Tianjin/FLIP-FLOP/More details

Solid LB culture is used for agar plate. For a typical liquid culture, use 5 ml or 100ml of appropriate medium, and condition is supposed to be 37°C and 220rpm.. The amount of time you wait depends on the reason for growing the cells. To miniprep plasmid DNA, an overnight culture is sufficient. To get the transformation colony, wait about 12-16 hours.

Using plasmid extracting kit we get the plasmid DNA for two purposes. One is verifying the plasmid using enzyme digesting and the other is purifying the fragment using enzyme digesting and agarose gel electrophoresis.

Colony PCR can be used after a transformation to screen colonies for the desired plasmid.But it always give the incorrect result, so often we use enzyme digesting to verify the desired palsmid.

10μL digesting Mix

50μL digesting Mix

The fragment usually is gotten from gel purification, sometimes from nucleic acid co-depositing.
Reagents

Calculating
The amount of vector and insert fragment is decided by formula given by openwetware.

Reaction
Ligate reaction is taken by TaKaRa DNA Ligation Kit Ver.2.0. Total volume is 10μL, one half is DNA solution and one half is Solution I. Temperature is 16°C. Then waiting for different time according to different situations.

Using CaCl2 solution to make competent cells, and chemically transform foreign DNA to competent cells. If foreign DNA is plasmid, using 2-3 μL to transform 100 μL competent cells. If it is ligation product, transform the total 10 μL jproduct to 100 μL competent cells.

Open the bottle of medium and flame the mouth, measure out 2 ml to fill 10 ml Eppendorf Tube.Centrifugate the tube and pipette in 5 ml of the suspension to another tube for detecting the extracellular AHL.Then the deposit is used to detect GFP using fluorometry. AHL is detected by the detector used in Bio-Diode.