I have tried various different protocols for reverse transcription with random primers and I don't see any obvious difference in the final qPCR reaction. Any suggestions?
I would also like to know if DTT is needed if we use Rnasin and not rnasOUT.
So i finally have answer from promega dtt is not needed for rnasin working
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I have a problem with the logic of an RNA IP normalization. I am comparing two RNA binding proteins tagged with GFP, one is an isoform of the other where I mutated one binding site. My IP is done...
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If it is the case is it a problem for qrtPCR after that as I do reverse transcription with a random hexamer. Thanks for your answer.
31 December 2013 4,814 4 View
I wanted to know if it is a problem to precipitate RNA in isopropanol at 13000g because in a lot of protocol says to precipitate at 12000g.
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I am on the lookout for the Enhanced Yellow Fluorescent Protein (Aequorea victoria) DNA sequence. Does anyone know where I can find it? Thank you in advance
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Hi, I want to start testing pitfall trap to obtain ants samples, but I need to conduct molecular analysis on those insects. So, what kind of fluid can I use? Ethanol expires too early and I need...
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What's the best way to measure growth rates in House sparrow chicks from day 2 to day 10? Since, the growth curve from day 2 to 10 won't be like the "Logistic curve" it might not follow logistic...
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I have conducted and published a systematic review and meta-analysis research with the topic related to public health and health pomotion (protocol was registed in PROSPERO). Now we want to...
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dear community, my model is based feature extraction from non stationary signals using discrete Wavelet Transform and then using statistical features then machine learning classifiers in order to...
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Gel electrophoresis, RNA degradation, RNA extraction from fresh tissue
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If the detection range is in ng/ml but the reference range is in ug/ml for a molecule or protein in serum or plasma .how to dilute and what is the initial volume to be taken for quantitative analysis
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