This is the best set up for the primer I have for miRNA I am working with. This curve happens for all my samples. I myself think it is not applicable. I need your comments. Thank you all.
https://arashazimzadeh.shutterfly.com/
Try to run your products on the gel. If you get one specific band for all of your samples, then I guess your melting curves are ok.
I think you have a second product indicated by the curve at the lower temperature.. Can be primerdimers.. As Irina suggested run a agarose gel
Dear researchers; A question arose for me about Real-Time analysis. I would appreciate you to comment about the question. For expression analysis we need a housekeeping gene to normalize Ct...
27 January 2019 8,561 3 View
31 December 2018 8,979 4 View
I'm going to study the expression of a particular micro-RNA in tumor samples in comparison to normal tissue. We obtain gastric tumor and normal samples from same patient. How many samples do we...
03 April 2015 8,370 3 View
Dear friends, The picture in the link below shows Melt Curve for the primer I have for the miRNA I am working with. This is the best set up that can accur for all 40 cDNAs. I myself think it is...
12 January 2014 3,150 6 View
This is the best set up for the primer I have for the miRNA I am working with. It is same for all 40 samples. I myself think it is not applicable but, I need your comments. Thank you all.
11 January 2014 5,575 7 View
31 December 2013 2,949 8 View
31 December 2013 7,694 6 View
Is there any useful remedy to use primer stock contaminated with DNA or cDNA?
06 July 2013 1,637 17 View
I'm doing my my thesis on miRNA differential expression. A question arose when preparing for standard curve, should cDNA or its PCR product be used? When can we use each of them? Another question...
14 June 2013 6,789 3 View
05 June 2013 6,754 3 View
Hiiiii everyone! I have an enquiry on statistical analysis. I was looking for many forum and it's still cannot solve my problem. I want to compare means of two groups of data but only with two...
03 March 2021 8,796 3 View
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
03 March 2021 3,568 1 View
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...
03 March 2021 5,978 5 View
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...
03 March 2021 1,401 3 View
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...
03 March 2021 8,920 3 View
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...
03 March 2021 6,994 5 View
I have a dataset with about 80 different species. As usual, some species are very easy to identify with certainty whereas others are more difficult, which means that I am less certain of my...
03 March 2021 8,066 4 View
Hello, We would like to increase the yield of our PCR product. We are running a series of PCR reactions that is targeting ~1.1kb sequence. We begin each reaction with ~400pg of template DNA...
02 March 2021 4,029 3 View
I just wanted to check if I need to run a linear regression separately if I am using PROCESS MACRO to run mediation analysis. Thank you.
02 March 2021 4,359 3 View
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
02 March 2021 7,670 3 View