11 Questions 19 Answers 0 Followers
Questions related from Nadia Jamil
I searched and it is not in https://beallslist.net/standalone-journals. I need guidance on it please.
02 July 2023 9,981 3 View
We are working on Dengue PCR and now after consistent good results we want to offer it on commercial level. But before that we would like to adopt an ISO standard. We have GLPs in place and for...
20 January 2022 8,617 0 View
Recently I read a paper (link is present below), where they mentioned that " Grain labs often remove impurities from samples before conducting a test. However, the purification of GMO samples is...
10 September 2018 769 0 View
Can we wash it by boiling it in water if the visible stains of ethidium bromide are not washed after rinsing with water and then 70% ethanol?
07 August 2018 8,155 3 View
If there is a number superscript on the sequence of a primer what does it means? e.g. T153AGCT etc
22 December 2017 4,905 1 View
I have seen following...
05 December 2017 8,162 3 View
I ran a PCR reaction and got my desired band at 800 bp with other non specific bands (reaction vol 25 ul) after optimization I got 800 bp band clear (reaction vol 25 ul). Then I went for bulk...
03 October 2017 3,985 7 View
I need enzymes that can work with my in-house PCR buffer. Please suggest if there is any good DNA polymerase and reverse transcriptase, I also do not have a lot of funds so I would be really...
03 October 2017 1,492 3 View
when we use reverse transcriptase do we have to use specific buffer with that or any taq buffer can also work with that?
03 October 2017 5,797 3 View
Hi there I isolated bacteria from serum sample did the extraction of DNA for bacteria, followed by PCR. PCR band was of 100bp I sent it for sequencing. The results were approx 43 bp forward primer...
04 August 2017 3,317 9 View
I need to Isolate bacterial DNA of high quality but without using kit.
30 March 2017 6,537 6 View