User:Cassandra M Barrett/Notebook/Haynes Lab/2015/08/24: Difference between revisions
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== | ==GoTaq PCR for T2A-EGFP and mtCas Fragments== | ||
Purpose: To amplify fragments via PCR for two side projects. T2A-EGFP fragment is being amplified for Dr. Haynes. Other two fragments are being amplified for Rene's mtCas project from Cold Spring Harbor. | Purpose: To amplify fragments via PCR for two side projects. T2A-EGFP fragment is being amplified for Dr. Haynes. Other two fragments are being amplified for Rene's mtCas project from Cold Spring Harbor. | ||
Revision as of 11:00, 4 September 2015
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GoTaq PCR for T2A-EGFP and mtCas FragmentsPurpose: To amplify fragments via PCR for two side projects. T2A-EGFP fragment is being amplified for Dr. Haynes. Other two fragments are being amplified for Rene's mtCas project from Cold Spring Harbor. Methods (T2A-EGFP): Amplifying fragment from pX330g reattempt, using GoTaq this time Set up reaction with P231 and P232 GoTaq MM 25uL Template (undiluted) 1uL FP 2.5uL RP 2.5uL Water 19uL Run on GoTaq PCR protocol (60C, 30sec) Results: Band on gel around 850bp as desired, product cleaned up with Qiagen PCR clean up kit Methods (mtCas): Amplifying two different fragments for mtCas experiment Using P259/260 and P261/262 GoTaq MM 25uL Template 1uL FP 2.5uL RP 2.5uL Water 19uL Run on GoTaq PCR protocl (60C, 90sec) Results: Band on gel for fragment amplified with P259/260 primer set but not for other one. First fragment cleaned up using Qiagen PCR clean up kit
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