Gene Editing service options are available from several specialized providers. Choosing to outsource this application may not only save time and effort, but can also provide benefits from technical expertise and facilities dedicated to customized gene and genome editing. Such services can offer researchers the advantages of CRISPR-Cas9-based editing methods and comprehensive workflows--from experimental design, to cell line development and validation. In deciding on a service, among the factors to consider include the desired method of gene editing, such as CRISPR or TALEN.
Your search returned 49 Gene Editing Services across 8 suppliers.
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- CRISPR-Cas9 Services: Knock-In and Knock-Out Service
Quick Turnaround CRISPR-Cas9 Knock-Out and Knock-In Services for Research and Development
Unlock precise genome editing with our comprehensive CRISPR-Cas9 services. Our CRISPR knock-in and knock-...
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- Our cloning team specializes in creating, modifying, amplifying, and designing plasmid DNA that aligns to specific research objectives. To produce the research grade plasmid DNA researchers need, our team has assembled a comprehensive collection of ...
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- Our team offers Polymerase Chain Reaction (PCR) mutagenesis services on plasmid DNA constructs, both linear and circular, up to 18 kilobase pairs. Using primers to meet your mutation requirements, our team can match your mutation requirements on any ...
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- Our team offers Polymerase Chain Reaction (PCR) mutagenesis services on plasmid DNA constructs, both linear and circular, up to 18 kilobase pairs. Using primers to meet your mutation requirements, our team can match your mutation requirements on any ...
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- Our team offers Polymerase Chain Reaction (PCR) mutagenesis services on plasmid DNA constructs, both linear and circular, up to 18 kilobase pairs. Using primers to meet your mutation requirements, our team can match your mutation requirements on any ...
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- Our team offers Polymerase Chain Reaction (PCR) mutagenesis services on plasmid DNA constructs, both linear and circular, up to 18 kilobase pairs. Using primers to meet your mutation requirements, our team can match your mutation requirements on any ...
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- By taking advantage of array-based oligonucleotide synthesis, we can readily make precisely defined large custom pooled libraries expressing many thousands of elements. Within approximately 3 months, we can produce a completely new, high quality ...
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- By taking advantage of array-based oligonucleotide synthesis, we can readily make precisely defined large custom pooled libraries expressing many thousands of elements. Within approximately 3 months, we can produce a completely new, high quality ...
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- By taking advantage of array-based oligonucleotide synthesis, we can readily make precisely defined large custom pooled libraries expressing many thousands of elements. Within approximately 3 months, we can produce a completely new, high quality ...
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- The basis of Cellecta’s loss-of-function genetic screening technology is the stable suppression or knockout of specific genes on a large-scale using pooled shRNA or sgRNA libraries in mammalian cell systems. Genetic screens with shRNA or sgRNA ...
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- The basis of Cellecta’s loss-of-function genetic screening technology is the stable suppression or knockout of specific genes on a large-scale using pooled shRNA or sgRNA libraries in mammalian cell systems. Genetic screens with shRNA or sgRNA ...
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- The CRISPR/Cas9 system can be used for knocking out gene expression in vivo or in vitro by using a combination of an sgRNA (single guide RNA, or gRNA) along with a Cas9 nuclease. Achieve permanent 100% knockout in your cell line by using Cellecta&#...
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- Choose constitutive or inducible version of H1 or U6 shRNA promoters --Select GFP, RFP, PuroR, BleoR, NeoR, or Hygro-HK markers --Obtain constructs as plasmid or packaged lentiviral particles
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- The CRISPR/Cas9 system can be used for knocking out gene expression in vivo or in vitro by using a combination of an sgRNA (single guide RNA, or gRNA) along with a Cas9 nuclease. Achieve permanent 100% knockout in your cell line by using Cellecta&#...
Read More
- The CRISPR/Cas9 system can be used for knocking out gene expression in vivo or in vitro by using a combination of an sgRNA (single guide RNA, or gRNA) along with a Cas9 nuclease. Achieve permanent 100% knockout in your cell line by using Cellecta&#...
Read More
- Choose constitutive or inducible version of H1 or U6 shRNA promoters --Select GFP, RFP, PuroR, BleoR, NeoR, or Hygro-HK markers --Obtain constructs as plasmid or packaged lentiviral particles
Read More
- By taking advantage of array-based oligonucleotide synthesis, we can readily make precisely defined large custom pooled libraries expressing many thousands of elements. Within approximately 3 months, we can produce a completely new, high quality ...
Read More
- By taking advantage of array-based oligonucleotide synthesis, we can readily make precisely defined large custom pooled libraries expressing many thousands of elements. Within approximately 3 months, we can produce a completely new, high quality ...
Read More
- By taking advantage of array-based oligonucleotide synthesis, we can readily make precisely defined large custom pooled libraries expressing many thousands of elements. Within approximately 3 months, we can produce a completely new, high quality ...
Read More
- Cellecta can use the CRISPR/Cas9 system for screening. Start by using either the pooled CRISPR Human Genome Knockout Library or a Custom Pooled sgRNA Library targeting your own set of genes. After transducing cells with Cas9 and selecting cells ...
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- Cellecta can use the CRISPR/Cas9 system for screening. Start by using either the pooled CRISPR Human Genome Knockout Library or a Custom Pooled sgRNA Library targeting your own set of genes. After transducing cells with Cas9 and selecting cells ...
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- Cellecta offers custom isogenic knockout (CRISPR) services as part of its extensive functional genomics portfolio. Lentiviral technology enables efficient generation of stable isogenic cell lines starting from almost any mammalian cell. Cellecta&#...
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- Cellecta offers custom isogenic knockout (CRISPR) services as part of its extensive functional genomics portfolio. Lentiviral technology enables efficient generation of stable isogenic cell lines starting from almost any mammalian cell. Cellecta&#...
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- Cellecta offers custom isogenic knockout (CRISPR) services as part of its extensive functional genomics portfolio. Lentiviral technology enables efficient generation of stable isogenic cell lines starting from almost any mammalian cell. Cellecta&#...
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- CRISPR knockout requires expression of both a single-guide RNA (sgRNA) that targets the specific site for knockout, and expression of the Cas9 nuclease which cuts the DNA at the target site. While these two components can often be expressed from the ...
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- We can provide custom lentiviral constructs expressing any cDNA of interest as long as it is less than about 3.5 kb. Once we have the data, we: --synthesize the cDNA --clone the cDNA into the desired vector --sequence it to ensure proper construction
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- We can provide custom lentiviral constructs expressing any cDNA of interest as long as it is less than about 3.5 kb. Once we have the data, we: --synthesize the cDNA --clone the cDNA into the desired vector --sequence it to ensure proper construction
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- Transcription factor-dependent reporter cell lines can be ideal tools for high-throughput RNAi, peptide, and chemical library screens. With lentiviral-based transduction, Cellecta can easily engineer stable reporter lines for almost any application&#...
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- Transcription factor-dependent reporter cell lines can be ideal tools for high-throughput RNAi, peptide, and chemical library screens. With lentiviral-based transduction, Cellecta can easily engineer stable reporter lines for almost any application&#...
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- Lentiviral expression vectors are one of the most effective vehicles to introduce and stably express different effector molecules or reporter constructs into almost any mammalian cell, including non-dividing cells and whole model organisms. Let ...
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