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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
常温
- 保质期:
根据瓶身LOT号查询
- 英文名:
D-(+)-Galactosamine hydrochloride
- 库存:
有现货
- 供应商:
浙江羽翔生物科技有限公司
- CAS号:
1772-03-8
- 规格:
10MG
属性
质量水平
200
方案
≥99% (HPLC)
表单
powder
技术
HPLC: suitable
杂质
≤0.5% Glucosamine (HPAE)
颜色
white to off-white
mp
172-180 °C
溶解性
H2O: 50 mg/mL, clear to slightly hazy, colorless to very faintly yellow
储存温度
room temp
SMILES字符串
Cl.N[C@@H](C=O)[C@@H](O)[C@@H](O)[C@H](O)CO
InChI
1S/C6H13NO5.ClH/c7-3(1-8)5(11)6(12)4(10)2-9;/h1,3-6,9-12H,2,7H2;1H/t3-,4+,5+,6-;/m0./s1
InChI key
CBOJBBMQJBVCMW-NQZVPSPJSA-N
一般描述
应用
- 甘露聚糖结合凝集素(MBL)与改性云母表面的表面结合
- 腹腔注射前的无菌磷酸盐缓冲液(PBS)中
- 小鼠中产生原发性骨髓来源的巨噬细胞(BMDM)
生化/生理作用
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文献和实验Saikosaponin a ameliorates lipopolysaccharide and d‑galactosamine-induced liver injury via activating LXRα.
Saikosaponin a (SSa), one of the major active components of Bupleurum falcatum, has antioxidant and anti-inflammatory pharmacological properties. However, the effects of SSa on liver injury have not been reported. In the present study, we evaluated the protective effects and mechanisms of SSa on lipopolysaccharide (LPS)/d‑galactosamine (D-GalN)-induced liver injury. The mice were pretreated with SSa 1 h before LPS/D-GalN treatment. The liver MPO, MDA, and the serum AST and ALT levels were tested by specific determination kits. The pro-inflammatory cytokines TNF-α and IL-1β were tested by ELISA kits. The expression of NF-κB signaling pathway and LXRα were tested by western blot analysis. The results showed that SSa significantly reduced the levels of liver MPO, MDA, and serum AST, ALT levels induced by LPS/D-GalN. SSa also dose-dependently inhibited LPS/D-GalN-induced pro-inflammatory cytokines TNF-α and IL-1β production. Furthermore, we found that SSa inhibited NF-κB signaling pathway activation induced by LPS/D-GalN. In addition, SSa dose-dependently increased the expression of LXRα. In conclusion, the results demonstrated that SSa had protective effect on liver injury and the anti-inflammatory mechanisms of SSa on LPS/D-GalN-induced liver injury may be due to its ability to increase LXRα expression. SSa might be a potential treatment for liver injury.
membrane,0.45um Millipore Acrylamide Amresco 0341 Bis-Acrylamide Amresco 0172 Glycine Sigma G8898 SDS Sigma L4390 APS Amresco 0486 TEMED Amresco 0761
这类药对中枢神经有较强烈的生理作用。有的可以使人在较短时间内呼呼入睡,通常叫做安眠药。有的能使人在短期内失去痛感,叫做镇痛药。还有一类能使中枢神经放松而后安定下来,叫做安定药。 (1)安眠药 安眠药一般在睡前半小时或15分钟服用。常用的是鲁米那、水合氯醛和安眠酮。鲁米那成人每次服0.03g,肌肉注射成人0.1g/次。水合氯醛口服成人每次1g。安眠酮成人每次0.1g。安眠药有一定的毒性,要在肝脏中解毒,肝病患者应慎服。特别是常服安眠药可以成瘾,以致累积中毒。服用安眠药醒
液D/10=Fml。 f. PBS量D-(B+F)=Gml。注:A为蛋白含量,mg/ml;B为蛋白质溶液的容积;C为蛋白总量,mg;D为常数,mg;正为荧光素的量,mg;F为碳酸盐缓冲液的容积,ml;G为PBS的容积,ml。③结合(或标记) 边搅拌边将称取的荧光色素渐渐加入球蛋白溶液中,避免将荧光素粘于烧瓶壁(大约在5—10min内加完),加完后,继续避光搅拌12h左右。结合期间应保持蛋白溶液于4℃左右,故需将烧杯和搅拌器一起移人4℃冰箱中。④透析 结合完毕后,将标记的球蛋白溶液离心(2500
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