Do you think the most accurate method is real-time pcr?
In which species you wish to amplify this gene?
Dear Sachinandan,
I'm working with my colleagues on psoriasis patients. We need to investigate the presence of mutations in this gene.
Hi,
if you are interested in variations (mutations) in that gene you have to do conventional PCR and Sanger sequencing. In the case that you want to search only one specific variation (mutation) you can design real-time PCR with specific probe.
Thanks for your answer.
Regards
Do not hesitate to contact me with further questions. Good luck.
Thanks again. I'm appreciated for you.
Nibras
It's very important question
Good question and useful answers
DNA visualization in the gel.
02 March 2017 8,755 8 View
I used DNA green dye as alternative to EthBr for the first time, the photos of the gel under U.V. light looks strange. this dye suppose to be green under blue light, but I have no idea about how...
02 March 2017 8,193 7 View
02 March 2017 7,071 5 View
Testing HLA matching for organ transplant with Luminex.
01 February 2017 2,210 4 View
I need to extract and purify extracellular proteins.
31 December 2016 2,211 4 View
I I need to know the method used for degasing of sephedix
31 December 2016 989 0 View
I need to know if running gel is essential after each step.
31 December 2016 2,257 4 View
Protocols for DNA extraction
31 December 2016 8,149 8 View
31 December 2016 2,246 2 View
I want to know if this works better than other products.
31 December 2016 3,739 2 View
Results of single-case research designs (i.e., n-of-1 trials) are often evaluated by visually inspecting the time-series graph and computing quantitative indices. A question our research team is...
03 March 2021 687 1 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 am going to have 3 different probes in my qPCR work that I am going to do. But I realized that the machine we have in the lab is a Rotor-Gene Q 2plex HRM Platform, saying it has green, yellow,...
01 March 2021 8,544 1 View
To dear Researchers, I was analyzing a series of concentration for estimation of Real-Time PCR efficiency. The concentration was 1:10. I used MS-excel to evaluate Slope. The result of slope was -8...
01 March 2021 8,683 4 View
Does anyone have the experience of using Taq Man probes in the QIAGEN Rotar- Gene qPCR machine?
01 March 2021 5,311 1 View
I am looking at the ATP1A2 (Sodium/Potassium ATPase alpha subunit 2) in two human neuronal cell lines. Expression levels of this protein seems to be almost equal when detected by one antibody....
01 March 2021 3,607 3 View
Is there any book chapter/book, webpage or research article available to understand genome-wide gene identification?
28 February 2021 8,095 1 View
Dear All, mirna primer showing some problem in the melting curve? any idea why? As attached is the melting curve. The forward sequence is obtained from miRBase and reverse primer is universal.
28 February 2021 5,008 4 View
I have two groups of brain samples, control and treated for example. It was total RNA nova seq sequencing. I tried all the available pipeline like: star+rsem+deseq2, Hista+stringtie+cuffdiff,...
27 February 2021 356 6 View
I performed site directed mutagenesis, transformation, and then I sent out plasmids for Sanger sequencing and found out that there is extension of DNA just before the stop codon. I am not sure...
27 February 2021 547 3 View