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Questions related from Amine Bouchareb
I'm performing a knock out of a gene in Zebrafish using CRISPR. But i have a problem with ligation. I cannot ligate my insert in the BsaI digested DR274! Protocole used: -Digest backbone DR274:...
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I'm performing rt-PCR on microRNA, in some reactions I have an efficiency >100 (200%) and in others it's < 100 (65%), I'm working with fast sybrgreen (applied biosystem), cDNA (1/100), primers...
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If possible, please give me some information about efficiency and position for the cleavage site (TALEN or CRISPR). Thank you for your answers.
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Hi, I'm setting up an experiment where I need to genotype different mouse samples using amplicon sequencing and I'm planning to not use any kit for my library prep. Adapting the 16S Metagenomic...
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