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We narrowed to 159 results for: crispr grnas

Showing: 121 - 140 of 159 results
  1. Twelve Amazing Guest Blog Contributors!

    Type
    Blog Post
    Published
    Nov. 26, 2024, 2:15 p.m.
    ...about recent CRISPR deposits from Arlene Sharpe’s lab. X-Chime and Performing In Vivo CRISPR Screens Using...software that predicts efficiencies of prime editing gRNAs.   PRIDICT Harvinder Virk and Michael Biddle, ...
  2. X-CHIME: Context Dependent Germline Knockout in Immune Cells

    Type
    Blog Post
    Published
    Jan. 16, 2024, 6:13 p.m.
    ...Design Your gRNA for CRISPR Genome Editing CRISPR Cheat Sheat Resources from Addgene.org CRISPR Guide CRISPR...time-consuming, as it only changes one gene at a time. CRISPR-based systems enable gene knockout in immune cells...stem cells with a lentiviral vector containing a gRNA. These transduced stem cells can be implanted in...and in combination with different genes. Having CRISPR systems for assessing genes in defined contexts.... G., Haining, W. N., & Sharpe, A. H. (2019). A CRISPR-Cas9 delivery system for in vivo screening of genes...
  3. CASTing Off for New Shores in Human Genome Editing

    Type
    Blog Post
    Published
    June 10, 2025, 1:15 p.m.
    ...nuclease-deficient CRISPR-Cas system identifies and binds a genomic target using a gRNA, and an affiliated...Engineering Using CRISPR-Transposons Degrading DNA with Cascade-Cas3 Typing CRISPR Systems Prime Editing... Flexibility to CRISPR Editing Additional resources on Addgene.org Addgene's CRISPR Guide (Jump to Large...hardly seems like we finish writing about one dual CRISPR-transposon system before another exciting new advance...emerges! The programmability and targeting power of CRISPR combined with the large sequence capacity of transposons...arrival on the scene is called evoCAST — an evolved CRISPR-associated transposase (CAST). Back up a second...transposons captured and repurposed nuclease-deficient CRISPR-Cas systems to help them spread through bacterial...
  4. Hot Plasmids and Viral Preps - May 2021

    Type
    Blog Post
    Published
    May 18, 2021, 1:15 p.m.
    ...2021.01.30.428974   The CRISPR corner By Jennifer Tsang Here are a few highlights from recent CRISPR plasmids. To...To find all of the CRISPR plasmids available from Addgene, head over to our CRISPR Plasmids and Resources... light to deactivate photocleavable gRNAs within seconds. A CRISPR-based lineage tracing tool captures...per gene where gRNA expression is induced by anhydrous tetracycline. Three new anti-CRISPRs were identified...Nanocompartments for yeast bioproduction pathways The CRISPR corner New ready-to-use viral preps Mapping antibody...series of vectors and DNA modules for assembly of CRISPR/Cas9 constructs. zCas9i is a high efficiency intron-optimized...
  5. Hot Plasmids: February 2026

    Type
    Blog Post
    Published
    Feb. 17, 2026, 2:15 p.m.
    ...Wine and dine using CRISPR knockout libraries By Alyssa Shepard Connoisseurs of CRISPR knockout screens ...of data you can get from your CRISPR screen (Figure 5). First, the gRNAs for the Jacquere and Julianna...month, check out hot new AAV packaging plasmids, CRISPR libraries, and more! Read on to learn more about...with a single stop codon Improved mouse and human CRISPR knockout libraries Neurexin and Neuroligin antibodies...expert pairing of Jacquere and Julianna, lentiviral CRISPR knockout libraries for genome-wide screens in humans...targets for each species. Second, they use updated gRNA design models, to balance on-target activity with...variations in the tracrRNA, the structural sequence of a gRNA. The Jacquere library was tested in two human cell...
  6. PRIDICT: Predicting Efficiencies of Prime Editing Guide RNAs

    Type
    Blog Post
    Published
    June 25, 2024, 1:15 p.m.
    ...Design Your gRNA for CRISPR Genome Editing PRIME Editing: Adding Precision and Flexibility to CRISPR Editing...Resources on Addgene.org CRISPR: PRIME Edit Collection The CRISPR Guide Empty gRNA Expression Vectors...models. In addition, we provide options for nicking gRNAs (used for PE3 and PE5 prime editing strategies) ...
  7. 15 Hot Plasmids from 2017

    Type
    Blog Post
    Published
    Jan. 9, 2018, 3:02 p.m.
    ...to increase CRISPR editing efficiency across multiple CRISPR enzymes. Plasmids for CRISPR coselection ...podcast segment on CRISPR tools for plants CRISPR inhibitors Bacteria utilize CRISPR Cas9 systems to defend...on Coselection with Ouabain New CRISPR base editors The popular CRISPR base editing technique uses dCas9...back using CRISPR inhibitors. Several such inhibitors have been characterized for type I CRISPR systems,... et al. PLoS ONE. 2017. PubMed PMID: 28241009 CRISPR coselection with ouabain increases editing efficiency...Doyon’s lab has developed a new method to increase CRISPR editing efficiency in mammalian cells. Their marker-free..., ouabain selection enriches the population for CRISPR edits and improves editing efficiency. Importantly...
  8. Plasmids 101: Modular Cloning

    Type
    Blog Post
    Published
    March 12, 2024, 1:15 p.m.
    ...variables all at once. CRISPR CRISPR arrays and libraries depend on many gRNAs delivered with a relevant...nuclease. MoClo can be used to assemble multiplexed gRNA systems as well as additional components such as...etc. MoClo is especially useful for more complex CRISPR experiments (e.g., many guides/parts delivered)...delivered) in certain model organisms. In mammals, most CRISPR libraries are assembled and delivered virally, ...
  9. Cutting Once Is Harder Than It Sounds: Your Guide to Minimizing Off-Target Effects

    Type
    Blog Post
    Published
    March 31, 2026, 1:15 p.m.
    ...resources on the Addgene blog CRISPR 101: Off-Target Effects Enhancing CRISPR Targeting Specificity with ...inventory of kit contents Brush up with our CRISPR Guide Read our CRISPR 101 eBook  ...By Balázs Csoma, Hungarian Research Network CRISPR nucleases are remarkably precise molecular tools for...does not mean “perfectly specific.” In reality, CRISPR nucleases occasionally make mistakes and cleave.... A practical sgRNA design note When expressing gRNAs from a U6 promoter, remember that transcription ...does not naturally begin with a purine, extend the gRNA with a 5′ G (21G design). Be aware that only certain...approach. This post was written by Balázs Csoma, a CRISPR biologist working on improved genome editing at...
  10. Using Addgene's New Viral Service for Your Research

    Type
    Blog Post
    Published
    Nov. 17, 2016, 3:30 p.m.
    ... Cas9 activators, Cas9 repressors, select gRNAs, and CRISPR pooled libraries. Whether you’d like to knockout...Service, we’re distributing lentivirus (with many CRISPR tools included among the preps that are currently...lentiviral vectors in the repository are used to produce CRISPR tools, we’re starting the Viral Service with lentiviral... in experiments other than just those involving CRISPR and so we also have lentivirus for delivering control...
  11. Plasmids 101: The protein expression toolbox

    Type
    Blog Post
    Published
    Feb. 16, 2023, 7:05 p.m.
    ... gene for your protein of interest. CRISPR-Cas9 and a custom gRNA is all you need to generate a frameshift...protein levels for 1-3 days. There’s also a CRISPR for that! CRISPR interference (CRISPRi) targets a catalytically...for just a little while Yes, there’s a CRISPR for that, too! CRISPR activators (CRISPRa) are transcriptional... to a dead Cas9. The system is led, via a custom gRNA, to your gene of interest to temporarily increase... about them on our CRISPRa blog! Fig. 1 CRISPR activator and repressor mechanisms Want to... Promoters Plasmid 101: Repressible Promoters CRISPR 101: Which Cas9 Do I Choose for my Experiment ...resources on the Addgene website Promoter Guide CRISPR Guide Lentiviral Guide  ...
  12. Targeted Mutagenesis with EvolvR

    Type
    Blog Post
    Published
    Feb. 21, 2019, 1:15 p.m.
    ...Resources on Addgene.org Browse our CRISPR guide pages Find bacterial CRISPR plasmids ...within a user-defined genomic region. EvolvR, a CRISPR-Cas9 based targeted mutagenesis method developed...for targeted mutagenesis of a site of interest. A gRNA is used to direct the PolI3M-nCas9 complex to a ...window also increased the likelihood that a single gRNA would introduce more than one mutation near the ... Pablo Perez-Pinera. "The continuously evolving CRISPR barcoding toolbox." Genome biology 19.1 (2018):...PMCID: PMC6154929. Halperin, Shakked O., et al. "CRISPR-guided DNA polymerases enable diversification of...resources on the Addgene blog Learn about other CRISPR methods for bacterial genome engineering   Learn...
  13. Hot Plasmids and Viral Preps - January 2021

    Type
    Blog Post
    Published
    Jan. 5, 2021, 2:15 p.m.
    ...for use in bacteria CRISPR-Casɸ mGold, a new yellow fluorescent protein New CRISPR plasmids New items ...Hypercompact genome editor CRISPR-Casɸ By Melina Fan The Doudna Lab adds to the CRISPR-Cas toolbox with their...sciadv.abb7438 The CRISPR corner By Jennifer Tsang Here are a few highlights from recent CRISPR plasmids. To...To find all of the CRISPR plasmids available from Addgene, head over to our CRISPR Plasmids and Resources...functionalized gRNAs.  Find the yeast CRISPRa plasmids here Reduce the scale of your CRISPR screens by ...their discovery of CRISPR-Casɸ, a hypercompact genome editor from the Biggiephage clade of huge phages. ... B is G, T, or C). The authors demonstrate that CRISPR-Casɸ is active in vitro as well as in human and...
  14. Four Ways to Package Transgenes That Exceed the Size Limit of Adeno-associated Virus

    Type
    Blog Post
    Published
    Sept. 1, 2020, 1:15 p.m.
    ...increasing the size of the AAV donor template for CRISPR-mediated homology directed repairs (HDR). Split...sequential homology directed repairs (HDR) with CRISPR/Cas9. Donor A contains: 400bp homology arms to ... for integration, “part A” of the transgene, the gRNA target site that mediated the donor template’s integration...integration; and a sequence of stuffer DNA after the gRNA target site. Donor B contains: 400 bp homology ...single step and serve as donors for two consecutive CRISPR-mediated HDR events which results in the integration...if non-homologous end joining (NHEJ) disrupts the gRNA target site after the first HDR event, then the ...A in any of the reading frames downstream of the gRNA target site so that transcripts undergo nonstop ...
  15. dTAG - You're it!

    Type
    Blog Post
    Published
    June 21, 2018, 2:06 p.m.
    ...Addgene.org Browse all CRISPR plasmids CRISPR plasmids for protein tagging Find validated gRNAs ...Addgene Blog Easi-CRISPR: Generating Knock-In and Conditional Mouse Models CRISPR 101: Cas9 Nickase Design... selective degradation of FKBP12F36V-BRD4 using CRISPR/Cas9-mediated knock-in, and to evaluate in vivo...ENL-FKBP12F36V and endogenous ENL was inactivated using CRISPR/Cas9 gene-editing. Featured molecules: dTAG-7 and...-MELK and endogenous MELK was inactivated using CRISPR/Cas9 gene-editing. Featured molecules: dTAG-7, ...were engineered to express YY1-FKBP12F36V using CRISPR/Cas9-mediated knock-in. Featured molecule: dTAG...
  16. Addgene’s Top 10 Blog Posts from 2014

    Type
    Blog Post
    Published
    Dec. 16, 2014, 8:01 p.m.
    ...and improved. The CRISPR posts written by our guest bloggers, the experts in the CRISPR/Cas field, have ...Popular Posts of 2014 How to Design Your gRNA for CRISPR Genome Editing By John Doench (Guest Blogger...past year. A quick glance shows that interest in CRISPR continues to grow as the genome editing technique...Plasmids 101: Yeast Vectors By Marcy Patrick CRISPR-Cas9 FAQs Answered! By Caroline LaManna Plasmids...
  17. Quickest Way to Deposit Plasmids: The Deposit Spreadsheet

    Type
    Blog Post
    Published
    March 8, 2017, 3:15 p.m.
    ...Addgene Plasmids Searchable and Sortable gRNAs for Your Next CRISPR Experiment Suggest A Plasmid You'd Like... Type Choose from: Encodes one insert, encodes gRNA/shRNA, or empty backbone. Purpose Answer “... expression, plant expression, mouse targeting, CRISPR, TALEN, synthetic biology, affinity reagent/antibody...
  18. Plasmids 101: NGS Quality Control for Pooled Libraries

    Type
    Blog Post
    Published
    Oct. 26, 2017, 1:59 p.m.
    ...re-amplified our distribution stock of the Brunello Human gRNA library, and we thought it would be a good time ... the plasmids are all very similar sizes, like a gRNA library, this is less of a concern, but Addgene ...confirmed using next-generation sequencing (NGS). For gRNA libraries, you’ll design primers to create 200-300...Sequencing to Validate AAV Preps Learn More about Pooled CRISPR Libraries Resources on Addgene.org Browse Pooled...
  19. A New Generation of Adenine Base Editors Improves Editing in Primary Human Cells

    Type
    Blog Post
    Published
    May 7, 2020, 1:15 p.m.
    ...xCas9, a CRISPR variant with PAM flexibility Resources on Addgene.org Get the basics of CRISPR in our ...our CRISPR guide Find all plasmids for base editing in our collection Sign up to get our free CRISPR eBook...cellular DNA and RNA dependent or independent of the gRNA used (Gaudelli et al., 2017). The authors tested...al., 2020) was able to reduce off-target RNA and gRNA-dependent DNA editing while maintaining on-target...
  20. Pushing the Limits of DNA Assembly

    Type
    Blog Post
    Published
    Sept. 6, 2017, 1:01 p.m.
    ...Resources on Addgene.org Browse Our CRISPR Resources Find Validated gRNAs Browse All Plasmids ...sgRNAs Generating constructs to produce sgRNA for CRISPR experiments can be laborious, requiring multiple...
Showing: 121 - 140 of 159 results