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Product List
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- Cat. No.: C305
- Price: $145.00
- Unit:1.0 µg DNA
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Description:
The Adeno-Associated Virus (AAV) offers a uniquely flexible delivery method for the revolutionary gene editing technology, CRISPR Cas9. These small, but powerful viruses open the door to virus-based gene therapy, thanks to a broad range of attractive properties, such as:
- Ability to infect both dividing and non-dividing cells
- Low immunogenicity and pathogenicity
- Ability to target a broad range of tissue types
- Long-term expression in non-dividing cells
Our custom design service harnesses the power of CRISPR Cas9 to enable gene editing in a wide range of cell types, both in culture, and animal models. We can supply custom-designed sgRNA-expressing AAV vectors for virtually any application. Our vectors can deliver sgRNAs efficiently into any cells already expressing the Cas9 nuclease, thus targeting the CRISPR Cas9 machinery to trigger gene editing at will.
But that’s not all! For an even simpler experimental setup, we also offer all-in-one CRISPR Cas9 vectors expressing both the compact saCas9 variant, and custom-designed sgRNAs. Simply provide us with a description of your gene editing experiment, and we will deliver viral vectors, as well as pre-packaged viruses, right to your fingertips!
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- Cat. No.: C306
- Price: $465.00
- Unit:3 x 1.0 µg DNA
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Description:
The Adeno-Associated Virus (AAV) offers a uniquely flexible delivery method for the revolutionary gene editing technology, CRISPR Cas9. These small, but powerful viruses open the door to virus-based gene therapy, thanks to a broad range of attractive properties, such as:
- Ability to infect both dividing and non-dividing cells
- Low immunogenicity and pathogenicity
- Ability to target a broad range of tissue types
- Long-term expression in non-dividing cells
Our custom design service harnesses the power of CRISPR Cas9 to enable gene editing in a wide range of cell types, both in culture, and animal models. We can supply custom-designed sgRNA-expressing AAV vectors for virtually any application. Our vectors can deliver sgRNAs efficiently into any cells already expressing the Cas9 nuclease, thus targeting the CRISPR Cas9 machinery to trigger gene editing at will.
But that’s not all! For an even simpler experimental setup, we also offer all-in-one CRISPR Cas9 vectors expressing both the compact saCas9 variant, and custom-designed sgRNAs. Simply provide us with a description of your gene editing experiment, and we will deliver viral vectors, as well as pre-packaged viruses, right to your fingertips!
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- Cat. No.: C307
- Price: Inquiry
- Unit:1.0 µg DNA
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Description:
The Adeno-Associated Virus (AAV) offers a uniquely flexible delivery method for the revolutionary gene editing technology, CRISPR Cas9. These small, but powerful viruses open the door to virus-based gene therapy, thanks to a broad range of attractive properties, such as:
- Ability to infect both dividing and non-dividing cells
- Low immunogenicity and pathogenicity
- Ability to target a broad range of tissue types
- Long-term expression in non-dividing cells
Our custom design service harnesses the power of CRISPR Cas9 to enable gene editing in a wide range of cell types, both in culture, and animal models. We can supply custom-designed sgRNA-expressing AAV vectors for virtually any application. Our vectors can deliver sgRNAs efficiently into any cells already expressing the Cas9 nuclease, thus targeting the CRISPR Cas9 machinery to trigger gene editing at will.
But that’s not all! For an even simpler experimental setup, we also offer all-in-one CRISPR Cas9 vectors expressing both the compact saCas9 variant, and custom-designed sgRNAs. Simply provide us with a description of your gene editing experiment, and we will deliver viral vectors, as well as pre-packaged viruses, right to your fingertips!
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- Cat. No.: C438
- Price: $105.00
- Unit:1.0 µg
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Description:
abm offers CRISPR sgRNA and All-In-One constructs in convenient lentivector and lentivirus formats. Lentivirus allows for integration of your CRISPR components for long term expression, and enables genome editing in difficult-to-transfect cells. Our custom-designed lentivectors and lentiviruses can efficiently deliver sgRNAs into any Cas9-expressing cells to trigger CRISPR gene editing of your gene of interest. Or use our CRISPR All-In-One lentivectors to express your custom-targeted sgRNA simultaneously with spCas9 in one convenient package.
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- Cat. No.: C439
- Price: $135.00
- Unit:1.0 µg
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Description:
Abm’s non-viral vector is a simple method to achieve efficient, on-target gene editing using the CRISPR Cas9 system. Use direct transfection of our sgRNA plasmids for immediate expression of sgRNAs targeting your gene of interest. Or, for further ease of use, our non-viral vectors are also offered as a CRISPR Knockout All-In-One construct, which expresses Cas9 in conjunction with sgRNA. CRISPR plasmids are ideal for expressing sgRNA in a transient manner, limiting its off-target effects.
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- Cat. No.: C440
- Price: $125.00
- Unit:1.0 µg
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Description:
Abm’s non-viral vector is a simple method to achieve efficient, on-target gene editing using the CRISPR Cas9 system. Use direct transfection of our sgRNA plasmids for immediate expression of sgRNAs targeting your gene of interest. Or, for further ease of use, our non-viral vectors are also offered as a CRISPR Knockout All-In-One construct, which expresses Cas9 in conjunction with sgRNA. CRISPR plasmids are ideal for expressing sgRNA in a transient manner, limiting its off-target effects.
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- Cat. No.: C437
- Price: $95.00
- Unit:1.0 µg
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Description:
abm offers CRISPR sgRNA and All-In-One constructs in convenient lentivector and lentivirus formats. Lentivirus allows for integration of your CRISPR components for long term expression, and enables genome editing in difficult-to-transfect cells. Our custom-designed lentivectors and lentiviruses can efficiently deliver sgRNAs into any Cas9-expressing cells to trigger CRISPR gene editing of your gene of interest. Or use our CRISPR All-In-One lentivectors to express your custom-targeted sgRNA simultaneously with spCas9 in one convenient package.
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- Cat. No.: C441
- Price: $250.00
- Unit:3 x 1.0 µg
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Description:
abm offers CRISPR sgRNA and All-In-One constructs in convenient lentivector and lentivirus formats. Lentivirus allows for integration of your CRISPR components for long term expression, and enables genome editing in difficult-to-transfect cells. Our custom-designed lentivectors and lentiviruses can efficiently deliver sgRNAs into any Cas9-expressing cells to trigger CRISPR gene editing of your gene of interest. Or use our CRISPR All-In-One lentivectors to express your custom-targeted sgRNA simultaneously with spCas9 in one convenient package.
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- Cat. No.: C442
- Price: $280.00
- Unit:3 x 1.0 µg
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Description:
abm offers CRISPR sgRNA and All-In-One constructs in convenient lentivector and lentivirus formats. Lentivirus allows for integration of your CRISPR components for long term expression, and enables genome editing in difficult-to-transfect cells. Our custom-designed lentivectors and lentiviruses can efficiently deliver sgRNAs into any Cas9-expressing cells to trigger CRISPR gene editing of your gene of interest. Or use our CRISPR All-In-One lentivectors to express your custom-targeted sgRNA simultaneously with spCas9 in one convenient package.
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- Cat. No.: C443
- Price: $355.00
- Unit:3 x 1.0 µg
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Description:
Abm’s non-viral vector is a simple method to achieve efficient, on-target gene editing using the CRISPR Cas9 system. Use direct transfection of our sgRNA plasmids for immediate expression of sgRNAs targeting your gene of interest. Or, for further ease of use, our non-viral vectors are also offered as a CRISPR Knockout All-In-One construct, which expresses Cas9 in conjunction with sgRNA. CRISPR plasmids are ideal for expressing sgRNA in a transient manner, limiting its off-target effects.