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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
−20°C
- 保质期:
根据瓶身LOT号查询
- 英文名:
Cardiolipin sodium salt from bovine heart
- 库存:
有现货
- 供应商:
浙江羽翔生物科技有限公司
- CAS号:
见瓶身
- 规格:
10MG
属性
生物来源
bovine heart
质量水平
200
方案
≥97% (TLC)
表单
lyophilized powder
脂质类型
phosphoglycerides
运输
ambient
储存温度
−20°C
一般描述
应用
- 作为薄层色谱法定量分析粗糙脉孢菌总线粒体脂质的磷脂标准品(89)
- 作为反相高效液相色谱(RP-HPLC)定量分析细菌脂质提取物的内部标准品(90)
- 作为抗原用于评估系统性红斑狼疮(SLE)患者的IgM反应(91)
生化/生理作用
包装
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文献和实验Cardiolipin content, linoleic acid composition, and tafazzin expression in response to skeletal muscle overload and unload stimuli.
Cardiolipin (CL) is a unique mitochondrial phospholipid that, in skeletal muscle, is enriched with linoleic acid (18:2n6). Together, CL content and CL 18:2n6 composition are critical determinants of mitochondrial function. Skeletal muscle is comprised of slow and fast fibers that have high and low mitochondrial content, respectively. In response to overloading and unloading stimuli, these muscles undergo a fast-to-slow oxidative fiber type shift and a slow-to-fast glycolytic fiber type shift, respectively, with a concomitant change in mitochondrial content. Here, we examined changes in CL content and CL 18:2n6 composition under these conditions along with tafazzin (Taz) protein, which is a transacylase enzyme that generates CL lipids enriched with 18:2n6. Our results show that CL content, CL 18:2n6 composition, and Taz protein content increased with an overload stimulus in plantaris. Conversely, CL content and CL 18:2n6 composition was reduced with an unloaded stimulus in soleus. Interestingly, Taz protein was increased in the unloaded soleus, suggesting that Taz may provide some form of compensation for decreased CL content and CL 18:2n6 composition. Together, this study highlights the dynamic nature of CL and Taz in skeletal muscle, and future studies will examine the physiological significance behind the changes in CL content, CL 18:2n6 and Taz.
一、实验部分 1.仪器及试剂 超纯水(Milli Q超纯水系统纯化),牛血清白蛋白(BSA)、异硫氰基荧光素(FITC)(美国Sigma-Aldrich公司),漩涡混合器(德国IKA公司),移液器(10μL、20μL、100μL、200μL、1000μL,法国Gilson公司),十六烷基三甲基溴化铵(CTAB,美国Fluka公司)、氯化钠(北京鼎国生物技术有限公司)、Tris、EDTA二钠盐(Invitrogen 公司),分析天平UMX2(0.1g感量,瑞士Mettler
把鲑鱼精子DNA(Sigma,Ⅲ,盐钠)溶解于水配制成10mg/ml的浓度,必要时于室温磁力搅拌2~4h助溶。把溶液中NaCl的浓度调至0.1mol/L,并用酚和酚/氯仿各抽提一次,回收水相。合DNA溶液快速通17号皮下注射针头12次,以剪切DNA。加入2倍体积用冰预冷的乙醇沉淀DNA。离心回收DNA并重溶于水,配制成10mg/ml的浓度,测定溶液的OD260值并计算出精确的DNA浓度,然后煮沸10min,分装成小份保存于-20℃。使用前置沸水浴中加热5min,然后迅速在冰浴中骤冷。预杂交液中应含有
253 1.37×104 C 271 9.10×103 T 260 7.40×103 比色杯光径为1cm时,吸光度=εM 13.0.5mol/l EDTA(pH8.0)溶液 【配制方法】 在800ml水中加入186.1g二水乙二胺四乙酸二钠(EDTA-Na•2H2O),在磁力搅拌器上剧烈搅拌,用NaOH调节 溶液的pH值至8.0(约需20g NaOH颗粒)然后定容至1L,分装后高压灭菌备用。 【注意】 EDTA二钠盐
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