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?
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