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Questions related from Govardhan Bale
i did whole exmoe sequencing using (NGS) ion Proton system .. i have the patients and control data... need suggestion and the pipelines filters for data analysis how to avoid and know the false...
08 August 2017 5,381 1 View
I usually use distilled water for primer dilution, i never got problem but one of GC rich (63%) primer getting degraded often. which one can be better for GC rich primer dilution TE or water if TE...
07 July 2017 2,990 26 View
hi i found a change in the morphology of min6 cells while doing GSIR. some cells even got lifted from the plate. is this common while performing the GSIR using Min6 cells?
09 September 2015 2,758 0 View
Hi I generally do GSIR by static method. Recently i found Perifusion method to study insulin release. So what is the difference between these two methods and which is more reliable? Thanks
07 July 2015 3,430 0 View
I have some frozen RNA samples in -80 and I want to do cDNA synthesis fallows qRT-PCR. I am using DNase I from genei i want use EDTA for deactivation of Dnase I after treatment with RNA thank you..
02 February 2015 9,868 4 View
When i check RNA purity the peak height at 260 or 280nm is less than the peak height at 230nm or other nm.
12 December 2012 1,912 10 View
Can anyone recommend a protocol for quantitative estimation of bile salts in bile sample?
03 March 2012 7,708 2 View
if i will run the gel of that PCR product did i will get any band ?
01 January 2012 9,175 15 View
The problem is biological sample having bile pigments, it interfering while estimating the cholesterol..
01 January 2012 8,065 16 View
Based on colorimetric method or any other method
01 January 2012 5,777 0 View
ELISA reader at particular nm length absorbs only one color or more ?? EX : at 505 nm length it absorbs pink if i will put yellow color reaction sample its giving high value than pink color. why...
12 December 2011 7,709 2 View
If i will use calorimetric/sepc method bile pigments also give some color to reaction
10 October 2011 6,942 0 View