Dr. PREM-PRIMER Biotech Lectures
Dr. PREM-PRIMER Biotech Lectures
  • Видео 113
  • Просмотров 71 723
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...
Patent obtaining procedure in India
Просмотров 62Месяц назад
Patent obtaining procedure in India
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
What is rDNA Technology
Просмотров 1218 месяцев назад
What is rDNA Technology
Bcl2 and Caspases: Apoptosis
Просмотров 9811 месяцев назад
Bcl2 and Caspases: Apoptosis
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
Mitosis:
Просмотров 110Год назад
Mitosis:
Trailblazer:
Просмотров 48Год назад
Video from dnadeeds
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
cDNA Synthesis from RNA
Просмотров 3,6 тыс.Год назад
cDNA Synthesis from RNA
What is Genomic Library: Definition and Construction
Просмотров 451Год назад
What is Genomic Library: Definition and Construction
What is Genome
Просмотров 70Год назад
What is Genome
what is DNA Cloning I: Summary
Просмотров 69Год назад
what is DNA Cloning I: Summary
DNA CLONING II: Methods and Strategies
Просмотров 99Год назад
DNA CLONING II: Methods and Strategies
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

Комментарии

  • @thallapellisravan8465
    @thallapellisravan8465 13 дней назад

    A

  • @Crackitwinit
    @Crackitwinit Месяц назад

    great video sir. thnakyou

  • @anjalisingh-tt9cm
    @anjalisingh-tt9cm 2 месяца назад

    Such a good explanation

  • @teklasmom4156
    @teklasmom4156 2 месяца назад

    Dr. Phem. How can i get intouch with you for consultation. Thank you

    • @Dr.DNA-Primer
      @Dr.DNA-Primer 2 месяца назад

      Hi there Thanks for your interest You can reach me via dnadeeds@gmail.com

  • @Dan-qn7lf
    @Dan-qn7lf 3 месяца назад

    It was really helpful to understand all principle. so nice explanation and easy to see the figures. Thank you very much. :)

    • @Dr.DNA-Primer
      @Dr.DNA-Primer 3 месяца назад

      Welcome & Thank you and try to subscribe to the channel for more updates.

  • @sujathaarun8376
    @sujathaarun8376 3 месяца назад

    Amazing,❤

  • @huga1991
    @huga1991 3 месяца назад

    Thank you for the well made lecture professor. I am also working as Asst. Professor Biotech,,,,thank you for excellent content...keep posting

    • @Dr.DNA-Primer
      @Dr.DNA-Primer 3 месяца назад

      Welcome sir, Wonderful to know that we belong to same community. I shall try to create content.

  • @ElevaHer
    @ElevaHer 4 месяца назад

    thank you very much keep going please

    • @Dr.DNA-Primer
      @Dr.DNA-Primer 4 месяца назад

      @@ElevaHer Welcome and happy learning

  • @Exploria7
    @Exploria7 5 месяцев назад

    Cen 6 equal distribution

  • @Biology60___
    @Biology60___ 5 месяцев назад

    Why don't you talk in hindi?

    • @Dr.DNA-Primer
      @Dr.DNA-Primer 5 месяцев назад

      @@Biology60___ hi, it won't be very effective in himdi

  • @utibeimaevans629
    @utibeimaevans629 6 месяцев назад

    Well done, Sir! Thank you so much. This is really helpful.

    • @Dr.DNA-Primer
      @Dr.DNA-Primer 6 месяцев назад

      Thank you & welcome. Try to subscribe to the channel for more updates

  • @cheshtasharma424
    @cheshtasharma424 7 месяцев назад

    excellent class sir, thank you .

    • @Dr.DNA-Primer
      @Dr.DNA-Primer 7 месяцев назад

      You are welcome, try to subscribe channel for more updates

  • @vtrindade
    @vtrindade 7 месяцев назад

    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..

    • @Dr.DNA-Primer
      @Dr.DNA-Primer 7 месяцев назад

      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.

    • @vtrindade
      @vtrindade 7 месяцев назад

      @@Dr.DNA-Primer thank you very much !

  • @beepanginavadeep2081
    @beepanginavadeep2081 9 месяцев назад

    👍🏻

  • @noreenbashir3936
    @noreenbashir3936 10 месяцев назад

    Can we use the baculovirus expression system to express the avian viral proteins?

    • @Dr.DNA-Primer
      @Dr.DNA-Primer 10 месяцев назад

      Any gene can be expressed in baculovirus expression irrespective of the origin of gene. Try to subscribe channel to get regular updates.

  • @Singapangapavanteja
    @Singapangapavanteja 11 месяцев назад

    Thank you sir

  • @smrithiragothaman1695
    @smrithiragothaman1695 11 месяцев назад

    Very helpful 👍🏽

    • @Dr.DNA-Primer
      @Dr.DNA-Primer 11 месяцев назад

      Thank you, don't miss updates of the channel try to subscribe. 😀

  • @chupperschomps
    @chupperschomps Год назад

    Thank you

    • @Dr.DNA-Primer
      @Dr.DNA-Primer Год назад

      Welcome🎉, do subscribe channel for updates

  • @anahitaaghazadeh
    @anahitaaghazadeh Год назад

    perfect

    • @Dr.DNA-Primer
      @Dr.DNA-Primer Год назад

      Thanks do subscribe for more updates

    • @Dr.DNA-Primer
      @Dr.DNA-Primer Год назад

      Thank you and do subscribe for more updates from channel

  • @kofipapa2886
    @kofipapa2886 Год назад

    Great video

    • @Dr.DNA-Primer
      @Dr.DNA-Primer Год назад

      Thanks and try to subscribe for updates of channel

  • @drswethav
    @drswethav Год назад

    👍🏻👍🏻

  • @shamssaad9583
    @shamssaad9583 Год назад

    Great explanation! Thank you.

  • @krupanidhi912
    @krupanidhi912 Год назад

    Good lecture. Also pl give a talk on engineered M13 phage for peptide synthesis

    • @Dr.DNA-Primer
      @Dr.DNA-Primer Год назад

      Thank you, soon I will give talk on that topic

  • @ccs44
    @ccs44 Год назад

    thank you Dr.k for your great explanation

    • @Dr.DNA-Primer
      @Dr.DNA-Primer Год назад

      Welcome, try to consider my channel for subscription and will get you updates

  • @remy9548
    @remy9548 Год назад

    👌 "promosm"

  • @Jampularamesh
    @Jampularamesh Год назад

  • @VijjuMahankali
    @VijjuMahankali Год назад

    Thank you sir 😊

  • @sams_chemistry
    @sams_chemistry Год назад

    👍

  • @sams_chemistry
    @sams_chemistry Год назад

    Good presentation sir

  • @gayathriswedhika2442
    @gayathriswedhika2442 Год назад

    It's an Amazing Explanation Sir, Thanks for the Video🙏🤝

  • @Biotechie_Concepts
    @Biotechie_Concepts Год назад

    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 ❤

  • @vijjumahankali4297
    @vijjumahankali4297 Год назад

    Such as a wonderful explanation sir thank you ❤🎉😊

  • @shalink.sharma2190
    @shalink.sharma2190 Год назад

    Sir, what is single strain system in packaging of lambda cloning vector?

    • @Dr.DNA-Primer
      @Dr.DNA-Primer Год назад

      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.

  • @vijjumahankali4297
    @vijjumahankali4297 Год назад

    Tdt does not require template strand so it is called template independent polymerase ... sir does this involve in exonuclease activity

    • @Dr.DNA-Primer
      @Dr.DNA-Primer Год назад

      One of the variant of Mammalian TDT have 3'to 5' exonuclease activity

  • @vijjumahankali4297
    @vijjumahankali4297 Год назад

    Thank you sir😊

    • @Dr.DNA-Primer
      @Dr.DNA-Primer Год назад

      Try to subscribe for more updates from channel

  • @KrishnaKrish-m8s
    @KrishnaKrish-m8s Год назад

    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

    • @Dr.DNA-Primer
      @Dr.DNA-Primer Год назад

      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.

    • @KrishnaKrish-m8s
      @KrishnaKrish-m8s Год назад

      @@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

    • @Dr.DNA-Primer
      @Dr.DNA-Primer Год назад

      Yes

  • @dr.someswarr.sagurthi6993
    @dr.someswarr.sagurthi6993 Год назад

    Good one..

  • @rashmipandey7425
    @rashmipandey7425 Год назад

    Sir I have a question, while making phagemid vector do we insert ss DNA fragment of M13 into the plasmid

    • @Dr.DNA-Primer
      @Dr.DNA-Primer Год назад

      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.

    • @Dr.DNA-Primer
      @Dr.DNA-Primer Год назад

      Do subscribe for more updates

    • @rashmipandey7425
      @rashmipandey7425 Год назад

      Thanks a lot sir 🙏 I was really confused about this

    • @Dr.DNA-Primer
      @Dr.DNA-Primer Год назад

      You are most welcome,

  • @KrishnaKrish-m8s
    @KrishnaKrish-m8s Год назад

    Sir, how primers are prepared chemically or using primase enzyme

    • @Dr.DNA-Primer
      @Dr.DNA-Primer Год назад

      Chemical Synthesis only

    • @Dr.DNA-Primer
      @Dr.DNA-Primer Год назад

      During in vivo replication primers are synthesized by primases only

    • @Dr.DNA-Primer
      @Dr.DNA-Primer Год назад

      For pcr and RT-Pcr chemically synthesized primers are used

    • @KrishnaKrish-m8s
      @KrishnaKrish-m8s Год назад

      @@Dr.DNA-Primer thank you sir

    • @Dr.DNA-Primer
      @Dr.DNA-Primer Год назад

      Did you subscribe me

  • @KrishnaKrish-m8s
    @KrishnaKrish-m8s Год назад

    18:43 sir u said that wrong nucleotide are added how they are corrected is their any proof reading activity

    • @Dr.DNA-Primer
      @Dr.DNA-Primer Год назад

      Generally Reverse transcriptase do not have 3' to 5' exonuclease activity (Proof reading activity) so no correction of wrong nucleotides added. Thanks

    • @KrishnaKrish-m8s
      @KrishnaKrish-m8s Год назад

      @@Dr.DNA-Primer thank you sir

  • @dsanthosh1450
    @dsanthosh1450 Год назад

    Super sir

  • @dr.someswarr.sagurthi6993
    @dr.someswarr.sagurthi6993 Год назад

    Good explanation

  • @ankitamalakar8993
    @ankitamalakar8993 Год назад

    Thank you for explaining it so well.

    • @Dr.DNA-Primer
      @Dr.DNA-Primer Год назад

      Welcome and try to subscribe for updates

  • @sams_chemistry
    @sams_chemistry Год назад

    Nice presentation sir

  • @snehaselections3811
    @snehaselections3811 Год назад

    Liked and subscribed.too..it is very useful prem.

  • @rincyaugustine3354
    @rincyaugustine3354 Год назад

    Thank you so much sir for this lecture. ❣️

    • @Dr.DNA-Primer
      @Dr.DNA-Primer Год назад

      Welcome, Please share our videos with needy friends

  • @johnfanai2038
    @johnfanai2038 Год назад

    Thank you Sir 😊

  • @pallavipinku3195
    @pallavipinku3195 Год назад

    Sir i applied but i didn't get any email id

    • @Dr.DNA-Primer
      @Dr.DNA-Primer Год назад

      you did not get any mail from the Reliance foundation, wait few days or write to them

  • @vanitha294
    @vanitha294 2 года назад

    Can you please make a vedio of primer designing for PCR,RTPCR and sequencing. It will be helpful for many students

    • @Dr.DNA-Primer
      @Dr.DNA-Primer 2 года назад

      I will do certainly, I may take couple of weeks to do

  • @karinanamorefacemarathonfr503
    @karinanamorefacemarathonfr503 2 года назад

    The same fellowship is renewed after 6 month? becoz my father retire after three months then his income changed to less than 8 LPA.

    • @Dr.DNA-Primer
      @Dr.DNA-Primer 2 года назад

      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.

    • @karinanamorefacemarathonfr503
      @karinanamorefacemarathonfr503 2 года назад

      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.

    • @Dr.DNA-Primer
      @Dr.DNA-Primer 2 года назад

      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,