Basically when coating particles we need to pay careful attention to:
- pH: This is most important!
- Timing of incubation
- Temperature of incubation
- Salt concentration
- Size of particles
- Freshness of Spermidine (0.1M)
- 2.5 M CaCl2 is filter sterilized and aliquots prepared ready to use.
- Purity and concentration of DNA
- Keeping particles suspended in the buffer solution while adding the spermidine and CaCL2
- We have seen problems with particles sticking to the 1.5 Ml centrifuge tubes. DNA Lo-Bind tubes should work better.
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