Ma'am you are an incredible proff how gifted u are in teaching so I wanted you more to upload on some videos.thank you ma'am I m really getting so many things from your teachings
Visit www.neelabakoretutorials.in for a well planned road map to help students score 360 marks in NEET Biology. Please share with those appearing for NEET.
Thank you so much ma'am.... students who can't afford for coachings can visit this .... I'll recommend about you whoever asks me how to understand biology concepts......i respect you and appreciate your efforts.. thank you Madam ❤️❤️
thnks.. i m getting a lot of help from it.. as my bio teacher got transferd to another school.. so i m using your videos to make my concepts.... thnks again :-)
@@udkmyname5251 proteins are different from dna as the dna goes through transcription and translation to produce protein. proteins are made of amino acids and dna is from nucleotides
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Southern blotting is named after British biologist Edwin Southern. So the the first letter of Southern blotting is capitalized....northern blotting and western blotting are not associated with names of any scientist but named so to keep similarity with 'Southern'.
Visit www.neelabakoretutorials.in for a well planned road map to help students score 360 marks in NEET Biology. Please share with those appearing for NEET.
prof. I would like to request you if you can upload some videos on how to read the phylogenetic tree and different types of selection in detail! I will appreciate it.
Maam I have a question how we decide which sequence should be der in a dna probe ??? Or if we take any random sequence how can v be sure that this random sequence is also present in our dna fragmets....
Visit www.neelabakoretutorials.in for a well planned road map to help students score 360 marks in NEET Biology. Please share with those appearing for NEET.
Hi mam.. I think u went wrong about this topic. Isoelectric focusing is used only in 2DGE but here we have only 1DGE process which is only based on electrophoretic mobility of nucleic acids which don't require pI .. as it has common surface negative charge.please go through it once again
Good evening ma'am. Your teaching is very excellent but I'm getting confused about sequential steps. Which step is first 2nd,3rd and so on especially in biotechnology. Please Clarify it madam.
When separating DNA fragments vertically on the basis of Density Centrifugation, are large DNA molecules stay up in the agarose gel or they are gonna come down as happens in heavy density..?
Mam...i have a question..from transfer assembly the Effinity of both gel and nitrocellulose is less the DNA but From nitrocellulose DNA was not moved and from gel DNA was moved why??
Visit www.neelabakoretutorials.in for a well planned road map to help students score 360 marks in NEET Biology. Please share with those appearing for NEET.
thanku so much mam my humble request for you to upload vedios about molecular markers particularly RFLP ,RAPD ... PLEASE MAM.. thanking you in anticipation
I m believe in self study and u help me a lot to gain a perfect knowledge
Ma'am you are an incredible proff how gifted u are in teaching so I wanted you more to upload on some videos.thank you ma'am I m really getting so many things from your teachings
The explanation is very simple manner, and I can easily caught the points. Thank you so much mam👍
Ma'am if we will have teacher like you in our schools we students will never miss any class and will love every subject ❤️
Visit www.neelabakoretutorials.in
for a well planned road map to help students score 360 marks in NEET Biology. Please share with those appearing for NEET.
Goddess Saraswati, as if descended on Earth!!
😊👍😌
really it is true bro/sis/trans
@@puneethnagaraj796 I'm glad, that u agreed with my notion, trans/sis/bro😊
Sorry sis i really disappointed seeing your replay
I shouldn't write that comment
@@puneethnagaraj796 🌝😌
This woman is so brilliant.. thank you ma'am
Tnak u mam.... Your teaching style really nice....... It helps me a lot
Thank you so much ma'am.... students who can't afford for coachings can visit this .... I'll recommend about you whoever asks me how to understand biology concepts......i respect you and appreciate your efforts.. thank you Madam ❤️❤️
Visit www.neelabakoretutorials.in
for a well planned road map to help students score 360 marks in NEET
thnks.. i m getting a lot of help from it.. as my bio teacher got transferd to another school.. so i m using your videos to make my concepts.... thnks again :-)
way of teaching is really awesome
Her approach is so captivating. She is a treasure.
Hi as far as I know, isoelectric focusing technique used for protein separation not for DNA
Ahmed Ali dts true
Well as far as I have understood proteins are segment of DNA and this method deals with the fragments of dna so it's proteins are basically 🧬 🙂
@@udkmyname5251 proteins are different from dna as the dna goes through transcription and translation to produce protein. proteins are made of amino acids and dna is from nucleotides
@@shreedhamji6554 true....yeah you're right
Ty for correcting 🥂
Hello guzs i am from food technology so can i right it same as she describe in examination?
Very good lectures madam
God bless you !
From srilanka 🇱🇰 🙏
Visit www.neelabakoretutorials.in
for a well planned road map to help students score 360 marks in NEET Biology. Please share with those appearing for NEET.
Theivame !! One like is not enough.👍
Southern blotting is named after British biologist Edwin Southern. So the the first letter of Southern blotting is capitalized....northern blotting and western blotting are not associated with names of any scientist but named so to keep similarity with 'Southern'.
Mam can you please add more video explanation for NET exam purpose because ur explanation is really easily understandable .
Thanku mam😊
you are incredible ma'am
ALLAH bless u .I always follow u ...now I'm lecturer botany
please do human health and disease
Thank you mam for spending hours in preparing this useful video
Maam aap itne easily samjhate ho😊
Ur examination is very nice & marvelous
Well understood mam.
Now clear 👍👍👍
Thank u soo much this helped me a lot in my exam hope I score well
Very nice and informative.
I love way you r teaching mam so accurate ....
your classes are really helpful
Thanku so much for the videos mam, but the ecology portion videos are not available on you tube plz upload videos of ecology also
ma'am you are teaching are so great
Asli teacher to ye hai 👌👌👌👌
Aaj kal koi kaam nahi mila to bas teacher ban jao
Bhale aata ho ya na ho
Paisa aana chaihiye 😠😠😠
thank you teacher...
Excellent teaching style. Thank you mam
Awsm nd thnku for dis tutorial 😊
please explain the interpretation of how to read results
Mam plz upload the blotting techniques
U make it all simple to understand thank-you mam
Thanks mem meri mem ne bhut difficult pdaya but Apne very easy Kiya
Mam u used term buffer here. which buffer we use here?
thank you mam...we got ideas very clearly
Thank you so much ma'am.. You are simply fabulous!!
Tq so much Mam ...we easily catch u r points..from bottom of my heart tq soooo much Mam..
very nice explanation of all the topics
What is eastern blotting?
Mam it's an excellent and wonderful class.Thankyou mam
Thank u soo much maam ....u r grrt ....love frm kashmir💚
Visit www.neelabakoretutorials.in
for a well planned road map to help students score 360 marks in NEET Biology. Please share with those appearing for NEET.
This video is very helpful for me... Thanks.....
Mam. Wat does ncert diagram 11.3 mean by digested and undigested dna?
Reealy informative..
mam please tells about agrobacterium tumefaciens genetic information and functions
prof. I would like to request you if you can upload some videos on how to read the phylogenetic tree and different types of selection in detail! I will appreciate it.
Maam I have a question how we decide which sequence should be der in a dna probe ??? Or if we take any random sequence how can v be sure that this random sequence is also present in our dna fragmets....
Ma'am I would like to bring to your notice that we do not dissolve agarose in distilled water instead we use TAE or TBE buffer.
.
What is buffer..
In my lab we always used distilled water to dissolve agarose. The buffer was only used in the electrophoresis.
@@MultiLeandrini S...right
Mam please give a chance to take screenshot..
Many students make notes from your videos
thanks madam for ur teaching
really nice.i naver give any coment any vedio i open my gmail and suscribe and like u know why . coz i understand all first time
thanku mam
mam can u plz explain bloting techniques.?.....plz mam...
Would be evn less if i thank u mam,seriously uve helped so much . Just cmplimented my self studies.still can juss thank .thnku so much
Dushyant Katara
what is a buffer?
Super awesome video. Many thanks! and one question: how do we know what DNA probe to put in?
Why we need to boil agarose? Rather than normal dissolving with buffer.
very useful video mam thank you so much😊
Aabha u look soo pretty💖💖
Mam plzz add a lecture on chromatography..it would be a great help.
AWESOME
.... FULLY HELPFUL.
THANK YOU
Please teach remaining lessons as much as possible 😍 😊 😋 😎 😊 mam please
thank you so much ma'am
Thank you so much mam this video is very useful.
Thank you mam ❤
Visit www.neelabakoretutorials.in
for a well planned road map to help students score 360 marks in NEET Biology. Please share with those appearing for NEET.
Hi mam.. I think u went wrong about this topic. Isoelectric focusing is used only in 2DGE but here we have only 1DGE process which is only based on electrophoretic mobility of nucleic acids which don't require pI .. as it has common surface negative charge.please go through it once again
yes exactly she need to correct it. IP does not imply for DNA molecule its for proteins
I would request you to read ncert pls
why DNA has different negative charge?
mam your study notes are not available on amazon as they are out of stock so mam can you please tell when would the notes be available again.
Buffer in transfer assembly is made of? How it goes up
Pls ans
How do you make probe for that DNA to which probe binds although u don't know the sequence !
Nice knowledge gained
I dont explain your importance but i told your talent somethin different.i am very very thankful
superb lec💖
Good evening ma'am. Your teaching is very excellent but I'm getting confused about sequential steps. Which step is first 2nd,3rd and so on especially in biotechnology. Please Clarify it madam.
which buffer is talked about here mam???
According to me two buffer were uesd....Tris borate EDTA and Tris acetate EDTA
Nice Explanation
Thank you madam 😇🙏🏻
your work is amazing and simplified.
When separating DNA fragments vertically on the basis of Density Centrifugation, are large DNA molecules stay up in the agarose gel or they are gonna come down as happens in heavy density..?
Thank you mam!!
Mam...i have a question..from transfer assembly the Effinity of both gel and nitrocellulose is less the DNA but From nitrocellulose DNA was not moved and from gel DNA was moved why??
So simply discussed, I am unable to say anything as I am already a bio teacher 🙏
Nice explaination
Mam u r like a god to me🙏🙏🙏🙏
Visit www.neelabakoretutorials.in
for a well planned road map to help students score 360 marks in NEET Biology. Please share with those appearing for NEET.
Mam can I ask a question that how is probe going to attach with DNA if DNA is double stranded???
it will not attach to dna instead it will go toward the dna and form hydrogen bond with it
due to which we can judge the sequence of other strand
Madam how can I get hard copy for Gel Electrophoresis Topic.
MAM what is flush ends,sticky& blunt ends can you give examples for these plz....MAM
Please make any other biotechnology lesson in mgkvp bsc 1st year syllabus
Ty neela maam.
excellent!
Woowww understood well
thanku so much mam
my humble request for you to upload vedios about molecular markers particularly RFLP ,RAPD ...
PLEASE MAM..
thanking you in anticipation
superb mam
thank you so much madam
I am new to this channel. Are these videos based on ncert reader, cbse board ?
what is buffer
Mam video 2 ,3 ,4 is not available
Can any one tell what is buffer about which maam is talking at 20:37
that can resist Ph change upon the addition of an acidic ao basic components
ma'am ur awsm
very explanation can share chromatography as well plzz