...previous posts for our Plasmids 101 series, we examined a number of important plasmid elements – promoters...circular piece of DNA (and is not maintained).  Translocation: If the sites are on separate DNA molecules, ...Resources on Addgene.org Find Cre plasmids Find loxP plasmids  ...for creating (excuse the pun) specific, targeted DNA modifications in transgenic animals, embryonic stem...inserting loxP sites at deliberate locations in a DNA sequence allows for very specific manipulations as...located either on the same or on separate pieces of DNA. Both 13bp repeat sequences on a single loxP site...Cre proteins to form a tetramer. A double-strand DNA break occurs within the core spacer of each loxP ...

...Browse our Plasmids 101 blog posts Read blog posts on plasmid cloning Read about different plasmid elements...or PCR conditions. Purifying DNA fragments Once you’ve generated your DNA fragments, it is always a good...amount of DNA. As a general rule, try to use an excess of insert compared to the backbone plasmid; a starting...mistake or a mistake by the DNA analysis software. Now that you've read our plasmid troubleshooting guide, ...colonies screened might not contain the correct plasmid. There’s a lot that can go wrong! With all the ...cloning project, and hopefully obtain your coveted plasmid with no substantial delays. Design, design, design...spend some time outlining the construction of the plasmid and all the steps you will have to take. Decide...

...of the new plasmids, antibodies, and viral preps in our repository through our Hot Plasmids articles. ...landing sites on opposite DNA strands. When the prime editor releases the DNA, the two 3’ flaps containing...be used for applications beyond cryo-EM.   Find plasmids for MagIC-Cryo-EM here!   Arimura, Y., Konishi...disease phenotype in an animal model. Find PE-eVLP plasmids here! The lab’s other recent deposit builds on...previously-reported technique for precisely integrating large DNA sequences into a genome (Anzalone et al., 2022). ...prime editing and twin prime editing can integrate DNA cargoes of 80–100 bp, PASSIGE can integrate cargoes...over the wild-type enzyme. Find optimized PASSIGE plasmids here!     Figure 3: Schematic of the PASSIGE...

...cells to retain plasmids - if a cell does not inherit plasmid due to improper plasmid partitioning, it...found that if a mini-F plasmid carried a specific 700 bp segment of DNA, the plasmid was propagated better...unstabilized plasmids were retained in less than 10% of cells while plasmids containing the plasmid addiction...death. In the case of plasmids, toxin-antitoxin systems act as “selfish” pieces of DNA whose sole purpose...ensure that plasmids are passed down through generations (Figure 1). These so called “plasmid addiction ...only survive if they retain the plasmid. Since their discovery, plasmid addiction systems have been used...better than plasmids without this DNA. They eventually designated this fragment as the ccdB region (for “...

...containing those overhangs. Entry DNA overhangs may be present in the original plasmid (Option 1) or added using...that flank their DNA fragment in an inverse orientation. This allows for multiple DNA components (promoters...assembly of multiple DNA fragments to create TAL effector nucleases. These plasmids were designed to utilize...Addgene’s plasmids are used with a wide variety of restriction enzyme-based cloning methods. Each method...sequence, they can be customized to direct assembly of DNA fragments. When designed correctly, the recognition...assembly require 20-40 bp of homology at the ends of DNA fragments to specify assembly order, so fragments... and BpiI/BbsI to efficiently assemble up to six DNA fragments at a time. As with all Golden Gate-based...

...subset of the new plasmids and viral preps in the repository through our hot plasmids articles. These articles...recent plasmid deposits and we hope they'll make it easier for you to find and use the plasmids you need...to contemplate DNA in terms of its sequencing, in vivo studies should always take DNA’s chromatin status... probes target chromatin to visualize DNA, an editor targets DNA (via catalytically inactive dCas9) to...highlights from recent CRISPR plasmids. To find all of the CRISPR plasmids available from Addgene, head...head over to our CRISPR Plasmids and Resources page.  Plasmids for delivering CRISPRi components by a single...inducible degron system for C. elegans New CRISPR plasmids New items from the viral service Epigenetic ...

...lentiviral plasmids include popular envelope and packaging plasmids as well as transfer plasmids. Download...Otherwise, check out our plasmid and DNA backgrounds. Download the blue plasmid background.     You can...the green DNA background.     Since we ❤️ DNA at Addgene, we're presenting you with another DNA background... the plasmids that Addgene offers by visiting our collections page. Here, you can browse plasmids by field...your favorite reagent, scientific technique, or plasmid repository at your next meeting.     If you’re...cute mascots!  Blugene has been helping us make Plasmids 101 videos and needed a break so they're hanging...coronavirus collection page, where you can find plasmid tools to accelerate your COVID-19 research.  Download...

... of DNA through error-prone non-homologous end joining (NHEJ). In targeted DNA knock-in, donor DNA is ...genomes. Such protein-DNA structures presumably reduce the likelihood that donor DNA will interact with ... donor DNA Adenoviral CRISPR/Cas9 genome editing tools can also be used to deliver Cas9 and DNA templates...Gonçalves and Ventura labs’ plasmids, including protocols, check out the plasmids at Addgene: pAdSh.PGK.Cas9...looking for a broader range of CRISPRs plasmid tools, find more plasmids, CRISPR technology guides, FAQs, and...viruses. Adenoviruses are non-enveloped double-strand DNA viruses with a genome of around 36 kb in size, which...Schematic of targeted gene knock-out (left) and targeted DNA knock-in (right) by CRISPR/Cas9. Adenoviral CRISPR...

...sharing plasmids through Addgene is that we provide an added level of confidence in the plasmids we distribute...ensuring plasmid quality is to stay organized. Here at Addgene, we collect data on every plasmid we distribute...location of every plasmid in your collection. Use one of the many freely-available DNA-editing software...cloned into the plasmid) and any other important features that differentiate this plasmid from its predecessor...sequence analysis, plasmid verification, and using NCBI BLAST. Tips for high-throughput plasmid sequencing If...Analyzing and Troubleshooting DNA Sequence Learn Additional Ways to Verify Your Plasmid Learn How Addgene Uses...on the Addgene Website View our Plasmid Reference Pages Get Plasmid Backbone Information from Our Vector...

...bind to a specific DNA sequence via a targeting gRNA. But dCas9 does not cleave the DNA. Much of the research...recognition sequence into the genomic DNA that could then be recognized by a DNA-binding molecule (Hoshino and...chromatin or library of purified DNA for purification of a specific chromatin or DNA fragment (Fujita et al., ... tag expressed on a plasmid, allowing for in vivo biotinylation through a plasmid-based biotin ligase....CRISPR guide Find CRISPR plasmids by function Find recently deposited plasmids ...and Fujii, 2013). They call this method engineered DNA-binding molecule-mediated chromatin immunoprecipitation...immunoprecipitation (enChIP) because any engineered DNA-binding molecule, such as Zinc-finger or TAL proteins, can...

...single base changes in the DNA sequence without completely cutting the DNA. RNA Editors: CRISPR nucleases...Interspaced Short Palindromic Repeats: Sequences of DNA found in bacteria that allow the bacteria to target...bacterial immune system. Genome Editing: Modifying the DNA sequence of an organism’s genome usually for a research...of RNA that direct the CRISPR system to cut other DNA or RNA sequences. Nucleases: Proteins that bind... and are directed by the gRNAs to cut particular DNA or RNA sequences. Cas9 is a very commonly used CRISPR...CRISPR nuclease. Note: Most CRISPR plasmids from Addgene produce either a gRNA, a nuclease, or both....Applications of CRISPR: Cut: CRISPR can be used to cut the DNA sequence. With a repair template, CRISPR can be used...

... to cleave DNA outside of the recognition sequence. This requires that the vectors and DNA fragments contain...developed and fine tuned many different ways to clone DNA fragments which have provided appealing alternatives...scientists are using Gibson assembly to put together DNA fragments. As a fun way to start, I highly recommend...known for allowing easy assembly of multiple linear DNA fragments, but can also be used in basic cloning ... in the figure below. To start, you need to have DNA fragments with regions of homology at their ends,...homology to anneal a polymerase, to fill in the gaps a DNA ligase, to seal the nicks of the annealed and filled-in...can be purchased from a company (e.g. NEB or SGI-DNA), or can be mixed yourself (e.g. see the Miller Lab...

...in molecular biology is DNA→RNA→Protein. To synthesize a particular protein DNA must first be transcribed...and used to manipulate DNA), or in medicine (e.g. insulin). Proteins, unlike DNA which can be relatively... is quite simple; DNA coding for your protein of interest is inserted into a plasmid expression vector...modifications Learn more molecular biology in our Plasmids 101 eBook! Researchers use various techniques ...expression consists of transfecting cells with your DNA template of choice and allowing these cells to transcribe... modifications for proper protein function. Most DNA constructs designed for mammalian expression utilize...from the cellular debris. There are several popular DNA vectors that can be used to produce large amounts...

... used for plasmid-based experiments. What are control plasmids? Generally, control plasmids help to ensure...follow an example of a plasmid-based experiment, delineate its requisite control plasmids, and discuss why ... shRNA target correct? Is the purified plasmid DNA viable? Or cytotoxic? How and where did things go wrong...proper control plasmids would address and answer these questions. Types of control plasmids Part of planning... experimental conditions, including how much plasmid DNA to use for any individual or co- transfection...conditions and plasmids should produce a null effect (i.e., no phenomenon is observed). In any plasmid-based experiment... are conducive to the successful delivery of plasmid DNA into the cells, the internal control vector then...

...highlight a subset of the new plasmids in the repository through our hot plasmids articles. These articles ...recent plasmid deposits and we hope they'll make it easier for you to find and use the plasmids you need... as a DNA staining dye Article contributed by Jennifer Tsang Figure 4: Double stranded DNA bound... fusions with tTALE to “stain” DNA. TALE proteins can bind specific DNA sequences which brings the attached...attached fluorescent protein to the DNA. They created plasmids for purification of tTALE-eGFP and tTALE-mCherry...need. If you'd ever like to write about a recent plasmid deposit please sign up here.  Human whole genome...alternative to intercalating fluorescent dyes for DNA-protein interaction studies? Kyubong Jo's lab generated...

...that acts as a DNA gyrase poison, locking up DNA gyrase with broken double stranded DNA and ultimately...Addgene Blog Plasmids 101: Common Lab E. coli Strains Plasmids 101: TOPO Cloning Plasmids 101: Golden ...-containing vectors in mind, any plasmid that contains the F plasmid (F’ strains) will also be resistant...Bernard, P., et al. “The F plasmid CcdB protein induces efficient ATP-dependent DNA cleavage by gyrase.” J..., M. “Cell killing by the F plasmid CcdB protein involves poisoning of DNA-topoisomerase II complexes....... The ccdB gene, located on the F sex factor plasmid of E. coli, is part of a toxin-antitoxin system...encoded by the ccd operon, which is responsible for plasmid maintenance during cell division. ccdB codes for...

...crRNA DNA 5' NGG Specific blunt ended DSB in target DNA Cpf1 RuvC-like crRNA DNA 5' TTN Specific...virus, genotype human DNA, identify tumor mutations within cell-free genomic DNA, and detect COVID-19 ...require both a tracrRNA and crRNA to cleave target DNA (Cpf1 requires only a crRNA for target recognition...is that Cas13a binds and cleaves RNA rather than DNA substrates. In terms of structure, Cas13a shares ... Cas9 uses HNH and RuvC domains to cleave target DNA. The HEPN domains within Cas13a are essential for... Specific DSB in target DNA with 5' overhangs Cas13a (C2c2) 2x HEPN crRNA RNA 3' A, U, or C (not required...crRNA to facilitate binding and cleavage of target DNA respectively. LshCas13a, on the other hand, uses ...

... our high-throughput DNA isolation process that yields high-quality isolated DNA samples of sufficient...every isolated plasmid sample and normalize each to fall within a 10 fold range. Plasmids that don't meet...A broader view of the whole plasmid To confirm the sequence of the plasmid, we examine three things: ...expected and do not affect plasmid function, we will update information on the plasmid’s page. Sometimes we’re...’re missing a piece of the plasmid There are regions of some plasmids that are particularly difficult ...some plasmids will not result in one complete, circular assembly. Most of the time, these plasmids are ...bottom of the plasmid page. Viral preps and pooled libraries In addition to regular plasmid sequencing,...

... addition to Taq DNA polymerase, PCR requires free nucleotides (dNTPs), template DNA to amplify from and...unique single stranded DNA primers that bind upstream (5’) and downstream (3’) of the DNA region of interest...crucial for this process as DNA polymerases require an existing strand of DNA to add nucleotides to.  Using...reaction:  Denaturation- To amplify DNA, the two strands of the template DNA first have to be separated. This...primers can anneal to the single stranded DNA template strands. DNA polymerase is also stable at this temperature...specific target of DNA. This amplicon can be used in molecular cloning to create a plasmid of interest, for... of amplified DNA of a known starting concentration. The cycle in which the unknown DNA is detected compared...

... and extract plasmid DNA directly from the colonies. Transform the resultant plasmid DNA into E. coli ... cloning phage DNA can be difficult, in part because phages frequently alter their DNA by adding methyl...fragment library of phage DNA This first step involves digesting phage genomic DNA into 1-3 kb (approximately...involves forcing DNA through a small opening using compressed nitrogen gas; this shears DNA at random locations...If working with DNA that is refractory to enzymatic manipulation, amplifying phage DNA with phi29 polymerase...certain modifications to DNA bases.  Ligate and transform your resultant plasmid libraries into chemically...Step 2: Express random phage DNA fragments in E. coli Now that random DNA fragments have been cloned into...

...organization scheme for multi-part DNA assembly. Simply put, it assembles individual DNA components into larger units...As a plasmid repository, we are no strangers to cloning. If you’re reading this, then chances are you...enzyme and a ligase are used to assemble multiple DNA fragments together in a one-tube reaction. Even though... down into three hierarchical levels: individual DNA parts, transcriptional units, and multigene constructs...transcriptional units. Individual parts are defined DNA sequences with specific functions. Most individual...proteins which interact with other proteins and with DNA, and these complexes regulate the transcription of...systems whose protein products can interact with the DNA that encodes the protein itself or other genes within...

...features was our collection of popular plasmid sequences. These plasmids contain features such as antibiotic...sequence match even when the DNA sequence has changed. Identifying plasmid control elements Coding sequence... our SnapGene powered plasmid maps Learn how we use SnapGene during the plasmid quality control process...out full plasmid sequencing at Addgene Additional Resources on Addgene.org Example plasmid analysis ...available to biomedical researchers manipulating DNA sequences on a daily basis, many found these tools...design was done painstakingly by hand. Records of plasmid construction were often incomplete or nonexistent...know the complete sequences or properties of the DNA molecules they were using. SnapGene was created ...

...ambiguous that the DNA sequencing reaction should be repeated. Guidelines to help with DNA sequencing troubleshooting... sequences! More DNA Sequencing Resources: Tips for Using BLAST to Verify Plasmids Acknowledgements...on BitesizeBio here. As part of my job ensuring plasmid quality at Addgene, I analyze 50-100 sequencing...gel you always include proper controls like uncut DNA and the proper ladder. These controls help you properly...your favorite sequencing facility. When it comes to DNA sequencing the chromatogram is your visual control...the rescue for analyzing and troubleshooting your DNA sequencing results Above (top right corner of this...this post) is an example of a seemingly clean DNA sequence (no Ns in sight). If you never looked at the...

...viral vectors and plasmids with repeating sequences. Repeating sequences within a plasmid can undergo intramolecular...contain the full length plasmid.   Figure 1: The full lentiviral plasmid is expected to be >12 kb...in my samples? Plasmid recombination can affect viral vectors (LTRs and ITRs), plasmids with multiple ...other plasmids that contain repeating elements. Knowing how to amplify recombination-prone plasmids and ... length plasmid. If you find that your bacterial cultures contain a mix of full length plasmid and the...smaller, recombined plasmid around 1.5 kb. When cut with BamHI, the expected linear plasmid is present, but...but the recombined plasmid is still visible. This indicates that the DNA prep contains a mixture of the...

...molecular biologists use to tinker with DNA. Making changes to a DNA sequence can help scientists identify...specific mutations in your plasmids Use REPLACER Mutagenesis to mutate your plasmid Resources on Addgene.... is used to direct the PolI3M-nCas9 complex to a DNA site of interest, which nCas9 nicks and then dissociates...dissociates from. PolI3M then binds the nicked DNA, and extends it from the 3’ end, while its native endonuclease...to a site of interest, where it nicks its target DNA (left). Cas9 dissociates and PolI binds (middle) ...increasing the standard mutation rate seen during DNA replication by 120-fold over background. Due to its... These changes promote nCas9’s dissociation from DNA after nicking and yielded an enhance nCas9 (enCas9...

...restriction enzyme such as BsaI, and a DNA ligase such as T4 DNA ligase. Inserts, either precloned or in...completion of T4 DNA Ligase fidelity studies conducted by Potapov et al. at NEB (1, 2). While T4 DNA Ligase, the... comprehensive profiling of T4 DNA ligase fidelity and bias during DNA end-joining." Nucleic acids research... Gate Assembly is commonly used to assemble 2–10 DNA fragments in a single “one-pot” reaction to form ...junction sequences guided by experimentally-derived DNA Ligase fidelity data. Our work demonstrates that ...antibiotic selectable markers by the destination plasmid. Antibiotic selection allowed for high throughput...accurate assemblies was achieved by the sequencing of plasmids isolated from blue or white colonies. Sequencing...

...recombined plasmid to overtake full-size plasmids (or for smaller plasmids to overtake larger plasmids, if the...How many unique plasmids does your library contain?), the variance of size of plasmids in your library...Library. DNA and cell amounts After deciding on a cell type, you will need to determine how much DNA and how...electroporator uses, etc. The DNA amount can be anywhere from 10 ng to 1 μg of DNA. It often correlates with...Library Type Name Number of Plasmids Variable Region Size DNA per Amplification Amplification...lead to issues such as recombination and loss of plasmid diversity, so Addgene strives to distribute aliquots...library (How important is it that every single plasmid in your library is present, and how will you ensure...

...you can either order a DNA pooled library, which contains a collection of plasmids in a single tube, or ...Transfection of the DNA pooled library and appropriate packaging and envelope plasmids into HEK cells allows...similar to amplifying a plasmid: transform E. coli with the pooled library DNA, allow the bacteria to ...single plasmid transformation, though, a pooled library has hundreds to millions of distinct plasmids, all...anyone who has worked with individual plasmids knows, some plasmids amplify well and others don’t. The size...library. Addgene’s pooled libraries are typically DNA preps, but we do distribute several of our most popular... prepare the libraries for you.  Starting from plasmids requires amplification, verification, and lentiviral...

...resistance DNA plasmids are traditionally grown in bacteria as a way to produce more of the plasmid, isolate...isolate individual plasmids, or express a gene contained in a plasmid. During the propagation and/or transformation...receive a copy of the plasmid or will lose it during division. These non-plasmid-containing bacteria can...induce cell death by intercalating into DNA and generating DNA breaks. The Sh ble gene provides zeocin...meaning it will induce mutations in the host/plasmid DNA during selection if it’s not completely bound...: Doesn’t work for all bacteria; may cause plasmid/host DNA damage. Choosing an antibiotic resistance ...Over-Agar Antibiotic Plating Plasmids 101 eBook Resources on the Addgene blog Plasmids 101: Antibiotic Resistance...

...enChIP Plasmids? All Hodaka Fujii lab plasmids Sign up to receive email alerts when new plasmids from ...engineered DNA-binding molecules for the first time and named the new technology as engineered DNA-binding... shopping for a wide range of plasmids. The merit of depositing plasmids to Addgene has been spectacular...chromatin immunoprecipitation (iChIP) and engineered DNA-binding molecule-mediated chromatin immunoprecipitation...insertion of recognition sequences of an exogenous DNA-binding protein such as LexA into the target locus...which is the rate-limiting step. When engineered DNA-binding molecule technologies such as TAL proteins... it struck me that direct use of such engineered DNA-binding molecules even enables us to skip the step...

....org Find Cre-Lox Plasmids Find Optogenetics Plasmids Find Chemogenetics Plasmids ...Saccharomyces Cerevisiae 2 Micron Plasmid Attaches Covalently to DNA via a Phosphotyrosyl Linkage.” Molecular...specific (and often cell type specific) control of DNA recombination and gene expression can be advanced...which is named after its ability to invert or ‘flip DNA’, is derived from the yeast S. cerevisiae (Gronostajski...lead to excision, inversion, and translocation of DNA in a similar fashion as between loxP sites (For details...are reversible. Whereas the excision of a piece of DNA flanked by loxP/FRT sites is favored over its reintroduction...the same probability. Continuous inversion of the DNA sequence of interest can lead to poor expression ...

...cuts genomic DNA. The interplay between Cas9 (which causes the breaks) and host cell DNA repair factors...investigations into the release of DNA post-cut. Using substrate DNA labeled on both sides of the break...double stranded donor DNA with other design parameters. Example single stranded donor DNA and a presumptive... Figure 2: Single-stranded donor DNA interaction with the Cas9-DNA duplex. Image from Richardson et al...in uncut target DNA that was accessible to anneal with complementary single stranded DNA. We thus wondered...donor DNA. Chris Richardson is a Postdoctoral Researcher in Jacob Corn’s lab investigating DNA repair...complementary ssDNA molecules in vitro. Figure 1: Cas9 binding to the cleaved DNA duplex. Image...

...Cascade binding and subsequent DNA degradation appears to be conserved. This DNA degradation portion can be...Most Cas effectors have one job — Cas see DNA, Cas chop DNA. Cas3, however, has two jobs, one as a nuclease... kilobases down the strand of DNA, Cascade caught up to it, and then DNA degradation continued. However...and Cas3 begins unraveling the double-stranded DNA (dsDNA) in what is called a reeling mechanism (see next...for details). The newly formed single-stranded DNA (ssDNA) is then pulled through Cas3. After these initial...continually passing the ssDNA past the nuclease domain, Cas3 is able to repeatedly cut the DNA at an efficient...The versatility of CRISPR allows you to play with DNA in a number of ways, from small edits that change...

...the ability to distribute plasmids with the piggyBac™ transposon. These plasmids, when combined with a source... genome fully intact, while, with a standard DNA plasmid transfection, a double-stranded break may occur...utilizing a piggyBac™ transposon in a donor plasmid carrying the DNA edit of interest, along with a site-specific...CRISPR/Cas9) to create a double-stranded DNA break. After DNA cleavage, the piggyBac™ donor is used by...efficiency over transfecting with plasmids in some cell lines, most likely due to DNA toxicity. More importantly...licensed distributor) allow you to quickly transfer a DNA sequence from the transposon vector to one of many...useful resource. While Addgene cannot distribute plasmids with the piggyBac™ transposase itself, please ...

...trained on Addgene plasmid datasets) to predict the lab-of-origin of engineered DNA. Both of these groups...synthetic biology page Search for a plasmid Find Addgene's most popular plasmids ...been coming to the Addgene website in search of plasmids. Now, scientists are beginning to see Addgene ...Addgene as a large data set. Addgene has over 65,000 plasmids in the repository, each verified by sequencing...data to learn about trends in synthetic biology and DNA synthesis. They published their results in a paper...Synthetic biology, in particular, the ability to do DNA synthesis, is evolving so fast that it is a really...variation in GC content between many organisms and DNA synthesis companies often work within a narrow range...

....12137. PubMed. Find the Plasmids at Addgene Kowarz Lab plasmids Izsvak Lab plasmids  ...the gene of interest (blue) in a plasmid backbone. A separate plasmid contains the transposase gene (red...occurs which cuts the DNA.3.) The released transposon can now bind a strand of DNA with a TA dinucleotide...). The original plasmid is empty following the removal of the transposon; the plasmid is then degraded...Transposons are sequences of DNA that can move around in a genome. In a laboratory setting, transposons...transposons combine the advantages of viruses and naked DNA while eliminating some of the drawbacks. Specifically...transposase creates a double strand break in the DNA and allows the tranposon to integrate. Additionally...

...nick-selective DNA ligases like Taq DNA Ligase, HiFi Taq DNA Ligase, and the ATP dependent 9°NTM DNA Ligase are...about it. DNA ligases are enzymes that seal breaks in DNA by joining 5 ́-phosphorylated DNA termini to... several DNA ligases bound to substrate (23, 24). Thermostable DNA ligases, including Taq DNA ligase, ...Blog Learn New Plasmid Cloning Techniques Pushing the Limits of DNA Assembly Plasmid Cloning by PCR ...to 3 ́-OH DNA termini (1-4). In vitro, ligases (notably T4 DNA ligase) are critical reagents for many ...temperatures (37–75 °C). T4 DNA ligase is highly active in nick ligation and DNA end-joining, but will also...gaps. For example, DNA assembly methods, such as Gibson Assembly® and NEBuilder® HiFi DNA Assembly, require...

...highlight a subset of the new plasmids in the repository through our hot plasmids articles. These articles ...recent plasmid deposits and we hope they'll make it easier for you to find and use the plasmids you need...write about a recent plasmid deposit please sign up here. Listen to the Hot Plasmids Podcast!  MarathonRT... 20 nm of a specific DNA sequence in only 1 min. Using these lentiviral plasmids, catalytically inactive...’s lab at Yale University recently deposited a plasmid for expressing a novel reverse transcriptase (RT...biology and enable the conversion of RNA templates to DNA but suffer from several important shortcomings including...). MarathonRT also faithfully transcribes RNA to DNA with low error rates compared to other RTs. MarathonRT...

...evidenced by all the CRISPR publications, press, and plasmids out there, it’s obvious that CRISPR is a ground-breaking...that Cas9 cutting efficiency increases when target DNA strand separation is stabilized (2,3). Stable strand...interactions between the groove and the negatively charged DNA and therefore destabilize basal strand separation...cutting. Figure 1: Strand separation and target DNA binding to the Cas9 nuclease. Stable strand separation...sequence independent interactions between Cas9 and DNA, then they could diminish off-target cutting (4)....between Cas9 and the phophate backbone of the target DNA strand via mutations N497A, R661A, Q695A, and Q926A...compared to eSpCas9(1.1) and SpCas9-HF1. The HypaCas9 plasmids are available from Addgene here! Future possibilities...

...target any sequence of DNA. Second, NgAgo target specificity is dictated by a DNA guide sequence rather...(2016). 3. "NgAgo: Genome-editing by a DNA-guided enzyme." DNA-scissors (blog). Blog website. 4. Hsu, ...be produced from a plasmid in cells. Additionally, in vitro assembly of NgAgo/ssDNA requires incubation...genome editing! Check Out Other Argonaute Plasmids from the Doudna Lab Many thanks to our Guest Blogger ...sequencing on select regions of all distributed plasmids as part of quality control, but does not perform...sharing the stage with much-lauded CRISPR-Cas9 is DNA-guided endonuclease NgAgo! We'll discuss how NgAgo...methods have their own pros and cons (2). The NgAgo DNA guide is inexpensive and can be 5’-phosphorylated...