I want to seed normal endometrial cells
It differs for various cell lines. You need have pre-experiments by using different concentrations to find optimized seeding number. Usually, each dish needs 500000-2000000 cells.
I am using the Inoue buffer for the preparation of competent cells. Can it be used after storage on 4 degrees? The references recommend the usage of freezed aliquots or fresh buffer every time.
02 March 2019 9,745 1 View
09 October 2016 6,955 8 View
Does using EDTA antigen retrieval buffer in immunohistochemistry gives high background stains and citrate buffer gives low background stain?
01 February 2016 158 1 View
I extracted DNA using extraction column. It appeared that there was a lot of cell debris in the extract. Lot of impurities appeared in the nanodrop specking. How can I remove the cellular debris...
06 July 2015 2,139 8 View
I would like to culture endometrial cells to confluence into culture dishes. I would like to know if anyone has a good protocol with the mention of the need of coated dishes or other special...
04 May 2015 935 4 View
I am expressing a protein tyrosine kinase in mammalian cells. Is it necessary to incorporate a Kozak sequence before the ATG initiation codon to assure that the expression happens? My sequence...
04 May 2015 6,743 17 View
02 March 2021 3,060 3 View
Question to you and THEM, the New Journal, "Integrative Psychological and Behavioral Science" -- do you not know, and have you not seen, this done before? There appears to be a core problem for...
02 March 2021 3,024 2 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
Hello Everyone. Currently I am working to characterize macrophages in the myocardium after ischemia-reperfusion injury in rats. Due to the low total cell number isolated from rat hearts I can...
01 March 2021 3,867 3 View
We are preparing some experiments based on irradiating cells under different conditions in order to evaluate the effects in terms of DNA damage, genetic expression, etc. As our project is...
01 March 2021 3,355 3 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
Also when RHAMM binds hyaluronic acid, they get internalized, will RHAMM also be degraded? Or both CD44 and RHAMM will be transferred back to the cell membrane? Asking for breast cancer cell line...
01 March 2021 8,169 2 View
I'm a student and I have to produce a cell line with a knockin for the NRF2 gene with GFP. I have to put a promotor in front of the GFP because the gene will be too far away from the promotor of...
28 February 2021 7,127 2 View
I am aiming to determine the ADC values of a commercial fish feed, but I do not have a steam pelleter or extruder available to me. Ideally, the pellets could be coated with some inert marker....
28 February 2021 7,967 3 View
Im doing PBMC isolation -> CD14+ enrichment using magnetic beads -> stimulation setup. My negative control is just cells in cRPMI but they seem to get activated over and over again.
28 February 2021 7,883 3 View