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Dr. PREM-PRIMER Biotech Lectures
Индия
Добавлен 9 окт 2021
Since I am a researcher turned teacher, I use self-explanatory cartoons and animations to educate students about rDNA technology. I hope my presentations will serve you as a primer for your learning.
How many cells of the human body die per day
How many cells of the human body die per day
Просмотров: 34
Видео
Subtractive Hybridization
Просмотров 7021 день назад
Subtractive hybridization is a technique that removes the sequences of nucleic acid which are common in the two related samples, leaving behind the different sequences. This differentiates between the nucleic acid sequences (mRNA) expressed in two related samples in a specific a stage or condition. Subtractive hybridization mathematically subtracts the gene expression of treated tissue by using...
Compulsory Licensing, Bayer Vs Natco on Nexvar
Просмотров 45Месяц назад
Compulsory licensing is a legal mechanism that allows a third party to produce a patented product or process without the patent owner's consent. Normally the person or company applying for a Compulsory licensing has to have tried, within a reasonable period of time, to negotiate a voluntary licence with the patent holder on reasonable commercial terms In India, a compulsory license can be appli...
Normalized cDNA Library
Просмотров 763 месяца назад
cDNA Normalization: Methods to decrease the prevalence of highly abundant transcripts and equalize the transcripts concentration in cDNA library are called as cDNA Normalization Normalized cDNA library: Libraries in which disparity in the concentration of cDNAs molecules for various genes is smaller than initial disparity in concentration of cDNA or mRNA for those genes in the original sample
Features of Cloning and Expression Vectors
Просмотров 1856 месяцев назад
Features of Cloning and Expression Vectors
What is Biotechnology & Applications
Просмотров 928 месяцев назад
What is Biotechnology & Applications
Difference between Apoptosis and Necrosis Part-2
Просмотров 7011 месяцев назад
Difference between Apoptosis and Necrosis Part-2
Differences between Apoptosis and Necrosis part-1
Просмотров 10311 месяцев назад
Differences between Apoptosis and Necrosis part-1
Apoptosis: Defination, Morphological and biochemical features
Просмотров 19411 месяцев назад
Apoptosis: Defination, Morphological and biochemical features
Barren: Infertile, soil not good enough for plants to grow.
Просмотров 24Год назад
Barren: Infertile, soil not good enough for plants to grow.
cDNA Library: Constructions, Types and Vectors, Applications
Просмотров 367Год назад
cDNA Library: Constructions, Types and Vectors, Applications
Corollary: Natural Consequence of Something
Просмотров 15Год назад
Corollary: Natural Consequence of Something
Cantankerous: Bad tempered, always complaining
Просмотров 43Год назад
Cantankerous: Bad tempered, always complaining
What is Genomic Library: Definition and Construction
Просмотров 451Год назад
What is Genomic Library: Definition and Construction
Homopolymer tailing: DNA Joining Molecules
Просмотров 1,6 тыс.Год назад
Homopolymer tailing: DNA Joining Molecules
Linkers: Generation of Cohesive ends on DNA fragments
Просмотров 55Год назад
Linkers: Generation of Cohesive ends on DNA fragments
Differences Between Linkers and Adopters, Cloning of blunt End DNA fragments
Просмотров 90Год назад
Differences Between Linkers and Adopters, Cloning of blunt End DNA fragments
Adaptors: Joining Molecules, Blunt END DNA fragments cloning
Просмотров 258Год назад
Adaptors: Joining Molecules, Blunt END DNA fragments cloning
Linkers: Joining molecules, Cloning of Blunt DNA Fragments/ cDNA molecules
Просмотров 264Год назад
Linkers: Joining molecules, Cloning of Blunt DNA Fragments/ cDNA molecules
JAWAHARLAL NEHRU SCHOLARSHIPS FOR DOCTORAL STUDIES IN SOCIAL SCIENCE
Просмотров 57Год назад
JAWAHARLAL NEHRU SCHOLARSHIPS FOR DOCTORAL STUDIES IN SOCIAL SCIENCE
M13mp7 Cloning Vector: Symmetrical restriction sites
Просмотров 138Год назад
M13mp7 Cloning Vector: Symmetrical restriction sites
A
great video sir. thnakyou
Thank you, Happy learning
Such a good explanation
Thank you
Dr. Phem. How can i get intouch with you for consultation. Thank you
Hi there Thanks for your interest You can reach me via dnadeeds@gmail.com
It was really helpful to understand all principle. so nice explanation and easy to see the figures. Thank you very much. :)
Welcome & Thank you and try to subscribe to the channel for more updates.
Amazing,❤
Thank you
Hope you subscribed to the channel for more updates.
Yes I have
@@sujathaarun8376 thank you
Thank you for the well made lecture professor. I am also working as Asst. Professor Biotech,,,,thank you for excellent content...keep posting
Welcome sir, Wonderful to know that we belong to same community. I shall try to create content.
thank you very much keep going please
@@ElevaHer Welcome and happy learning
Cen 6 equal distribution
Why don't you talk in hindi?
@@Biology60___ hi, it won't be very effective in himdi
Well done, Sir! Thank you so much. This is really helpful.
Thank you & welcome. Try to subscribe to the channel for more updates
excellent class sir, thank you .
You are welcome, try to subscribe channel for more updates
Thank you for this video! Helped me a lot ! If I want to add a fusion protein so that I can increase the solubility of my protein, is the fusion protein inserted into the vector along with my gene? I got lost in the order of the plasmid construction steps..
Hi, Thanks for the nice comment You choose the Expression Vector with various tags (For example GST tag) to increase the solubility and stability of your protein. I suggest expression vector with GST tag may serve your purpose.
@@Dr.DNA-Primer thank you very much !
👍🏻
All the best
Can we use the baculovirus expression system to express the avian viral proteins?
Any gene can be expressed in baculovirus expression irrespective of the origin of gene. Try to subscribe channel to get regular updates.
Thank you sir
So nice of you
Very helpful 👍🏽
Thank you, don't miss updates of the channel try to subscribe. 😀
Thank you
Welcome🎉, do subscribe channel for updates
perfect
Thanks do subscribe for more updates
Thank you and do subscribe for more updates from channel
Great video
Thanks and try to subscribe for updates of channel
👍🏻👍🏻
🙏🙏🙏
Great explanation! Thank you.
Thank you & welcome
Good lecture. Also pl give a talk on engineered M13 phage for peptide synthesis
Thank you, soon I will give talk on that topic
thank you Dr.k for your great explanation
Welcome, try to consider my channel for subscription and will get you updates
👌 "promosm"
❤
Thank you sir 😊
Welcome
👍
🙏🙏🙏
Good presentation sir
Thank you 🙏 Sams Chemistry
It's an Amazing Explanation Sir, Thanks for the Video🙏🤝
Thank you and do subscribe for updates
@@Dr.DNA-PrimerSubscribed Sir, Thank you😇
All the best
Wow this video is very helpful sir... I hope you see my comment Your explanation is very good and crystal clear...your students are lucky to have you ❤
Thank you
Such as a wonderful explanation sir thank you ❤🎉😊
Welcome
Sir, what is single strain system in packaging of lambda cloning vector?
Mutation in Cos sites of Lamda DNA can not undergo replication but can synthesize all phage proteins. Such proteins are purified and mixed with recombinant lamda molecule and then phage particles are formed in vitro. Mutations in Cos sites lambda DNA phage strain is sufficient to pack the recombinant lamda DNA.
Tdt does not require template strand so it is called template independent polymerase ... sir does this involve in exonuclease activity
One of the variant of Mammalian TDT have 3'to 5' exonuclease activity
Thank you sir😊
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Sir I have seen your two videos on reverse transcriptase.. But I have a doubt reverse transcriptase enzyme need template OR not for synthesis of cDNA. If need template than which template
Hi, During the retroviral infection, by using Reverse transcriptase RNA is converted into double standard DNA and that is integrated into host genome. Eukaryotic mRNA will be used as template to synthesize cDNA by employing Reverse transcriptase.
@@Dr.DNA-Primersir reverse transcriptase requires a primer, which in the case of retroviruses, is a tRNA molecule bound at a specific site (the primer-binding site) close to the 5' terminus of the viral RNA
Yes
Good one..
Thank you
Sir I have a question, while making phagemid vector do we insert ss DNA fragment of M13 into the plasmid
No, double standard M13 fragment will be inserted. M13 genome converted into double standard that is called replicative form. Those replicative forms can be isolated.
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Thanks a lot sir 🙏 I was really confused about this
You are most welcome,
Sir, how primers are prepared chemically or using primase enzyme
Chemical Synthesis only
During in vivo replication primers are synthesized by primases only
For pcr and RT-Pcr chemically synthesized primers are used
@@Dr.DNA-Primer thank you sir
Did you subscribe me
18:43 sir u said that wrong nucleotide are added how they are corrected is their any proof reading activity
Generally Reverse transcriptase do not have 3' to 5' exonuclease activity (Proof reading activity) so no correction of wrong nucleotides added. Thanks
@@Dr.DNA-Primer thank you sir
Super sir
Thank you
Good explanation
Thank you
Thank you for explaining it so well.
Welcome and try to subscribe for updates
Nice presentation sir
Thank you
Liked and subscribed.too..it is very useful prem.
Thank you Sneha
Thank you so much sir for this lecture. ❣️
Welcome, Please share our videos with needy friends
Thank you Sir 😊
Most welcome
Sir i applied but i didn't get any email id
you did not get any mail from the Reliance foundation, wait few days or write to them
Can you please make a vedio of primer designing for PCR,RTPCR and sequencing. It will be helpful for many students
I will do certainly, I may take couple of weeks to do
The same fellowship is renewed after 6 month? becoz my father retire after three months then his income changed to less than 8 LPA.
Hello there, The applicant shall be the first year student of M.Sc/ Ph.D in lifesciences. After six months you may be in second year of M.Sc or Ph.D then you will not eligible. I am guessing for every one year there will be a notification from Bayer. Hope I answered to your question.
Sir i am very depressed i enroll phd in botany work on plant patho 1st year from pune university but i am in open category my father is teacher but my father dont me to do phd becouse as of now phd is expensive for them sir plz suggest me any other fellowship for open category.i need support if gov dont give me any fellowship may be i am give up next year.
Hi, please look for a part time teaching job and continue your Ph.D Programme. You can write the UGC-CSIR exam in the meantime. If you qualify for that and you will get fellowship for five years,