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How to Design Primers for PCR 

Addgene
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Are you looking to design a primer for your PCR? Jennifer Tsang, Science Communication and Marketing Coordinator at Addgene, is here with some tips for creating successful primers. For the full text protocol, visit www.addgene.org/protocols/pri...
Oligonucleotide primers are necessary when running a PCR reaction. One needs to design primers that are complementary to the template region of DNA. They are synthesized chemically by joining nucleotides together. One must selectively block and unblock repeatedly the reactive groups on a nucleotide when adding a nucleotide one at a time. The main property of primers is that they must correspond to sequences on the template molecule (must be complementary to template strand). However, primers do not need to correspond to the template strand completely; it is essential, however, that the 3’ end of the primer corresponds completely to the template DNA strand so elongation can proceed. Usually a guanine or cytosine is used at the 3’ end, and the 5’ end of the primer usually has stretches of several nucleotides. Also, both of the 3’ ends of the hybridized primers must point toward one another.
___________________________________________________________________________
Chapters:
0:00 Introduction to Primer Design
0:57 Primer Length
1:26 Annealing & Melting Temperatures
2:27 Makeup of Nucleotides in the Primer
3:20 Secondary Structure
4:04 You Just Designed a Primer!
___________________________________________________________________________
Credits
Featuring: Jennifer Tsang
Shot by: Jennifer Tsang
Written by: Jennifer Tsang & Quintin Marcelino
Directed, Animated, & Edited by: Quintin Marcelino
Music by: Lauren Duski, Vibe Mountain, & RKCV

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16 июл 2024

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Комментарии : 110   
@addgene
@addgene Год назад
Addgene does not regularly monitor comments posted here, so we may not see your question immediately. We’d be happy to answer any questions sent to help@addgene.org as soon as possible. Please include the name of the video along with any questions so our support team can help. Thanks!
@Nini010
@Nini010 Год назад
I like the way you explained everything with total calm and understanding, keep going and thank you❤
@yvius3265
@yvius3265 3 года назад
Thank you so much for this video! It's very helpful and explains the primers very well. And it'll surely help for my biotechnology exam next week^^
@cansudeniztozkoparan1150
@cansudeniztozkoparan1150 2 года назад
Thank you very much! It is well-explained!! I never figured out the basic PCR design until I looked at you! You're awesome!! :)
@bakhtiyorsheraliev3421
@bakhtiyorsheraliev3421 3 года назад
Wonderful explanation! I hope you keep update.
@ramkomusique
@ramkomusique 2 года назад
Thanks! This is a super neat introductory video for primer design :)
@shreyaagarwal5808
@shreyaagarwal5808 3 года назад
Complete information in the most simplified manner
@adamquazar1591
@adamquazar1591 Год назад
Thank you, Miss Ma'am! I love this video of yours, so comprehensive!
@samar7612
@samar7612 Год назад
Thank you sm. They just explained this to us in class and I didn't understand anything until I watched your video.
@carlydelsack4101
@carlydelsack4101 2 года назад
helps a bunch!!! very concise and clear!
@TransportRoutine
@TransportRoutine 3 года назад
Very informative and well-explained!!
@fayrouzashraf8233
@fayrouzashraf8233 3 года назад
This is so simple way !! Thank you♥️♥️♥️
@bradhilton2283
@bradhilton2283 2 года назад
Thanks Jennifer , That was both interesting and informative .
@ddkisa944
@ddkisa944 Год назад
Omg, this is gold. Thank you so much:)
@caveman13801
@caveman13801 2 года назад
Thanks for this video! i gotta design primers for my project and this has helped me so much :))
@Leila-ui2ci
@Leila-ui2ci 3 года назад
thanks it was really clear and helpful !!
@HaloBro003
@HaloBro003 3 года назад
This has been really helpful, thank you so much!
@shahasadsalam9757
@shahasadsalam9757 3 года назад
Simple and easy to learn...thanks
@Nw-zh1uq
@Nw-zh1uq Год назад
Thank you very much. I appreciate this video.
@SP-je5rj
@SP-je5rj Год назад
Thank you so much for this video.. it's very easy to understand..
@officialperson8802
@officialperson8802 Год назад
4:04 put smile on my face :)
@ruthzafar7272
@ruthzafar7272 3 года назад
GOOD LECTURE 👍GOD BLESS YOU TEACHER 😊
@leninehle6976
@leninehle6976 Год назад
Thank you for this video! Very well-explained (:
@bantayehubekele4111
@bantayehubekele4111 2 года назад
Very clear and informative
@ziiggybbe9116
@ziiggybbe9116 2 года назад
Thank you Jennifer
@zeamays6479
@zeamays6479 Год назад
Thank u so much.. its so informative. Love it
@ayndas.2322
@ayndas.2322 2 года назад
Wow! Such a helpful video
@km2052
@km2052 3 года назад
great explanation , thanks
@nuratikah4417
@nuratikah4417 3 года назад
Lovely Information! Thanks a lot!
@ashwinnair4816
@ashwinnair4816 4 года назад
nice.pretty good info,thanks
@anyijukamark8257
@anyijukamark8257 2 года назад
Very helpful video, thank you teacher
@sylvia7592
@sylvia7592 Год назад
thank to you now i understand the basic,
@Sanariyadlier
@Sanariyadlier 3 года назад
the content was great and so you were so sweet love it
@pratikangadi5728
@pratikangadi5728 3 года назад
Thank you very much.
@fabianaparedes124
@fabianaparedes124 Год назад
Thank you! So caring
@zaccomusic
@zaccomusic 4 года назад
good contents hope you keep update :)
@iraqi3612
@iraqi3612 2 года назад
Thank you doctor
@neetankumar4449
@neetankumar4449 Год назад
honestly so helpfullll
@user-jd4lk3rr1q
@user-jd4lk3rr1q Год назад
Best explanation!
@monimakarmacharya6472
@monimakarmacharya6472 2 года назад
Thank you so much it really helped a lot. I have my genetic engineering exams in few days. 😇😇😇✊🏻✊🏻
@anns8370
@anns8370 3 года назад
I did that lil dance at the end with you 💃✨
@chemtable7465
@chemtable7465 3 года назад
Thank you for the video
@omdah070
@omdah070 2 года назад
My advice for y’all guys always use softwares when designing your primer will save you more time and much efficient .
@carlydelsack4101
@carlydelsack4101 2 года назад
what software do u use?
@profiliomongjam1556
@profiliomongjam1556 3 года назад
Thanks for your video
@busratanl309
@busratanl309 11 месяцев назад
Very clear thank u ❣️
@kf2606
@kf2606 3 года назад
Well done!
@gracefilledatuh7029
@gracefilledatuh7029 3 года назад
Thanks so much
@vix200
@vix200 3 года назад
So pretty ❤️❤️
@Divamedina
@Divamedina 3 года назад
Amazing!!!!!!
@Liltayb
@Liltayb 3 года назад
Awesome!
@a.s9509
@a.s9509 Год назад
What are the online tools to warn us of potential hairpins, self-dimers, and cross-dimers?
@brandonherron4589
@brandonherron4589 3 года назад
Hi. Thanks for the video. :)
@mousumisau7461
@mousumisau7461 6 месяцев назад
Oh your happiness at the end😁🤗
@rashikasingh7607
@rashikasingh7607 3 года назад
Nicely eXplained
@solmazshirjang8827
@solmazshirjang8827 Год назад
It would be great if you could make a video about CRISPR KI... There is very little information available about this technique.
@Tepmodify
@Tepmodify Год назад
Good video
@user-en5xt5uu2v
@user-en5xt5uu2v 3 года назад
Thanks ❤️❤️
@saurabhtripathi1208
@saurabhtripathi1208 3 года назад
Very nice 👍
@krishnendukundu6446
@krishnendukundu6446 3 года назад
Very helpful vdo
@shatilashahi400
@shatilashahi400 2 года назад
Thanks. You speculated me with a standard presentation. I have one question if you don't mind. You said to add 4 degree for each pyrimidine base and 2 degree for each purine base to calculate melting temperature of the primer. Can you explain why I should add 4 or 2 in those perticular cases?
@klepto1840
@klepto1840 2 года назад
She explained later in the video, that C-G base pairs have 3 hydrogen bonds, while A-T pairs have just 2, therefore G-C interactions are stronger than A-T. hence the higher temperature required to melt G-C compared to A-T
@matinamatloobi9647
@matinamatloobi9647 2 года назад
tnx a lot
@franklinaladi4788
@franklinaladi4788 3 года назад
helpful! and I like the background song/beats
@ab.verykurniawan3101
@ab.verykurniawan3101 2 года назад
Great👍
@susandoming5447
@susandoming5447 Год назад
What if you don’t know the DNA sequence? How do you choose primer?
@user-bm1gy2oz6r
@user-bm1gy2oz6r 2 года назад
Super ❣️
@Just.for.fun.376
@Just.for.fun.376 2 года назад
in case of primer dimer / hairpin structure formation is there any trouble shooting method I can use , during primer design? I tried to design primer for a genomic sequence but could not avoid dimer formation. Please make a video regarding this.
@addgene
@addgene 2 года назад
Thank you for your question! You can avoid primer dimer formation by ensuring that there are no complementary sequences in your forward and reverse primers, and you can avoid primer hairpin formation by ensuring that you do not have 3 or more bases within the primer that complement each other. You can check for this when designing your primers by using primer design software such as OligoCalc (biotools.nubic.northwestern.edu/OligoCalc.html) or Primer3 (primer3.ut.ee/), which can check for self-complementarity in your primer pairs. I hope this information helps.
@zienanema4691
@zienanema4691 3 года назад
Very beautiful
@jeffersonselikemnyame9516
@jeffersonselikemnyame9516 3 года назад
how do we find the tools to identify dimers and cross dimers?
@addgene
@addgene 3 года назад
Here's a link to a good resource that should help you with that: www.idtdna.com/pages/tools/oligoanalyzer
@Emusic1621
@Emusic1621 3 года назад
I have the protocols for normal PCR.how can I optimize them for using multiplex PCR
@addgene
@addgene 3 года назад
These publications should be helpful :) pubmed.ncbi.nlm.nih.gov/9298224/ www.sciencedirect.com/science/article/pii/B9780123721853500079 PubMedPubMed
@ukkytoo
@ukkytoo 2 года назад
Please tell me what are the reasons for the annealing temperature to be lower than the melting temperature by 5 degrees?
@addgene
@addgene 2 года назад
Thanks for the question! An annealing temperature 5C below the Tm can be used as starting point for PCR, but this temperature is something that may need to be optimized for high yields. A temperature of 5C below the Tm should allow for annealing to the expected target site. Lowering the annealing temperature further though could increase annealing to off target sites that differ by single nucleotide mismatches.
@ethanhilgert3995
@ethanhilgert3995 3 года назад
I am definitely no longer amongst my reloading brothers. I’m lost
@JOSIPPOGI
@JOSIPPOGI 2 года назад
Question when making primers do you make them in a random order
@addgene
@addgene 2 года назад
Hello, thanks for your question! The primer sequence is based on the template sequence (displayed in blue in the video). If that didn't quite answer your question, we suggest checking out Sigma Alrich's page on oligonucleotide synthesis, that may be of some help. www.sigmaaldrich.com/US/en/technical-documents/technical-article/genomics/pcr/dna-oligonucleotide-synthesis
@Senshidayo
@Senshidayo 2 года назад
I don’t know why I saw this but Jennifer is cute lol. And I learned something.
@eup2309
@eup2309 2 года назад
pretty lady, pretty explanations.
@mouniaakassou806
@mouniaakassou806 4 года назад
Could please explain ddPCR vs PCR. Thanks
@addgene
@addgene 4 года назад
Thanks for the question! ddPCR first separates your reaction into thousands of individual droplet where each droplet is an individual PCR reaction. You can read more about it in the "AAV titering using droplet digital PCR" section of this blog post: blog.addgene.org/droplet-digital-pcr-for-aav-quantitation , or check out this page for morewww.bio-rad.com/en-us/applications-technologies/digital-pcr-real-time-pcr-qpcr-choices-for-different-applications?ID=OENHBB15
@mouniaakassou806
@mouniaakassou806 4 года назад
@@addgene thanks a lot
@saratpiyaniran7705
@saratpiyaniran7705 4 месяца назад
👍🏻👍🏻👍🏻
@Stronger.119
@Stronger.119 2 года назад
How to upload the synthetic gene on the plasmids
@addgene
@addgene 2 года назад
Hello, and thanks for the question. We're not exactly sure what you're specifically referring to, but if you have any questions, you can contact help@addgene.org and our science support staff can assist you.
@BearMeat4Dinner
@BearMeat4Dinner Год назад
I love the shirt and great video! :D
@martintraseas7514
@martintraseas7514 2 года назад
Todays exam studied🙏🏽😊
@travelthailand885
@travelthailand885 2 года назад
if we already get our design in software. how do we get the real one?
@addgene
@addgene 2 года назад
There are several companies that synthesize primers. We recommend viewing Sigma Alrich's website on oligonucleotide synthesis. Using solid-phase chemical synthesis, each nucleotide is added on the 3' end. www.sigmaaldrich.com/US/en/technical-documents/technical-article/genomics/pcr/dna-oligonucleotide-synthesis
@anupam7130
@anupam7130 3 года назад
Nice genes...
@jpcapobianco1979
@jpcapobianco1979 2 года назад
can i ask a question ? if you can't isolate a virus how can you design a primer for pcr ? you simply invent it ?
@addgene
@addgene Год назад
Thank you for your question. As long as you know the genomic sequence of the virus you are interested in, you can design a primer for that virus following the same tips and guidelines described in this video. You can also check out Sigma Aldrich’s page on PCR assay design for more information: www.sigmaaldrich.com/US/en/technical-documents/protocol/genomics/pcr/pcr-qpcr-dpcr-assay-design
@prajwalpurushottamdongare3582
@prajwalpurushottamdongare3582 2 года назад
can u answer the doubts in chat?
@premprem749
@premprem749 Год назад
प्रेम
@SixelaAM
@SixelaAM 2 года назад
why 4° and 2°C for the Tm ? :(
@addgene
@addgene 2 года назад
Thanks for the question! An AT base pair has two hydrogen bonds, while a GC base pair has 3 hydrogen bonds so a higher temperature (4 C) is required to break a GC base pair, relative to an AT base pair (2 C).
@SixelaAM
@SixelaAM 2 года назад
@@addgene thank you, you saved me!
@ishashukla1394
@ishashukla1394 2 года назад
But primer are RNA segment not DNA.
@cristobalurrutia7683
@cristobalurrutia7683 2 года назад
They're DNA oligonucleotides, not RNA
@cnsisow
@cnsisow 3 года назад
It bothers me how she keeps reading from the teleprompter.
@felipevilicich980
@felipevilicich980 3 года назад
No one cares about your opinion bro
@cnsisow
@cnsisow 3 года назад
@@felipevilicich980 reported for hate speech
@abtintari153
@abtintari153 3 года назад
@@cnsisow he called you bro. sounds more like a love speech to me !
@drakbarpk
@drakbarpk 3 года назад
@@cnsisow lmao how is them not caring about u hate speech
@muhammedikram350
@muhammedikram350 2 года назад
Very informative and interesting
@user-on3wo7en8c
@user-on3wo7en8c 2 года назад
👍🏻👍🏻👍🏻
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