The cells are flattened, adherent but debris is there so by the time they reach confluence, the debris is more.
How to recover them, dmem phenol red free plus insulin am putting.
Mycolplasma? But i need these cells badly and hw to check for mycoplasma
Hw will i recover the cells
Moreover they dont resemble in shape as mycoplasma,debris smallparticles not moving all over cells.
you can remove debris by different centrifugations. In my study, centrigation is done at 500 rpm 10' and there was no debris.
Ya i am doing same centrifuge same rpm and time it works but again the debris comes bk once theyreach confulency
Thanks shiv i will try to do that
In fact what if i can treat with antibiotic anti-mycotic fungizome in my m eida as recommended .5 % for 20x
Ok thankyou so much
I need these cells badly,i cant throw them,i used anti-mycotic yes,cell number was less but it cleared rest bit od debris,hopefully by pbs wash it will be clean.
I will have to work with mycoplasma protocol.let me observe cells.thanks
Say 1nm concentration?
10 November 2013 3,818 3 View
If you put IC50 of any cell line 15uM TAM in MCF-7 to create resistance, rather than going from the smallest concentration to the highest, is this a resistant cell line? In one month to three...
10 November 2013 5,058 1 View
What about p53 level in tam resistant cell lines with respect to parental mcf-7 cell line , is it the same or absent?
07 August 2013 4,444 0 View
Why is it difficult once the resistant cell line is made to revive the freezes? We can't just keep them running in culture, and if we change medium like from phenol red to phenol red free then to...
06 July 2013 474 11 View
How to reduce background in Western blot, per antibody for overnight at four degree or 1 hr at RT,then ,blocking 1 hr . Can I prolong blocking for 2 hrs,then wash with 1x pbst 5 mts each an dlast...
04 May 2013 2,003 9 View
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...
02 March 2021 9,945 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
Could you please recommend some good journal that accept very long revie papers (approximately 6000+ words) in neurosurgery, cancer biology ?
01 March 2021 8,087 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
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
Hi, I'm looking for data (mainly related to management: growth rate, canopy size, soil and climate preferences, etc.) about tropical trees used in tropical agroforestry. Have you ever heard about...
28 February 2021 7,356 8 View
Hi everyone, I am just wondering if we incubated 200 microliter of whole blood with 50 microliter of cancer cells(1bout 5000cells) do you think that cancer would survive for 48 hours?
23 February 2021 3,840 3 View
Hi Everyone, Has anyone here worked with MPC cell line? Any tips or tricks? I am just venturing into cell biology and any advice on this topic would be highly appreciated. Thank you so much. Niusha
22 February 2021 3,891 2 View
Hello dear scientists, Does the undifferentiated PC12 cell line in terms of chromosome characteristics, proliferation, and drug reactions have the characteristics of cancer cells? Where is it...
21 February 2021 8,945 3 View
I am using IZON qEV2 columns to isolate exosomes from 100 ml of cancer cell conditioned medium. in NTA analysis I usually see concentration of 2x10^9 particles/ml. But when I proceed with this...
20 February 2021 6,879 3 View