Changes

Jump to navigation Jump to search
added details
Line 42: Line 42:     
Measure DNA quantity/quality with Nanodrop.
 
Measure DNA quantity/quality with Nanodrop.
 +
 +
* yield was xxx - xxx ng/ul genomic DNA.
    
===PCR===
 
===PCR===
Line 48: Line 50:     
For 50 ul reaction:
 
For 50 ul reaction:
 +
 +
* xx ul Gotaq
 +
* xx ul mixture of 5 uM forward/reverse Tyro3 primers
 +
* xx ul dH<sub>2</sub>O
 +
* 1 ul of genomic DNA
 +
    
PCR: 95C for 1min, then 30 cycles of: 95C for 1min, 72C for 2min. (note annealing and extension steps combined into 2 min at 72C).
 
PCR: 95C for 1min, then 30 cycles of: 95C for 1min, 72C for 2min. (note annealing and extension steps combined into 2 min at 72C).
 +
       
===Gel===
 
===Gel===
   −
2% agarose in TAE (2 g agarose in 100 ml TAE, microwave 2 min at 50% power; add 10 ul of SYBR safe 10000x)
+
2% agarose in TAE (2 g agarose in 100 ml TAE, microwave 2 min at 50% power; add 10 ul of SYBR safe 10000x while cooling). Make mini-gel with 12-tooth comb
    
load 10 ul of 50bp ladder; 10 ul of PCR product + 2 ul purple loading dye
 
load 10 ul of 50bp ladder; 10 ul of PCR product + 2 ul purple loading dye
   −
run at 90V for 30 min
+
run at 90V for 30 min (or 65V for 60 min for sharper bands). Red dye front migrates at about 500bp [CHECK]
    
===PCR clean-up===
 
===PCR clean-up===
   −
[https://omegabiotek.com/product/pcr-clean-up-kit-e-z-n-a-cycle-pure/ E.Z.N.A. Cycle Pure Kit (V-spin)] yields 30 ul in dH<sub>2</sub>0
+
[https://omegabiotek.com/product/pcr-clean-up-kit-e-z-n-a-cycle-pure/ E.Z.N.A. Cycle Pure Kit (V-spin)] yields 30 ul in dH<sub>2</sub>O [ now trying kit elution buffer ]
 +
 
 +
Measure DNA quantity/quality with Nanodrop.
 +
 
 +
* yield was xxx - xxx ng/ul clean PCR product
 +
 
 +
===Re-Amplification===
 +
 
 +
To get higher concentration of DNA for digest, repeat PCR using 1 ul of clean PCR product and clean up.
 +
 
 +
* yield was xxx - xxx ng/ul clean re-amplified PCR product
 +
 
    
===Digestion===
 
===Digestion===
 +
 +
NEBiolabs says to mix digest with purple dye with 0.5% SDS to separate protein from DNA. SDS may interfere with SYBR Safe, so may need to post-stain the gel.

Navigation menu