Hello Researches,
I want to preserve my petri dish with her bacteria for a long time and harding the phenotype. Like in the symposium microbia.
So plzzz any recommendations?
I am currently writing my dissertation on the potential effect of bilingualism on intelligence scores. The latter is represented by a scale on the Y axe. My independent variable is the linguistic...
24 January 2021 5,336 2 View
I have data of received power (traces of 5000 samples)where the large scale fading and small scale fading are mixed. My goal is to analyze the small scale fading. For this reason, I have averaged...
13 February 2020 998 2 View
I have M traces containing values of the received power. The duration of the trace is 5 seconds and contains 5000 samples. I want to do a statistical analysis of the small scale fading of this...
11 February 2020 8,431 3 View
I am facing difficulties in cloning a 1kb gene into a vector (pJIT163). I have my gene on interest (GOI) in pUC57 and want to clone in pJIT163 using SalI and BamHI restriction sites. I am getting...
25 February 2021 3,221 7 View
Hello, I am currently using a Cas9 knock in system that will be expressed in the liver. To do so STOP codon fl/fl Cas9 KI mice were bred with Albumin-Cre mice to generate heterozgous pups, that...
24 February 2021 5,759 3 View
We have thin roots of from 1 year old different species of plants. We are looking into anatomical details of the roots. What's the best method to preserve and process the roots once they are...
23 February 2021 1,898 1 View
I am working on C6 cells along with other neuronal cell lines. We have preserved the cells in 90%FBS and 10% DMSO solution. We are reviving the cells after a year and cells are either not binding...
18 February 2021 4,499 1 View
Hi, I am stuck with a cloning experiment: The insert & backbone(bb) share one compatible end at 3' end(NotI) and one incompatible end at 5' end (XbaI for insert; HindIII for backbone). So i...
16 February 2021 1,664 3 View
Hello. I am currently trying to express a recombinant gene with Avitag at the N-terminal. I'm aiming at a final product that looks like this: Avitag-(target protein) The protein I use is already...
14 February 2021 2,039 4 View
03 February 2021 1,111 5 View
Hello I am infecting cells with bacteria in a well and then I am doing serial dilution of this well 1 in 10 and culture the two last dilution on MHA agar I have difficulty in getting accurate...
26 January 2021 9,256 5 View
I acquired the plasmid in Addgene, reconstituted the filter paper where the plasmid comes from with 30 microliters of TE buffer pH 8, immediately afterwards perform the transformation of E.coli...
25 January 2021 2,526 3 View
I have tried to use TTC agar overlay method for a few times to identify respiratory-deficient yeast which were affected by EthBr. The problem is that cells which should have stayed white also have...
22 January 2021 585 10 View