Thanks a lot David. I am planning to do this experiment in our lab for the first time. Your demonstration made me feel confident. Cheers
@zarinhaidernodi9622 Жыл бұрын
It was e.coli????
@Mayanfull4 жыл бұрын
Thanks!! I needed a reminder and this was very useful!
@MahdiHemmati-gi9rw4 ай бұрын
Can I autoclave it before use to skip the ethanol part?
@alisaleh19872 жыл бұрын
thank you s🇮🇶Thank you, sir. I am from Iraq, and this lesson we have is in biology Thank you very much
@arunkalaivanan80752 жыл бұрын
sir, i have doubt, about why there is moisture alone with the bacterial colony in the end pic?
@farahali4633 жыл бұрын
u r so good, thank u bc of u I'll take a very good score in the exam
@MrWhangdoodles7 ай бұрын
Excellent video.
@Mahdi-xk7ib2 ай бұрын
It is very helpful ❤
@vetberrypk3 жыл бұрын
What should be the temperature inside incubator ?
@josephgaleno50983 жыл бұрын
Little late but typically E.coli on petridish can grow at 35c. At this temperature, you should be able to see growth within 24 hours.
@davecummings63282 жыл бұрын
usually 37C, but that depends on the species of bacteria.
@sushamapawar58422 жыл бұрын
I also watch your vidios pleas give a way after dmlt diploma in medical lab tech. Need your guidance sir
@sushamapawar58422 жыл бұрын
I also watch your vidios pleas give a way after dmlt diploma in medical lab tech. Need your guidance sir
@sawairagul2514 жыл бұрын
Well explained 👌🏼
@lauryngrcic62372 жыл бұрын
What about the very small amount of inoculum that is inevitably left on the spreader tool? Doesn't that loss of volume affect your CFU calculation if the true volume isn't delivered to the plate? Why doesn't the loss of volume matter?
@davecummings63282 жыл бұрын
Hi Lauryn. You could try to calculate how much is lost based on surface area of the spreader and surface tension of the broth. But my guess is that it's a few uL and the change in colony count is probably well within the error of the technique anyway. All that is to say that I don't think it would impact your results significantly.
@user-wk2gp3tu8h3 жыл бұрын
Thank you 💯💯
@byronmunashe38272 жыл бұрын
Well explain.👍👍👍👍👍
@sarekaya48152 жыл бұрын
I tried this method, but the bacteria did not grow as colonies, they grew in the whole plate and I could not count the colonies. What is the reason? thanks
@fukyoutubestupidfuckinghandles2 жыл бұрын
This method covered the whole plate so that's how it grew. This method isn't for counting colonies.
@fukyoutubestupidfuckinghandles2 жыл бұрын
streak plate method might be better but ive just started so there's probably a better method i dont know
@ashlykraphy99332 жыл бұрын
Sare kaya, You probably need to dilute the sample more so that you get it in countable range which is 20-200 for spread plating technique.