cDNA product separation
u8251012 at CC.KMC.EDU.TW
Sat Feb 1 14:46:44 EST 1997
1.my PCR product is 200, 240, 280 bp...
what GEL formula can I separate them clearly ?
2.My target mRNA is so few in quantity
Dose Northern blot analysis obtained better results if I purified
my mRNA by polyT-collum ?
3.DOSE DNase contaminate serious in labs ?
where did them usually exist ? , how can I get rid of that ?
Yang Yu-Lin: Kaohsiung medical College,Taiwan, ROC TEL:07-3121101 ext 2138
Lovely Biologist on Cellular Biochemistry :Major in Endocrynology and Signal
Working on : MAP kinase, PKC, PKA and cell cycle regulation in Kidney cells
E mail: u8251012 at cc.kmc.edu.tw
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