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Questions related from Michael Luke Ridley
Currently having trouble cloning some PCR cloned fragments (digested with NheI and XhoI) into a pGL4 vector. standard mix is 100ng of digested and TSAP treated vector and 3x molar amount of insert...
13 July 2017 2,867 1 View
To validate a microarray, we used SYBR green RT PCR for 25 genes. Just wondering what the best way to confirm whether those gene expression patterns were validated. We used 4 different treatments...
22 February 2013 7,670 1 View
