酯(fluphenazine decanoate)每2周25mg,肌内注射。 氟普噻吨(chlorprothixene)轻症150mg/日,重症300~600mg/日,口服。 氟哌啶醇(haloperidol)口服2~10mg/次,3次/日,肌内注射,5mg/次。
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