Ob/ob Genotyping
Revision as of 19:59, 26 September 2013 by Davebridges (Talk | contribs) (added nots on how to make primer mixes and added band sizes)
Revision as of 19:59, 26 September 2013 by Davebridges (Talk | contribs) (added nots on how to make primer mixes and added band sizes)
Used method described in Ellet et al (http://dx.doi.org/10.1038/oby.2008.443)
Primers
- ob/ob RFLP-F: 5'- TGA GTT TGT CCA AGA TGG ACC -3'
- ob/ob RFLP-R: 5'- GCC ATC CAG GCT CTC TGG -3'
- ob/ob - WT-Lep-F: 5'- AAT GAC CTG GAG AAT CTC C -3'
- ob/ob - Lepob-R: 5'- GCA GAT GGA GGA GGT CTC A -3'
Primer Mixes
Primers are resuspended at 100 uM, so add 3x10 uL of the primers to 970uL of water to make the primer mixes:
- For WT Primers combine both RFLP primers with the WT-Lep-F primer
- For Ob Primers combine both RFLP primers with the Lebob-R primer
PCR Reaction
The PCR program is called ob-ob and is:
- 95 °C 2 min
- 40 cycles of:
- 95 °C 30 s
- 58 °C 30 s
- 72 °C 45 s
- 72 °C 7 min
Bands
There should be a control band in all lanes at 191bp For the wt primers if there is one or more wt alleles there should be a band at 104bp For the ob primers, if there is one or more ob alleles there should be a band at 123bp