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
Please contribute to this question with your assured knowledge. In treating cells for different time spans like 24h, 48h and 72h, should we seed different numbers of the cells suitable for...
04 December 2021 1,869 4 View
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 8,653 3 View
31 December 2018 9,062 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 8,474 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 3,227 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 5,656 7 View
31 December 2013 7,754 6 View
31 December 2013 3,015 8 View
Is there any useful remedy to use primer stock contaminated with DNA or cDNA?
06 July 2013 1,695 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 6,845 3 View
I would like to learn more about SPSS and Its application especially in regards to data analysis. Please suggest me how I can learn more about it. Thank you so much.
11 August 2024 9,101 4 View
I have reverse sequences (AB1 format), can I base on reverse DNA sequences to perform nucleotide alignment, convert nucleotides to amino acids and deposit the sequence in GenBank database?
11 August 2024 5,138 1 View
Hello, Why do i see this baseline drift when i compare my blank (black) to the sample (blue)? Any suggestions as to why this happened? Thank you!
11 August 2024 3,770 4 View
Willett, Shenoy et al. (2021) have developed a brain computer interface (BCI) that used neural signal collected from the hand area of the motor cortex (area M1) of a paralyzed patient. The...
10 August 2024 7,180 0 View
I'm currently exploring the application of Python in textile engineering, specifically in areas like data analysis, process automation, and the development of smart textiles. I'm interested in...
10 August 2024 7,429 2 View
How can I use the cif data obtained from rietveld refinement extracted via gsas2, for microstructural analysis using ETEX software?
09 August 2024 7,718 0 View
I'm cloning a fragment of 3200 nts into plasmid. The cloning was successful, however, 02 amino acids were mutated. Now I want to fix these 02 aa by site-directed mutagenesis technique using...
08 August 2024 4,645 2 View
After performing symmetric PCR, PCR purification was performed. Afterwards, asymmetric PCR was performed using the PCR purification product as a template, but no ssDNA band was confirmed in the...
08 August 2024 1,668 3 View
Let's say we have a standard, regular hexagonal honeycomb with a 3-arm primitive unit cell (something like the figure attached; the figure is only representative and not drawn to scale). The...
07 August 2024 1,937 1 View
A fungal strain was treated with nanoparticles. We want to do an environmental SEM analysis. So could anyone share your views on preparing the sample? Thank you.
07 August 2024 5,307 1 View