Team:HKUST/Protocols/PCR cleanup
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<li><a href="https://2009.igem.org/Team:HKUST/ToxinProduction">Toxin Production</a></li> | <li><a href="https://2009.igem.org/Team:HKUST/ToxinProduction">Toxin Production</a></li> | ||
Latest revision as of 09:55, 20 October 2009
a
PCR product clean-up
Purpose: To clean up primers, dNTPs, enzymes, short-failed PCR products in the PCR reaction.
Materials: FAPC Buffer,Wash Buffer, Elution Buffer, PCR Product (all provided in FavorPrepTM PCR Clean-Up Kit)Procedure:
a.Transfer 30μL of PCR product and add 5 volumes of FAPC buffer to a 1.5mL microcentrifuge tube, then mix well by vortexing.b.Place a FAPC Column into a Collection Tube and transfer the sample mixture to FAPC Column.
c.Centrifuge at 6,000 rpm for1 min then discard the flow-through.
d.Add 750 μl of Wash Buffer (ethanol added) to FAPC Column. Centrifuge at 6,000 rpm for 1 min, then discard the flow-through.
e.Centrifuge at 14,000 rpm for an additional 3 min to dry the column.
f.Place FAPC Column into an Elution Tube.
g.Add 40 μl of Elution Buffer or ddH2O (pH 7.0~8.5) to the membrane center of FAPC Column. Stand FAPC Column for 2 minutes.
h.Centrifuge at 14,000 rpm for 1 min to elute the DNA.
Tips:
In step f, for effective elution, make sure that the elution solution is dispensed onto the membrane center and is absorbed completely.- Agarose gel preparation and gel electrophoresis
- PCR (Taq, Vent)
- PCR product clean-up
- Enzyme digestion (vector, insert)
- Plasmid DNA extraction
- Gel cutting
- Gel extraction
- Ethanol precipitation
- Ligation
- Transformation to E.coli
- Transformation to yeast
- Cell lysis
- Yeast genomic DNA extraction
- Western blotting
- GFP testing