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 76 Virus Production Services across 9 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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- Sino Biological currently offers recombinant protein production services in baculovirus cell expression system. With the help of our optimized insect expression system, our team has rich experience in tailoring various challenging protein targets, ...
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- Creative Biolabs has abundant experience in the baculovirus-insect expression system.
- 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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- Quick Turnaround AAV Packaging for Research and Development
AAV, or adeno-associated virus, is a frequently used viral vector in many areas of research and development including cell and gene therapy, precision medicine, and vaccine development. Our...
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- Quick Turnaround Adenovirus Packaging for Research and Development
Adenovirus stands out as a powerful and versatile viral vector, driving innovation across cell and gene therapy, immunology, and oncology. At BioInnovatise, we specialize in ...
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- Lentivirus Packaging Service
Lentivirus is a versatile and highly utilized viral vector used in many areas of research and development including cell and gene therapy, immunology, and oncology. Our team is able to package your plasmid DNA construct ...
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- Retrovirus Packaging Service
Retrovirus is a versatile and effective viral vector used in many areas of research and development including cell and gene therapy, immunology, and oncology. Our team is able to package your plasmid DNA construct into ...
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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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- 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 ...
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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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- 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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