for the solid sample, if I pour sterile liquid into the stomacher bag and stomach with the solid food, does that means after stomacher, the liquid itself is already 10^-1 ?
In 7:06 when last 4 dilutions were transfered to petri plates, how much quantity of dilutions was used to transfer n why only last four dilutions were transfered, not all?? Kindly answer
That petri dish looks like a galaxy of different milky ways... Can you make a video on how to isolate multiple bacteria in one petri dish from a sample that contains multiple bacteria?
look for morphology ,color of the colonies in same petriplates.Mark it.Prepare nutriet agar and pour to petridish. Pick the colony and do quadrant straking .If not make slants in test tube.
basically she is doing the exiperiment outside of the laminar airflow. then how would they say that do aseptic techniques automatically that will be got contamination. thank you. But thanks for the lecture its more informative.
Will you please reply for this doubt that I'm having... Why we always take the reciprocal of the dilution factor (eg:- 10^6 instead of 10^-6 )while multiplying it with no. of colonies for getting CFU count ?
Thank you so much for putting together this tutorial. It’s very helpful for my online Microbiology class 👏
Been looking for a video that talked about a solid sample. Thanks.
Excellent method for juniors please carry on the world need u thanks for all
Thank you so much this tutorial really help me alot as am using this method to isolate bacteria for my undergraduate project
It was very clearly explained. Thank you for giving knowledge for us🙏.
This was so detailed ,thank you so much ,keep up the good work 👏
Thanks for the teaching I appreciate it's so explanatory and clear
thankyou so much for simplifying this aspect, it was hectic for me..
This would definitely help in my project work, I’m working on Fungi isolates
Thanks for providing such a well explained video
Very well explained each aspect in the video. Thank you.
Thank you so much for excellent explanation
for the solid sample, if I pour sterile liquid into the stomacher bag and stomach with the solid food, does that means after stomacher, the liquid itself is already 10^-1 ?
In 7:06 when last 4 dilutions were transfered to petri plates, how much quantity of dilutions was used to transfer n why only last four dilutions were transfered, not all?? Kindly answer
1 ml of sample.
Very illustrative
Thanks very well explained .a lay man can also understand this
That petri dish looks like a galaxy of different milky ways... Can you make a video on how to isolate multiple bacteria in one petri dish from a sample that contains multiple bacteria?
look for morphology ,color of the colonies in same petriplates.Mark it.Prepare nutriet agar and pour to petridish. Pick the colony and do quadrant straking .If not make slants in test tube.
@@inactive392 That seems like a valid idea, thanks.
Thanks for very will explain.
we understand easily.
excellent explanation, thank you lecturer
Glass rod spreading plate technique and pour plate technique 👉 can get same result?
Thanks for a good explanation.
Thank you very much
GREAT VIDEO!!
Thankyou fr this video.
How much inoculum to use to pour on the Petri dish
0.1 preferably
useful video,thanks
Great comment Furkan Purplerose ! Good luck.
@@DenizY18 thanks to our teacher for these opportunities
Please suggest me which media is suitable for fecal coliform test by pour plate method and how we can prepare this media?
Thank you find this vedeo very helpful to me 🙏👍💗💗
Very helpful
So helpful thank you ❤
thank u very mach guys
by such far distance from flame my samples got contaminated if i close pippete near flame while making dilution pipette burns what to do😣
Minimize the time that the petri dish lid is off.
I love this
best explanation
Thank you
Thank you!
Thanks
Very clear
Good video
Thank you somuch...its quite understood.
Thank you 👍👍❤
how many colonies are there in each petri dish?
How to convert cfu/g to cfu/ml
Hi Microbial zoo.......how much amount of diluted sample is mixed with melted agar medium...??
Thank you for the nice video...🙌🏼
Great
basically she is doing the exiperiment outside of the laminar airflow. then how would they say that do aseptic techniques automatically that will be got contamination. thank you. But thanks for the lecture its more informative.
aseptic technique requirements are met by manipulating samples near the Bunsen burner
ga bisa basa enggres, tugasnya kek gini, gils semangat kawan ngabrio kuu
untung tadi gaada absen gan, rodok ndredeg yo lur
Will you please reply for this doubt that I'm having...
Why we always take the reciprocal of the dilution factor (eg:- 10^6 instead of 10^-6 )while multiplying it with no. of colonies for getting CFU count ?
in this vedio bacteria has not been inoculated
Very gd
Tolong terjemahan ke bahasa indonesia!!
Ni mulele oglo