How to calculate the number of bacterial colonies by culturing dilutions on the plate?
3 dilutions: more than300 (10^-1, 10^-2, 10^-3)
2 dilution: 30-300 (10^-4,10^-5)
1 dilution: 0 (10^-6)
Is the chitosan solution soluble in the physiological environment of PBS (pH: 6.2)?
27 December 2020 1,263 3 View
a transport model (e.g logit model or ...) is based on statistical data and field works or merely based on mathematical theories or both of them? If I want to define a model ( e.g. a new model in...
19 May 2020 1,768 3 View
How can I get the Sigma Plot software training file?
03 May 2020 5,549 5 View
I did acid etching on teeth with HCL 15 % .then analyzed with BET to fined porosity size. can anybody help me with an interpretation of BET analysis of bulk teeth? I want to know if I can...
09 January 2020 6,735 2 View
Hi, I made 40% urea broth medium(Biolife Italiana) to find out the presece of helicobacter pylori in gastric biopsy but this medium responds very slowly for positive biopsy (about 2 hours) while...
07 February 2019 6,804 7 View
Hi, In my problem, I have defined 2 domains; solid domain (spheres) and fluid domain (the space between them). In sub domain I have defined heat source but I have a problem with its unit! I...
05 August 2018 9,824 5 View
Hi colleagues, I am working on digitization of insects. I would like to use the latest hardware and software which can produce 3D image and maintains the natural colour of the specimen. Kindly...
08 March 2018 3,018 4 View
What is the best method, condition, and strain of E. coli that can be used during transport and storage of large size plasmids "27~35 kbp. Although, I was able successfully transport the target...
05 December 2017 5,775 3 View
I am currently working on a project using ANSYS workbench but finding it very difficult to run large simulations on my laptop. I was wondering if anyone has any experience on how to prepare the...
09 May 2017 2,341 1 View
29 October 2016 2,119 1 View
After I cryofreeze the cell do I need to remove the DMSO for culturing the cell for next passages .
28 February 2021 7,738 3 View
I want to use 0.1% gelatin. Should that be made in PBS or sterile water? Should I autoclave the gelatin soln after making it in water/PBS?
28 February 2021 274 2 View
Hello, I am looking for some expertise on culturing MCF7s. I purchased them from ATCC and I have been following all media and culture conditions. Media is EMEM with 10% FBS and 10ug/mL of...
27 February 2021 3,904 2 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
I've been having a hard time forming an endothelial monolayer with good tight junctions. The person who trained me on the culture of endothelial cells worked mostly with mouse BMEC, and he used...
22 February 2021 8,253 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
Hi there! My lab has been brought an array of C-4 I cell line. The cells did not succeed in attaching to the bottom of the flask and remained floating in the media. Although we followed the...
04 February 2021 10,018 5 View
03 February 2021 1,111 5 View