15 Questions 21 Answers 0 Followers
Questions related from Milad Esmaeilbeigi
for example in gill tissue, considering number of lamella(each treatment 500 lamella).
05 May 2015 4,547 4 View
i mean are chemical compounds of lysis buffer able to damage, probably. lysis solution include: (2.5 M NaCl, 0.1 M EDTA, 10 mM Tris, 1% Triton X-100, 9% DMSO, pH 10)
05 May 2015 5,451 7 View
i.e. Instead of using the big and mature fish, small and immature fish such as juvenile and fingerling used
02 February 2015 1,576 11 View
Recently I have captured new images with fluorescent microscope. I attached several images, can you comment on these?
01 January 2015 1,905 11 View
in fact I want using gill and liver cells.
01 January 2015 2,326 2 View
these fish are not mature and me want to separation it for propagation
01 January 2015 8,565 3 View
if possible, attaching a file for this method please.
01 January 2015 1,863 3 View
i used 10 microliter ethidium bromide for each loaded samples(two) on slide(i.e 20 microliter for each slide) but under the fleurosent microscope, can hardly see the halo DNA or comet. One of the...
01 January 2015 5,227 3 View
i want cutting the gill and liver tissue of fish
01 January 2015 5,714 13 View
Micronucleus assay to be carried out on fish. I am attaching several images, Please tell us your opinion.
01 January 2015 5,471 5 View
i mean: Destruction slides by light decomposition
12 December 2014 6,508 4 View
i want expose toxicant substances on fish red blood cells.
12 December 2014 3,292 2 View
I would like to know exactly what happens in the cell cycle?
12 December 2014 6,760 16 View
as regards that etidum bromide stain is very sensitive to light
12 December 2014 2,945 4 View
in slides under microscope, only parts of the tissue or other things are found and the comet tail is not found.
12 December 2014 4,185 3 View