i want to treat the bacteria with drugs and then check the viability of the cells
PubMed: https://www.ncbi.nlm.nih.gov/pubmed
Query: "MTT assay"[title/abstract] and "bacteria"[title/abstract]
Article A colorimetric assay for quantitating bovine neutrophil bact...
If you're using a kit for that, then you can just follow the supplied protocol.
since i am gonna give two diferent drug treatments in a single assay, there is a wash step required in between. moreover, my cells are in suspension rather than adherent. this puzzles me how can i wash the cells in a 96 well-plate.
I need a hypothetical example as an answer for my question for a better understanding. After getting the absorbance values of the protein samples by DNPH method, how can i express my results in...
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i am treating cells with different concentrations of drug. now that i want to use the drug as a control in MTT assay, what concentration of drug should i keep as a control? plz suggest
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i am working on bacterium, Deinococcus radiodurans
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Western blot, serum sample
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I added loading buffer of 2ul with DTT, and Bromophenol blue with 10ul of serum, but serum solidified after 5 minutes at 95C heating.
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I have to proceed for digestion where the plasmid yield is not sufficient.
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Hi all, I am validating a polyclonal antibody raised against human ANT4, through WB and ICC. In most of my controls, the antibody shows very little off-target binding, but when I pre-incubate the...
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I need to prepare a solution of Napabucasin (inhibitor of cancer cell stemness) in dichloromethane. The drug is expensive, so maybe somebody already tried to do it. If it is soluble, what is the...
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im working now on TPV solar cells and metamaterials and i realy need our help in CST microwave i have a tpv cell simulation and i want to extract particullarly the absorbtion of only the active...
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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...
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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...
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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...
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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.
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