PrecisionXTM OnTargetTM Gene Knock-out HR Targeting Vector (MCS1-EF1α-Blasticidin-pA-MCS2-PGK-hsvTK)

Enrich for on-target integrants via negative TK selection with this knock-out and editing HR targeting vector—also features blasticidin selection

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Gene Knock-Out HR Targeting Vector w/Single Selection Marker (Blasticidin) and Negative Selection (TK) Against Random Integration

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Gene Knock-Out HR Targeting Vector w/Single Selection Marker (Blasticidin) and Negative Selection (TK) Against Random Integration

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10 µg
HR720PA-1
$ 963
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Overview

Select against off-target events with OnTargetTM HR Targeting Vectors

Use the PrecisionXTM OnTargetTM Gene Knock-out HR Targeting Vector (MCS1-EF1α-Blasticidin-pA-MCS2-PGK-hsvTK) to knock-out any gene or edit the genome. Clone your homology arms into MCS1 and MCS2, and use blasticidin selection to find integrants. Even better, with this series of OnTargetTM HR Donors, you can enrich for on-target events using negative thymidine kinase (TK) selection (Figure 1). After you’ve identified clones with your gene-of-interest knocked-out or edited, you can remove the selection cassette using the Cre-LoxP system (learn more about Cre-LoxP excision here).

PrecisionX Gene Knock-out HR Targeting Vector (MCS1-EF1α-Blasticidin-pA-MCS2-PGK-hsvTK)Using negative TK selection to enrich for on-target events

Figure 1. Using negative TK selection to enrich for on-target events. With on target HR Donor-mediated gene editing (left column), the homology arms of the HR Donor drive homologous recombination, resulting in insertion of only the region of the HR Donor that lies between the two homology arms—if the PGK-hsvTK cassette is outside of the homology arms, it will not be inserted into the genome and cells will not be sensitive to ganciclovir or fialuridine.
However, with off target insertion of the HR Donor (right column), integration is not mediated by homology, resulting in insertion of the entire HR Donor Vector. If the HR Donor includes the PGK-hsvTK cassette, even if the cassette is outside of the homology arms, the cassette will get inserted into the genome, rendering the cells sensitive to ganciclovir or fialuridine and enabling negative selection against off-target events.

Why use an HR targeting vector?

Even though gene knock-outs can result from DSBs caused by Cas9 alone, SBI recommends the use of HR targeting vectors (also called HR donor vectors) for more efficient and precise mutation. HR donors can supply elements for positive or negative selection ensuring easier identification of successful mutation events. In addition, HR donors can include up to 6-8 kb of open reading frame for gene knock-ins or tagging, and, when small mutations are included in either 5’ or 3’ homology arms, can make specific, targeted gene edits.

Choose the right HR Targeting Vector for your project

Catalog # HR Donor Vector Features* Application
Gene Knock-out Gene Knock-in Gene Edits Gene Tagging
HR100PA-1 MCS1-LoxP-MCS2-MCS3-pA-LoxP-MCS4 Basic HR Donor
HR110PA-1 MCS1-EF1α-RFP-T2A-Puro-pA-MCS2 Removable RFP marker and puromycin selection
HR120PA-1 GFP-pA-LoxP-EF1α-RFP-T2A-Puro-pA-LoxP-MCSPuro-pA-LoxP-MCS Tag with GFP fusion
Removable RFP marker and puromycin selection
HR130PA-1 T2A-GFP-pA-loxP-EF1α-RFP-T2A-Puro-pA-LoxP-MCSA-loxP-EF1α-RFP-T2A-Puro-pA-LoxP-MCS Co-express GFP with “tagged” gene via T2A
Removable RFP marker and puromycin selection
HR150PA-1 GFP-T2A-Luc-pA-loxP-EF1α-RFP-T2A-Puro-pA-LoxP-MCS Tag with GFP fusion and co-express luciferase via T2A
Removable RFP marker and puromycin selection
HR180PA-1 IRES-GFP-pA-loxP-MCS1-EF1α-RFP-T2A-Puro-pA-LoxP-MCS2 Co-express GFP with “tagged” gene via IRES
Removable RFP marker and puromycin selection
HR210PA-1 MCS1-LoxP-EF1α-GFP-T2A-Puro-P2A-hsvTK-pA-LoxP-MCS2 Removable GFP marker, puromycin selection, and TK selection
HR220PA-1 GFP-pA-LoxP-EF1α-RFP-T2A-Hygro-pA-LoxP-MCS Tag with GFP fusion
Removable RFP ,arker and hygromycin Selection
HR410PA-1 MCS1-EF1α-GFP-T2A-Puro-pA-MCS2 Removable GFP marker and puromycin selection
HR510PA-1 MCS1-EF1α-RFP-T2A-Hygro-pA-MCS2 Removable RFP marker and hygromycin selection
HR700PA-1 MCS1-EF1α-GFP-T2A-Puro-pA-MCS2-PGK-hsvTK Enrich for on-target integration with negative TK selection**
Removable GFP marker and puromycin selection
HR710PA-1 MCS1-EF1α-RFP-T2A-Hygro-pA-MCS2-PGK-hsvTK Enrich for on-target integration with negative TK selection**
Removable RFP marker and hygromycin selection
HR720PA-1 MCS1-EF1α-Blasticidin-pA-MCS2-PGK-hsvTK Enrich for on-target integration with negative TK selection**
Removable blasticidin selection
GE602A-1 pAAVS1D-PGK-MCS-EF1α-copGFPpuro First generation AAVS1-targeting HR Donor
GE603A-1 pAAVS1D-CMV-RFP-EF1α-copGFPpuro First generation AAVS1-targeting HR Donor (positive control for GE602A-1)
GE620A-1 AAVS1-SA-puro-MCS Second generation AAVS1-targeting HR Donor
Promoterless to knock-in any gene or promoter-gene combination
GE622A-1 AAVS1-SA-puro-EF1α-MCS Second generation AAVS1-targeting HR Donor
Constitutive expression of your gene-of-interest
GE624A-1 AAVS1-SA-puro-MCS-GFP Second generation AAVS1-targeting HR Donor
Create reporter cell lines
CAS620A-1 AAVS1-SA-puro-EF1α-hspCas9 Knock-in Cas9 to the AAVS1 site
PBHR100A-1 MCS1-5'PB TR-EF1α-GFP-T2A-Puro-T2A-hsvTK-pA-3' PB TR-MCS2 Use with the PiggyBac Transposon System
Enables seamless gene editing with no residual footprint (i.e. completely remove vector sequences)
*All HR Target Vectors except PBHR100A-1 contain LoxP sites. Any sequences that are integrated between the two LoxP sites can be removed through transient expression of Cre Recombinase.
**The clever design of these HR Donors enables enrichment for on-target integration events. A PGK-hsvTK cassette is included outside of the homology arms. Because of this configuration, on-target integration that results from homologous recombination will not include the PGK-hsvTK cassette—only randomly-integrated off-target events will lead to integration of PGK-hsvTK and resulting TK activity. Therefore, TK selection will negatively select against off-target integrants. Click on any one of these vectors to see a diagram of how the negative selection works.

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How It Works

At-a-glance—how to use an HR Targeting Vector to knock-out a gene

Using an HR Donor Vector and the CRISPR/Cas9 System to knock-out a gene

Figure 2. Knocking-out a gene using an HR Targeting Vector. Step 1: Cas9 creates a double-stranded break (DSB) in the genomic DNA at a site that is complimentary to the gRNA. Step 2: The DNA repair machinery is recruited to the DSB. In the presence of an HR Donor with homology to the region adjacent to the DSB (blue areas of the genomic and vector DNA) homologous recombination (HR) is favored over non-homologous end joining (NHEJ). Result: The HR event leads to insertion of the region of the HR Donor Vector between the two homology arms—your selection cassette is integrated into the gene, disrupting the open reading frame.

At-a-glance—how to use an HR Targeting Vector to edit a geneUsing an HR Donor Vector and the CRISPR/Cas9 System to edit a gene

Figure 3. Editing a gene using an HR Targeting Vector. Step 1: Cas9 creates a double-stranded break (DSB) in the genomic DNA at a site that is complimentary to the gRNA. For gene editing, this DSB should be within an intron. Step 2: The DNA repair machinery is recruited to the DSB. In the presence of an HR Donor with homology to the region adjacent to the DSB (blue areas of the genomic and vector DNA) homologous recombination (HR) is favored over non-homologous end joining (NHEJ). If one of the homology arms of the HR donor contains the gene edit, it will be incorporated into the gene through the HR repair process. Step 3: Transient expression of Cre recombinase will result in excision of the selection cassette, leaving behind a single intronic LoxP site.

Genome engineering with CRISPR/Cas9

For general guidance on using CRISPR/Cas9 technology for genome engineering, including the design of HR Targeting Vectors, take a look at our CRISPR/Cas9 tutorials as well as the following application notes:

CRISPR/Cas9 Gene Knock-Out Application Note (PDF) »
CRISPR/Cas9 Gene Editing Application Note (PDF) »
CRISPR/Cas9 Gene Tagging Application Note (PDF) »