Cookie Consent by Free Privacy Policy Generator
Phone

+381 11 32 92 888

Email Adress

info@alfamed.rs

Recombinant Virus Packaging

Alfamed > Service > Recombinant Virus Packaging

Recombinant Virus Packaging

Power your gene delivery experiments with abm’s Recombinant Virus Packaging services—trusted by researchers for high-titre, ready-to-use viral vectors. Whether you're studying gene function, performing stable transductions, or delivering CRISPR components, abm provides reliable, scalable solutions tailored to your application.

abm's expertise spans a wide range of viral systems to meet diverse research needs. Choose from Recombinant Lentivirus for efficient gene delivery in dividing and non-dividing cells, Recombinant AAV for safe and long-term expression, Recombinant Adenovirus for high expression in a broad range of cells, or Recombinant Retrovirus for stable integration in dividing cells. Whatever your project, abm is here to help you achieve efficient and effective gene delivery, every time.

Custom Recombinant Lentivirus

As a leading expert in lentiviral technology, abm provides a Custom Lentivirus Service to support the design, cloning, and viral packaging of your unique lentivirus construct. We offer a range of research-grade lentivirus with ultra-high titers up to 10¹⁰ IU/ml to meet your experimental requirements. Need something different? Explore our ready-to-use gene libraries or inquire with us below to get started on your Custom Lentivirus project. 

Advantages of the Lentivirus System:

  • High infection efficiency
  • Stable integration & expression of recombinant proteins
  • Large insert capacity (up to 5kb)
  • Ideal system for the creation of stable cell lines
  • Broad host range: infection of dividing, non-dividing, stem cells, and primary cells
Documents

Custom Recombinant AAV

As a leading expert in AAV technology, abm provides a Custom AAV Service to assist with the design, cloning, and viral packaging of your unique AAV construct. abm offers a wide selection of AAV serotypes, including 1-11, AAV2/8, AAV2/9n, AAV2.7m8, PHP.eB, PHP.S, shH10 and Anc80L65. abm's purification options include crude preparations (ideal for in vitro experiments) and purified versions (optimized for in vivo applications). Inquire with abm to get started on your Custom AAV project. 

Advantages of the AAV System:

  • Used as a promising candidate for gene therapy
  • Does not elicit significant immune responses in vivo
  • Broad tropism - tissue specificity with different AAV serotypes
  • No integration into the host genome
  • Ability to transduce both proliferating and quiescent cells
  • Long-term expression in non-dividing cells
Documents

Custom Recombinant Adenovirus

abm offers a Custom Adenovirus Service where abm can gene synthesize, clone and viral package your custom adenovirus construct for you. abm offers a standard titer of 106 pfu/ml in addition to titer upgrades of 1010 pfu/ml and 1012 pfu/ml. Inquire with abm about your custom project and abm will take care of the rest!  

Advantages of the Adenovirus System:

  • High transduction efficiency in most mammalian cells
  • Low immunogenicity for high post-infection cell viability
  • Non-integrating and no risk of disrupting host genes
  • Broad host range (dividing, non-dividing, stem cells, and primary cells)
  • High titers can be obtained
  • Large insert capacity (up to 6 kb)
  • A popular choice in vivo and in vitro applications
  • Biosafety: abm use replication-incompetent (-E1/-E3) human adenovirus type 5 (Ad5).
Documents

Custom Recombinant Retrovirus

abm’s custom retroviruses are a highly-efficient method to achieve stable gene expression in a broad range of dividing mammalian cells. Simply send us your gene, or purchase an ORF vector from our extensive library of human, mouse, or rat genes, and abm will do the rest!

Documents