Very helpful. In college we use the play dough instead of cavity slide. I did this experiment 4 times and I couldn’t observe any motility. So my teacher couldn’t give me the mark. I think that’s because we fix the lens on 100x power , I will try again with 40x power. Thanx
I'm glad that this was helpful for you🙏🏼 Coming to your question... Yeah you can use Plasticine provided it should hold cavity slide and cover slip properly.
If you open the cover slip with sample of bacteria in air for a long time that u do now then bacteria could be change their character and started to reaction with environmental organisms...how can do u this process... sir??
Because bacterial sample we have taken on coverslip is now in inverted position against the cavity side.... when we we observe it under microscope ... Which results into drop hanging from coverslip
Heating the loop kills unwanted bacteria... So it becomes sterile (free from bacteria) and after cooling it...then it can be used to transfer bacteria of our choice....
No.. We have ro sterilize the loop.. We are doing many cultures and and we have to transfer many of the culture to cover slip.. So we have to sterilize it
This video is very helpful i will recommend it to my friends . The motility test was my weakness but not anymore.
I'm glad that this was helpful for you🙏🏼
Excellent explanation
Now my concept is clear and I can give viva without any fear
Thank you sir 😊
I'm glad that this was helpful for you🙏🏼
Best of luck for your Viva👍🏼
Very helpful. In college we use the play dough instead of cavity slide. I did this experiment 4 times and I couldn’t observe any motility. So my teacher couldn’t give me the mark. I think that’s because we fix the lens on 100x power , I will try again with 40x power. Thanx
I'm glad that this was helpful for you🙏🏼
Hi direct second year students
Very clear explanation sir. Thank you so much
I'm glad that this was helpful for you🙏🏼
Sir.. You have to off the bunsen burner flame
But sir why the video procedure are not displayed?
Sir , why we focuse the edge of the drop in this method ? 🤔🤔
There is higher probability of finding motile bacteria due to oxygen concentration at edge
@@the_bioway Thanks a lot sir 😊
“I like your video!”
Thanks
I have a doubt
When we have to observe slide under microscope .from
Which side we can observe
From cover slip or cover slip below the slide
You need to observe from the side where the cover slip is placed.
Wgat if there isnt any cavity , will we be able to observe bacteria mobility.
Thanks for this wonderful teaching
Glad it was helpful!
Superb sir
Wow ❤ Sir this was so interesting and helpful🎉thank you so much
Glad you liked it!
Sir is there any need of adding safranin in this procedure?
No. Not required
Sir you took another cover slip but didn't applied on slide na 😕
Awesome video sir
Plz tell the principle of hanging drop method.
Thank u Sir. Great explanation. One question, can plasticine be used in place of petroleum jelly?
I'm glad that this was helpful for you🙏🏼
Coming to your question... Yeah you can use Plasticine provided it should hold cavity slide and cover slip properly.
@@the_bioway Alright Sir, thanks😄
Hi malhari how are u
I love microbiology
If you open the cover slip with sample of bacteria in air for a long time that u do now then bacteria could be change their character and started to reaction with environmental organisms...how can do u this process... sir??
Sir Do we need to use the fresh broth for viewing motility assay ...or can we use the refrigerated broth also
Freshly prepared one.
But we are not dropping any thing than why its called as hanging drop method
Because bacterial sample we have taken on coverslip is now in inverted position against the cavity side.... when we we observe it under microscope ... Which results into drop hanging from coverslip
Excellent.. Thank you🙏💕
I'm glad that this was helpful for you🙏🏼
nice video sir, its really helpful
I’m glad that this was helpful for you 🙏🏼
Ham to fan ho gaye apke 🎉
I'm glad that this was helpful for you.🙏
Thank u so much sir the video was really helpful❤
I'm glad that this was helpful for you🙏🏼
Hlo is it possible to view the border in 40x too or in just 10x.. My teacher keeps asking for that in observation.. I'm not really able to get it.
At 40x or 10x you can see only the border but to see bacteria you need to go for higher magnification power
Thank you so much
I’m glad that this was helpful for you🙏🏼
Very informative video
I’m glad that this was helpful for you 🙏🏼
Thank you so much sir ❤️
I'm glad that this was helpful for you🙏🏼
excellent. thank you Sir.
I'm glad that this was helpful for you🙏🏼
Nice explanation...
I'm glad that this was helpful for you🙏🏼
Sir we can see any type of bacterial movement through this procedure?
Yes
Thanks
Sir please can Answer me the heating of loop donot kill bacteria ?
Heating the loop kills unwanted bacteria... So it becomes sterile (free from bacteria) and after cooling it...then it can be used to transfer bacteria of our choice....
Thank you sir god bless you
I'm glad that this was helpful for you🙏🏼
No.. We have ro sterilize the loop.. We are doing many cultures and and we have to transfer many of the culture to cover slip.. So we have to sterilize it
Heating of loop kya huta hai mam
I have a question
Why do bacteria move in edged
Bacteria move towards edge due to high oxygen concentration at edge
Tq so much for your certain help.
I'm glad that this was helpful for you🙏🏼
Why did u use petroleum jelly only to coverslip?
To make sure only corners of coverslip getting attached
Blie broth video link send Karo
How to do this experiment with solid media
You can refer following article for Motility Test using Semi-solid Media
microbeonline.com/tests-bacterial-motility-procedure-results/
@@the_bioway Tomorrow is our microbiology lab exam. But I'm still confused about making hanging drop from a solid media.
Hanging drop method doesn't use Solid Media.
God bless you💙
Incredible
Very nice 👌👌
I’m glad that this was helpful for you🙏🏼
Nice video
Thanks
I am worry for the subject from whom this sample is taken😩😩😩😭
Nice sir
I'm glad that this was helpful for you🙏🏼
Its helpful
I’m glad that this was helpful for you 🙏🏼
does this method need heat fixation?
No
Hiii
❤❤
Malhari how are u
💕💕💕
How to report?
Reporting is done as Motile, non-Motile and sluggishly Motile organisms
❤️
👍👍👍
Thanks
can I hear a cat in the background. I hope not.
Not at all... 😅
cats are great
ايزي😂😂😂😂😂😂😂😂😂😂😂😂😂😂😂😂
Thanks
Nice Sir
Nice video
I'm glad that this was helpful for you🙏🏼
❤