Virus Production 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 the expression, purification, and packaging of viruses and particles. Such services can offer researchers the advantages of high-quality and high-titer vectors, ready-to-transfect particles, and a reasonable turnaround time. In deciding on a service, among the factors to consider include the desired virus or vector type, such as baculovirus, adenovirus, or lentivirus.
Your search returned 138 Virus Production Services across 12 suppliers.
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- Our AAV team will design your custom AAV constructs and will manufacture ready-for-use viral particles to transduce your gene(s) of interest. Applications include CRISPR-mediated genetic engineering, protein expression, and the design and ...
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- BPS Bioscience has developed a diverse portfolio of lentivirus products to study COVID-19, cell signaling pathways, CAR T-cell therapy, CRISPR, and immunotherapy. In addition to our product portfolio, we also offer custom services to develop a ...
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- ABEOMICS' facility in San Diego, CA is well-suited to provide custom and contract production of your biologic proteins, essential for the production of protein drugs and to the development of drug assays and life science research. Our protein ...
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- Addgene's viral service provides high-quality and high-titer viral preparations. Addgene's AAV are made from plasmids that are currently in our repository. You can obtain the plasmid from us or receive a ready-to-use viral preparation from our ...
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- Complete AAV services including: proprietary AAV ITR sequencing, AAV plasmid synthesis and ITR correction, AAV plasmid preparation, and AAV packaging with more than 20 serotype options. Work with GENEWIZ at any point in your AAV development workflow...
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- High-throughput synthesis, prep and packaging of lentiviral plasmids for high-titer viral production.
- Lentiviral expression vectors are one of the most effective vehicles to introduce and stably express different effector molecules or reporter constructs in almost any mammalian cell, including non dividing cells and whole model organisms. Our ...
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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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- Lentiviral expression vectors are one of the most effective vehicles to introduce and stably express different effector molecules or reporter constructs in almost any mammalian cell, including non dividing cells and whole model organisms. Our ...
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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 in almost any mammalian cell, including non dividing cells and whole model organisms. Our ...
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
- 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
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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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- Cellecta can provide any of its lentiviral constructs or libraries as ready-to-transduce, pre-packaged as VSV-g pseudotyped lentiviral particles. These lentiviral preparations can be directly added to cells in culture. The lentiviral particles fuse ...
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- Cellecta can provide any of its lentiviral constructs or libraries as ready-to-transduce, pre-packaged as VSV-g pseudotyped lentiviral particles. These lentiviral preparations can be directly added to cells in culture. The lentiviral particles fuse ...
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- Cellecta can provide any of its lentiviral constructs or libraries as ready-to-transduce, pre-packaged as VSV-g pseudotyped lentiviral particles. These lentiviral preparations can be directly added to cells in culture. The lentiviral particles fuse ...
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- Cellecta can provide any of its lentiviral constructs or libraries as ready-to-transduce, pre-packaged as VSV-g pseudotyped lentiviral particles. These lentiviral preparations can be directly added to cells in culture. The lentiviral particles fuse ...
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- Cellecta can provide any of its lentiviral constructs or libraries as ready-to-transduce, pre-packaged as VSV-g pseudotyped lentiviral particles. These lentiviral preparations can be directly added to cells in culture. The lentiviral particles fuse ...
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- Cellecta can provide any of its lentiviral constructs or libraries as ready-to-transduce, pre-packaged as VSV-g pseudotyped lentiviral particles. These lentiviral preparations can be directly added to cells in culture. The lentiviral particles fuse ...
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- Cellecta can provide any of its lentiviral constructs or libraries as ready-to-transduce, pre-packaged as VSV-g pseudotyped lentiviral particles. These lentiviral preparations can be directly added to cells in culture. The lentiviral particles fuse ...
Read More
- Lentiviral expression vectors are one of the most effective vehicles to introduce and stably express different effector molecules or reporter constructs in almost any mammalian cell, including non dividing cells and whole model organisms. Our ...
Read More
- Cellecta can provide any of its lentiviral constructs or libraries as ready-to-transduce, pre-packaged as VSV-g pseudotyped lentiviral particles. These lentiviral preparations can be directly added to cells in culture. The lentiviral particles fuse ...
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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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- 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
- 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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