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Expression of AcGFP1-tagged tubulin in iPS cells Efficient gene knockins in iPS cells using ssDNA
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Expression of AcGFP1-tagged tubulin in iPS cells Efficient gene knockins in iPS cells using ssDNA
Blog post about Marson paper Blog post: CRISPR takes a giant step towards the clinic

Guide-it Long ssDNA Production System v2

Long ssDNA for gene knockin experiments

The Guide-it Long ssDNA Production System v2 enables on-demand production of long single-stranded DNA (ssDNA) up to 5,000 nt in length for use as a repair template in knockin experiments involving CRISPR/Cas9 technology or other genome editing tools. This kit provides a simple and fast method for converting a dsDNA PCR product of any sequence into ssDNA via selective digestion of either the sense or the antisense strand. Each kit allows for preparation of 50 ssDNA templates.

The Guide-it Long ssDNA Production System v2 enables on-demand production of long single-stranded DNA (ssDNA) up to 5,000 nt in length for use as a repair template in knockin experiments involving CRISPR/Cas9 technology or other genome editing tools. This kit provides a simple and fast method for converting a dsDNA PCR product of any sequence into ssDNA via selective digestion of either the sense or the antisense strand. Each kit allows for the preparation of 50 ssDNA templates.

Although ssDNA templates have been shown to provide several important advantages over dsDNA templates for precise genome editing applications utilizing homology directed repair (HDR) (Roth et al., 2018), the use of long ssDNA has been limited due to the difficulty and cost of producing it. The Guide-it Long ssDNA Production System v2 is designed to make the benefits of ssDNA templates accessible to all researchers by providing an efficient, economical method for obtaining ssDNA on demand.

Benefits of using ssDNA as a template over dsDNA:

  • Significantly reduced random and off-target integration, resulting in improved gene editing efficiency and lower likelihood of experimental artefacts
  • Minimal cytotoxicity, enabling recovery of larger populations of edited cells
  • Negligible transgene expression from nonintegrated templates, allowing for easier identification of correctly edited clones
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Cat. # Product Size Price License Quantity Details
632666 Guide-it™ Long ssDNA Production System v2 50 Rxns USD $605.00

License Statement

ID Number  
M54 This product is covered by the claims of U.S. Patent Nos. 7,704,713 and its foreign counterparts. 

The Guide-it Long ssDNA Production System v2 includes all the reagents and materials necessary for on-demand preparation of single-stranded DNA (ssDNA) repair templates of any sequence up to 5,000 nt in length for engineering gene knockins using CRISPR/Cas9 technology or other genome editing tools. It has been demonstrated that ssDNA offers two key advantages over dsDNA templates for precise genome editing applications: greatly reduced toxicity and a much lower likelihood of random or off-target integration. The kit employs a simple and fast method that involves conversion of a dsDNA PCR product into ssDNA via selective digestion of either the sense or the antisense strand. Following digestion, ssDNA products are purified using silica membrane spin columns included with the kit.

Cat. # 632666 includes sufficient quantities of reagents and materials for preparation of 50 ssDNA templates.

Notice to purchaser

Our products are to be used for Research Use Only. They may not be used for any other purpose, including, but not limited to, use in humans, therapeutic or diagnostic use, or commercial use of any kind. Our products may not be transferred to third parties, resold, modified for resale, or used to manufacture commercial products or to provide a service to third parties without our prior written approval.

Documents Components Image Data

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Improved processing of challenging templates and production of ssDNA up to 5,000 nt with the Guide-it Long ssDNA Production System v2.

Improved processing of challenging templates and production of ssDNA up to 5,000 nt with the Guide-it Long ssDNA Production System v2.

Improved processing of challenging templates and production of ssDNA up to 5,000 nt with the Guide-it Long ssDNA Production System v2. The Guide-it Long ssDNA Production System v2 enables successful production of ssDNA ranging from 500 nt to 5,000 nt in length. The gel images show dsDNA substrates of varying length (Lane 1) and corresponding sense (SS) and antisense (AS) ssDNA products (Lane 2) following enzymatic digestion and cleanup with the kit. Each ssDNA HDR template was designed to target the CCR5 gene.

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Efficient editing and with negligible off-target insertion using ssDNA donor templates.

Efficient editing and with negligible off-target insertion using ssDNA donor templates.

Efficient editing and with negligible off-target insertion using ssDNA donor templates. Panel A. Tagging of GAPDH with a fluorescent protein (AcGFP1). An HDR template was designed to fuse the AcGFP1 coding sequence in-frame at the C-terminus of the GAPDH gene. Panel B. HEK293 cells were transfected with plasmid, dsDNA, or ssDNA forms of the AcGFP1 HDR template, with or without co-transfection of plasmids encoding for Cas9 and an sgRNA targeting the GAPDH locus. Cells were grown for three days and then analyzed by flow cytometry. While the plasmid template resulted in very little integration as demonstrated by the low percentages of fluorescent cells, the dsDNA yielded significant proportions of AcGFP1-postive cells, even in the absence of Cas9-sgRNA expression, suggesting a significant level of non-specific integration. Both sense (S) and antisense (A) ssDNA repair templates were associated with efficient insertion of the AcGFP1 sequence in the presence but not in the absence of Cas9 and sgRNA, suggesting that insertion of the AcGFP1 sequence was highly specific.

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Knockin of murine T-cell receptor α- and β-chains at the TRAC locus in human CD3+ T cells.

Knockin of murine T-cell receptor α- and β-chains at the TRAC locus in human CD3+ T cells.

Knockin of murine T-cell receptor α- and β-chains at the TRAC locus in human CD3+ T cells. Panel A. CRISPR/Cas9 RNPs with sgRNAs targeting both TRAC and TRBC loci were coelectroporated with an ssDNA HDR template encoding murine T-cell receptor α- and β-chains. The HDR template was designed to include 350-nt homology arms targeting exon 1 of the TRAC locus in addition to the following elements: P2A and T2A, self-cleaving peptide inserts; TRBC mouse, mouse TCR-β constant region; TRAC mouse, mouse TCR-α constant region; pGHpA, poly-A tail. The total length of the ssDNA was 2,800 nt. Panel B. Flow cytometric analysis of resulting T-cell populations 10 days after editing using antibodies against mouse TCR-β and human TCR-α/β. Cells in the negative control population (nonedited cells) were positive for the expression of human TCRs. For cells electroporated with RNPs targeting both TRAC and TRBC loci, knockout of the endogenous TCR could be detected. In cells coelectroporated with RNPs combined with the ssDNA HDR template, expression of the murine T-cell receptor α- and β-chains could be detected.

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632666: Guide-it Long ssDNA Production System v2

632666: Guide-it Long ssDNA Production System v2

HDR FAQs Homology-directed repair FAQs
Product finder tool for gene editing Gene editing product finder
Gene editing tools Gene editing tools and information

Overview

  • On-demand production of ssDNA donor templates ranging from 500–5,000 nt for gene knockin applications
  • Simple and fast protocol takes only a few hours to complete
  • Dramatically reduced off-target integration as compared to dsDNA templates
  • Minimal cytotoxicity, resulting in greater viability of edited cell populations

More Information

The Guide-it Long ssDNA Production System v2 includes refinements that enable more efficient processing of challenging templates, provide higher ssDNA yields, and allow for a simpler protocol as compared to our first-generation ssDNA kits (Cat. # 632644, 632645).*

Improved generation of ssDNA with the Guide-it Long ssDNA Production System v2. Gel image showing the dsDNA starting material (Lane 1) and sense (SS) or antisense (AS) ssDNA products for several HDR templates generated using the original (v1) or updated (v2) versions of the Guide-it Long ssDNA Production System (Lane 2 and Lane 3, respectively). dsDNA templates included in this analysis had been identified as challenging substrates for ssDNA generation using the v1 Guide-it kit. The dsDNA and ssDNA were analyzed via agarose gel electrophoresis using ethidium bromide as a staining agent. ssDNA products run at a smaller molecular weight than corresponding dsDNA substrates. In all cases, the Guide-it Long ssDNA Production System v2 generated a cleaner band of ssDNA than the previous version of the kit, suggesting more complete and uniform digestion.

*Please note that with the launch of the Guide-it Long ssDNA Production System v2, the original Guide-it ssDNA kits (Cat. # 632644, 632645) have been discontinued.

Additional product information

Please see the product's Certificate of Analysis for information about storage conditions, product components, and technical specifications. Please see the Kit Components List to determine kit components. Certificates of Analysis and Kit Components Lists are located under the Documents tab.


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Choose an HDR template format

Watch a webinar on how to choose the right HDR template for knockin experiments.

Homology-directed repair FAQs

Maximize your likelihood for success by reading these FAQs compiled by our R&D team.

Gene editing of T cells and HSCs

Follow these protocols developed by our R&D team for easy CRISPR/Cas-based gene editing of immune cells.

Site-specific gene knockins using long ssDNA

Gene knockins with long ssDNA sequences produced using Guide-it Long ssDNA Production System v2.

CRISPR/Cas9-mediated knockins in iPS cells

Data demonstrating efficient genome editing of iPS cells using HDR templates generated with the Guide-it Long ssDNA Production System.

CRISPR takes a giant step towards the clinic

Learn about the development of a powerful new method for reprogramming T cells.

Mouse CRISPR knockin protocol

Access a customer-developed protocol for precise genome editing in mouse embryos.

Electroporation-grade Cas9 for editing in diverse cell types

Our Cas9 performs highly efficient gene editing, including in iPS and hematopoietic stem cells.

Screening for effective guide RNAs

Before delivering sgRNA to your cells, use a novel in vitro assay to get accurate predictions of sgRNA cleavage efficiency.

Tag an endogenous gene with AcGFP1 in iPS cells

Workflow for tagging endogenous genes to generate reporter lines.

Tag an endogenous gene with a myc tag in iPS cells

Workflow for tagging endogenous genes with an epitope tag.

Efficient SNP engineering

Learn about a simple assay for sensitive detection of single-nucleotide substitutions in bulk-edited or clonal cell populations.

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