
The fundamental structure of cell membranes is bilayers composed of phospholipids, and the vital function of the phospholipids in the membrane is to help keep it fluid and semi-permeable. Conventional glycerophospholipids have acyl chains attached to the sn-1 and sn-2 positions of the glycerol backbone via an ester bond. Ether lipids are a unique class of glycerophospholipids that have an alkyl chain attached to the sn-1 position by an ether bond (glycerol-ether lipids). In ether lipids, the alcohol group attached to the phosphate is generally choline or ethanolamine. Ether-linked phospholipids such as 1-alkyl-2-acyl-phosphatidylcholine and dialkylphosphatidylcholine are also found in the plasma and organelle membranes of mammalian species. Ether lipids form approximately 20% of the total phospholipid in mammals with different tissue distribution; brain, heart, spleen and white blood cells have the highest levels, while liver have a very little amount of ether lipids.
Studies on the formation and thermodynamic properties of ether-linked phospholipid bilayer membranes have indicated that in contrast to ester-linked phospholipid, the formation of the non-bilayer structure takes place spontaneously. This is attributed to the weaker interaction between polar headgroups in the ether-linked than that in the ester-linked phospholipids. It has also shown that the phase behavior of the ether-linked phospholipid bilayer membranes in ambient pressure is almost equivalent to that of the ester-linked phospholipid bilayer membranes under high temperatures and pressures, and the difference in the phase behavior decrease as the alkyl-chain length increases.
Due to distinctive properties of ether lipids, liposomes made from ether lipids exhibit very unique characteristics and performance: a) the ether bonds are more stable than ester linkages over a wide range of acidic or alkaline pH; b) stability properties of the liposomes is enhanced by bipolar lipids, and the saturated alkyl chains gives stability towards degradation in oxidative conditions; c) the unusual stereochemistry of the glycerol backbone enhance the resistance against the attacks by other organism phospholipases.
Phospholipase A2 (PLA2) cannot hydrolyze the ether lipid liposomes. Diether lipids do not go through hydrolysis due to having an ether bond instead of an acyl bond and therefore to do that, they are a suitable candidate for experiments that needs to be performed at a higher temperature for an extended period of time. For more information about hydrolysis and oxidation of phospholipids see here.


Saturated diether lipids can neither be hydrolyzed nor oxidized.

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1.模板提取(一般为RNA):Trizol、氯仿、异丙醇、无水乙醇、DEPC处理水
2.模板浓度测定:分光光度计或NanoDrop
3.逆转录:逆转录试剂盒(或者一步法试剂盒),这一步可以用普通PCR做,也可以用水域做。
4.荧光定量PCR试剂:通常有用SYBR Green Mix做的,但是这里建议你用EvaGreen做,灵敏度和平行性都要好于SYBR Green,并且如果你那是ABI或者Stratagene的PCR如果用SYBR Green还需要加一步Rox很麻烦。
5.其他:除了以上的那些还需要离心管、PCR管或板(Axygen反应比较好)、移液枪等,暂时就想到这么多。
定性ELISA只能粗略表示样本待测物含量在某个特定值以上或以下,定性ELISA通常设置阳性对照(P)、和阴性对照(N),结果分别用“阴性”和“阳性”表示。ELISA定性测定的“阴性”和“阳性”的判断标准是试剂盒所确定的阳性判断值,即cut-off值。
定量ELISA是通过一系列不同已知浓度的标准品所对应的OD值做出标准曲线,然后将样本的OD值代入标准曲线,计算出样本中待测物的含量。百特纯大分子Meretciel的定量ELISA试剂盒还可以。
谢谢谢
1.模板提取(一般为RNA):Trizol、氯仿、异丙醇、无水乙醇、DEPC处理水
2.模板浓度测定:分光光度计或NanoDrop
3.逆转录:逆转录试剂盒(或者一步法试剂盒),这一步可以用普通PCR做,也可以用水域做。
4.荧光定量PCR试剂:通常有用SYBR Green Mix做的,但是这里建议你用EvaGreen做,灵敏度和平行性都要好于SYBR Green,并且如果你那是ABI或者Stratagene的PCR如果用SYBR Green还需要加一步Rox很麻烦。
5.其他:除了以上的那些还需要离心管、PCR管或板(Axygen反应比较好)、移液枪等,暂时就想到这么多。
MicroBCA试剂测定范围是0.5-20μg/ml
楼主自己看看经销商价格