No video

Gene Cloning (LIVE DEMO)

  Рет қаралды 33,575

NEXT Bio

NEXT Bio

Күн бұрын

Пікірлер: 53
@TonyMontana-lm5gp
@TonyMontana-lm5gp Жыл бұрын
so my takeaway from this is ... Gene cloning involves the use of a cloning vector, such as pbr322, and the gene of interest. Both the vector and the gene are cut using restriction enzymes, such as EcoRI, leaving flanking ends for ligation. The ligation is performed in the presence of ligase at 16°C overnight. The host for the gene cloning is E. coli, specifically the DH5 alpha strain. On the first day, the host is revived and inoculated in Luria broth for overnight incubation at 37°C. The following day, competent cells are prepared and transformed using the recombinant DNA from the ligation. After transformation, the colonies are selected based on their fluorescence under UV light. Non-fluorescent colonies are recombinant, while glowing colonies are non-recombinant and have intact GFP genes. This is divided into three days: the first day for reviving the host and setting up the ligation, the second day for preparing competent cells and transformation, and the third day for colony selection. Bullet Points: - Gene cloning involves a cloning vector and a gene of interest - Both are cut using restriction enzymes and ligated in the presence of ligase - E. coli DH5 alpha is used as the host - The practical is divided into three days: host revival and ligation, competent cell preparation and transformation, and colony selection - Non-fluorescent colonies are recombinant, while glowing colonies are non-recombinant and have intact GFP genes. So far so good?
@myrkwood4741
@myrkwood4741 2 жыл бұрын
Always İndians! Its always İndians who helps us in any subject! Bless you!!! 🤗
@NirajSingh1979
@NirajSingh1979 2 жыл бұрын
Thank you..
@bailahie4235
@bailahie4235 2 жыл бұрын
Amazing that such a procedure that is a result of incredibly advanced scientific research by the scientific community, can just be carried out on a desk with a set of instruments that do not look too advanced at first glance... Thanks for showing !
@najibyahayasani1101
@najibyahayasani1101 2 жыл бұрын
Step by step explanation with ease. Thank You very much Sir.
@Zyy225
@Zyy225 2 жыл бұрын
Sir.. it's amazing to see a live demo of molecular cloning.. please make more videos on molecular cloning of proteins Sir🙏😊
@NirajSingh1979
@NirajSingh1979 2 жыл бұрын
Thank you
@BPUJAA
@BPUJAA 2 жыл бұрын
Thankyou for the detailed explanation.
@awnishkumar1294
@awnishkumar1294 2 жыл бұрын
Best video of cloning and transformation on KZbin
@TheLawsoniaLab
@TheLawsoniaLab Ай бұрын
Well explained! Thank you sir for this awesome video
@vivekmanyapu949
@vivekmanyapu949 2 жыл бұрын
So nicely elaborated and performed smoothly...🙏🏻🙏🏻
@sadafchaudhary6063
@sadafchaudhary6063 15 сағат бұрын
Thank you so much Sir...i am grateful for your help
@shobhasurbhaiyya3759
@shobhasurbhaiyya3759 2 жыл бұрын
Really very informative... Thank u sir... Great efforts
@ArtistRashmi11
@ArtistRashmi11 Жыл бұрын
It's a very amazing and informative video for an lab unexperienced students. Thanku for your efforts.
@AVmang
@AVmang 3 жыл бұрын
Nice effort.
@sangra2380
@sangra2380 Жыл бұрын
very help full video for my end sem practical thank you sir you r a "w person💪 "
@pranjalkumar5408
@pranjalkumar5408 2 жыл бұрын
We want more videos on Biotechnology sir ❤️
@NirajSingh1979
@NirajSingh1979 2 жыл бұрын
Sure... I will try to make more videos...
@karthigaarumugasamy8468
@karthigaarumugasamy8468 2 жыл бұрын
Well explained, thank you
@user-yh3rh5tj3c
@user-yh3rh5tj3c 6 ай бұрын
Great work Dr singh Lecture well understood
@pranjalkumar5408
@pranjalkumar5408 2 жыл бұрын
Awesome Explanation sir ❤️
@arindampaul3529
@arindampaul3529 Жыл бұрын
Excellent Sir, thank you for sharing this full procedure.
@NirajSingh1979
@NirajSingh1979 11 ай бұрын
Thank you
@JYOtiRaNJanMANgaRaj
@JYOtiRaNJanMANgaRaj 4 ай бұрын
THANK YOU SO MUCH 🙏🙏🙏🙏
@MIs-kj1px
@MIs-kj1px 2 жыл бұрын
thankyou sir for helping me with my final year project.
@navdeepkaur8721
@navdeepkaur8721 Жыл бұрын
Thankyou ...it takes a great effort to make a video. Keep up the good work. Understood really welll
@NirajSingh1979
@NirajSingh1979 11 ай бұрын
Thank you
@manithsiriwardana8724
@manithsiriwardana8724 Жыл бұрын
Thank you so much for making this video sir!
@dhrubasonowal5978
@dhrubasonowal5978 4 ай бұрын
sir it is really helpful..but want to ask you that the 4th step of the protocol which is incubate at 37C at 300 rpm had been missing in the video.... Please help me regarding this.
@padmajadeore3764
@padmajadeore3764 2 жыл бұрын
Thank you for the excellent experiment!
@sukomog6769
@sukomog6769 2 жыл бұрын
very detailed explanation.Thank you very much
@tusharkashyap1938
@tusharkashyap1938 6 ай бұрын
In P plate, you said that only the plasmid has been put for the cell to get transformed. Your plasmid had GFP as well as antiobiotic resistance gene, the how will you explain about those colonies in P plate which are not flourescent and yet resistant to the antibiotic? If they have antibiotic resistivity, the why they don't have the fluorescence?
@priyankapandya3839
@priyankapandya3839 2 жыл бұрын
Thank you sir..it was very informative
@SriranjiniAS
@SriranjiniAS Ай бұрын
If we have any personal queries or any sops we require. Can we ask your assistance?
@MICROTECT
@MICROTECT 7 ай бұрын
Hello sir. after ligation u incubate the reaction for 24 h but in our case we are using pcr clone jet kit and it's protocol suggest to incubate only 30 minutes
@asifiqbal1482
@asifiqbal1482 6 ай бұрын
Sir make practical video on Elisa
@prernasingh8133
@prernasingh8133 2 жыл бұрын
Sir, I Truly admire your explanation and it was so clear. But, I could not resist commenting the fact that the personnel protection was completely off here. As a teacher, you must encourage wearing gloves while handling microorganisms. This experiment could have gone wrong in so many ways for instance, you were opening vials using the hand which the pipette due to which your tip was swinging in air and touching the surface thus bringing in contamination of nucleases. Also, its a fire hazard to use a burner inside a laminar hood/biological safety cabinet. Please don't take this wrong, I just mentioned all this because young students curiously watch such videos and end up getting the wrong idea about personal protection while working in the lab. It's a request that you kindly use proper gloves and try opening vials with your left hand as you hold the pipette in right. Thanks! Great explanation :)
@NirajSingh1979
@NirajSingh1979 2 жыл бұрын
Yeah you are true... Actually this video was made during COVID period for students and that time there was huge scarcity of personal protective equipments!!!!! Anyway thanks for your comments...
@prernasingh8133
@prernasingh8133 2 жыл бұрын
@@NirajSingh1979 thank you for the response. Yes, covid situation explains a lot. I hope to see more videos from you 😊have a nice day!
@ammarahchaudhary2820
@ammarahchaudhary2820 Жыл бұрын
Sir ARMS pcr aur nested pcr ka bhi video bana dy.
@plaharika525
@plaharika525 2 жыл бұрын
Thank you sir 🙏
@Farhab
@Farhab 11 ай бұрын
Awesome
@komalsonawane1995
@komalsonawane1995 Жыл бұрын
Hello sir....I want to know if all the procedures need to be done in sterile condition after the 3 steps you mentioned for viable cells..? how to maintain that condition? Or not needed?
@komalsonawane1995
@komalsonawane1995 Жыл бұрын
You have not taken od before the centrifugation step...
@cutychandanacastle19
@cutychandanacastle19 Жыл бұрын
Very nice video. Thank you. Please use gloves. For safety.
@NirajSingh1979
@NirajSingh1979 Жыл бұрын
Thanks for your suggestions. These videos are made during Covid crisis when gloves were not available in the market
@vandanagautam9998
@vandanagautam9998 Жыл бұрын
sir.. can we use colony pcr to check transformed bacterias?
@NirajSingh1979
@NirajSingh1979 11 ай бұрын
Yes, ofcourse we can...
@sadaftagar220
@sadaftagar220 Жыл бұрын
sir can we this plasmid dna as an standard in real time pcr?
@NirajSingh1979
@NirajSingh1979 11 ай бұрын
Yes
@narmeenmaqsoodtr8883
@narmeenmaqsoodtr8883 2 жыл бұрын
Sir is it non kit method of cloning?
@NirajSingh1979
@NirajSingh1979 2 жыл бұрын
Yeah, in some portions kit materials has been used..... It is combination of kit and non kit...
@arohishermale515
@arohishermale515 2 жыл бұрын
Thank you sir
Extracting Plasmid DNA: How To Do a Miniprep
15:33
LabXchange
Рет қаралды 57 М.
Gene Cloning with the School of Molecular Bioscience
22:23
The University of Sydney
Рет қаралды 160 М.
Magic trick 🪄😁
00:13
Andrey Grechka
Рет қаралды 67 МЛН
Now it’s my turn ! 😂🥹 @danilisboom  #tiktok #elsarca
00:20
Elsa Arca
Рет қаралды 11 МЛН
managed to catch #tiktok
00:16
Анастасия Тарасова
Рет қаралды 54 МЛН
Immunology in the skin
7:30
nature video
Рет қаралды 2,9 МЛН
Key Steps of Molecular Cloning
7:20
Andriy Nemirov
Рет қаралды 375 М.
How to Make Chemically Competent E. coli
15:21
Synthetic Biology One
Рет қаралды 50 М.
How CRISPR lets us edit our DNA | Jennifer Doudna
15:54
TED
Рет қаралды 1,8 МЛН
Molecular cloning overview - techniques & workflow
35:51
the bumbling biochemist
Рет қаралды 40 М.
Mammalian cell culture
23:37
Neil Cross
Рет қаралды 100 М.
Steps in Gene Cloning || A Complete Comprehensive Concept Video
16:54
Restriction Cloning
23:40
Katharine Hubbard
Рет қаралды 17 М.