Thank you for your video! Not many TH-camr posted these kind of information, which may be understood as people were not interested in "heavy" academical videos. But, lately, because I really need information about Direct Plating and its feature, your video just showed up and helped me --insyaAllah. Thank you!
This video deserves at least a million views!
Nicely explained... Thank you sooo much
Thank you so much this video was the best one i have seen so far!!!
Thank you so much. This helped me a lot!
Thank you
If i use the top agar method, will i get satellite colonies? do i count them? or i only count the big colonies
This is an amazingly clear video to understand the spreading and streaking techniques completely. Thank you a lot, it was really helpful
Can I apply same method on fungi?.
especially Metarhizium on spread plate method?
So for all the dilutions the original inoculum would be same?...
Thank you for your video! Not many TH-camr posted these kind of information, which may be understood as people were not interested in "heavy" academical videos.
But, lately, because I really need information about Direct Plating and its feature, your video just showed up and helped me --insyaAllah. Thank you!
If we take 0,1 mL of the 4th tube to the plate, what will CFU/ml be?
I wished you could be my lecturer in the first place!
Well explained 👌🏼
Thanks i did not found the link??
Explained so well! So helpful, thankyou!
Thank you very much !
excellent explanation
very helpful!! Thnk u :D
is this applicable for fungi also?
To the yeast. if they form hyphae they might spread and you will not be able to isolate single colonies.
I want to thank you.
And I think that there are some "hm 'kays" to much..
Couldn't find a way to put that more humanly..
No problem! I do know I do that, just a weird habit.
This was incredibly helpful! Thank you.
Real helpful.thank you!