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Traditional method for lipid raft isolation involves cold non-ionic detergent extraction followed by sucrose gradient ultracentrifugation
Plant Golgi stacks are notoriously labile and loss of stack integrity can occur if harsh homogenization is used
MRTX1133 is a noncovalent
The entire protocol can be completed in less than 90 minutes
VC1kb DNA Ladder Pack Size:50 μg Traditional method for lipid raftServes as molecular weight standards for agarose gel electrophoresis. Suitable for sizing of PCR products or other double stranded DNA fragments. Fragments with size 2500bp are higher in intensity in comparison to other bands to serve as orientation points.