5' RACE
Revision as of 14:36, 4 December 2012 by Davebridges (Talk | contribs) (Rewrote protcol for first strand synthesis)
Revision as of 14:36, 4 December 2012 by Davebridges (Talk | contribs) (Rewrote protcol for first strand synthesis)
Materials
- 5' RACE Kit (Version 2.0 from Invitrogen; http://products.invitrogen.com/ivgn/product/18374058)
- Double distilled water
- Absolute ethanol
- Total RNA, 1-5 ug
- Gene Specific Primers (see Designing Primers for 5' RACE )
Protocol
Copied from the manufacturer's protcol here
Preparation
- Resuspend gene specific primers to 1 uM
- Prepare and chill wash buffer by adding 18 mL water, 21 mL ethanol and 1 mL wash buffer concentrate into a glass bottle. Place at 4C
- Prepare and chill 70% ethanol by adding 35 mL ethanol to 15 mL water in a glass bottle. Place at 4C
First Strand Synthesis
- Combine the following in a PCR tube:
- Incubate at 70C for 10 min to denature RNA using the PCR Program 5' RACE 70C
- Place on ice for 1 min
- Add the following in order:
- 2.5 uL 10X PCR Buffer
- 2.5 uL 25mM MgCl2
- 1 uL 10 mM dNTP
- 2.5 uL DTT
- Incubate 1 min at 42C using the PCR program 5' RACE First Strand, which covers the next three steps
- Add 1 uL SuperScript II RT
- Incubate 50 min at 42C
- Incubate 15min at 70C
- Remove and add 1uL RNAse H, mix thoroughly
- Incubate 30min at 37c using the PCR Program 5' RACE RNAse H. Can freeze at -20 or continue to cDNA Purification
Component | Amount |
---|---|
GSP1 | 2.5 pmoles (2.5 uL of 1 uM) |
RNA | 1-5 ug (from nanodrop) |
DEPC Water | To 15.5 uL |