Drug Discovery Cell Lines

Leveraging abm’s proven success in the generation and validation of stable cell lines to accelerate your novel drug discoveries and biomedical research. Fully-validated, we have generated an unique library collection of G protein-coupled receptor (GPCR), Kinase, nuclear hormone receptor (NHR) and ion channel stable cell lines to provide powerful assay platforms for all research projects.

As a leader in gene expression and recombinant viral technology, we have streamlined the workflow from DNA construct cloning to recombinant viral vector generation and packaging, to gene expression quality control and to stable cell line generation for every gene in the human, mouse and rat genome. With our custom-tailored Whole-Genome Stable Cell Line solutions, the most difficult challenges in stable cell line creation can be overcome — so you can focus on answering the bigger questions in your project.

Search Drug Discovery Cell Lines Collection

Drug Discovery Cell Lines Collection

We offer wide selection of human, mouse, rat, and hamster drug discovery cell lines across more than 10 different cell systems.



Product Information

  • Characterization of BRITER cell line
    Characterization of BRITER cell line
    Characterization of the BRITER Cell Line (T3105), which has a BMP Response Element-dependent Firefly Luciferase gene.
  • cell culture workflow
    Cell Culture Workflow
    The SUNE2 cell line is derived from a nasopharyngeal carcinoma (NPC) from the biopsy performed on a 38-year-old female Cantonese patient.
  • Custom Stable Cell Line Generation Workflow
    Custom Stable Cell Line Generation Service
    abm provides a high quality and a cost-effective service for creating a cell line expressing your gene of interest with a fast turnaround time.

Top Publications

01 Inhibition of Lipid Oxidation Increases Glucose Metabolism and Enhances 2-Deoxy-2-[18F]Fluoro-d-Glucose Uptake in Prostate Cancer Mouse Xenografts.

Schlaepfer, I. R et al
Molecular Imaging and Biology 4:529-538 (2015).


DOI: 10.1007/s11307-014-0814-4.
02 Characterization of ryanodine receptor type 1 single channel activity using "on-nucleus" patch clamp.

Wagner, LE et al
Cell Calcium 56(2):96-107 (2014)


DOI: 10.1016/j.ceca.2014.05.004.

FAQs

Why do these cells need bio safety level II?
In order to be more cautious, we follow the CDC-NIH recommendations that all mammalian sourced products should be handled at the Biological Safety Level 2 to minimize exposure of potentially infectious products. This information can be found in 'Biosafety in Microbiological and Biomedical Laboratories' (1999). Your institution's Safety Officer or Technical Services will be able to make the call as to whether BioSafety Level I is possible with these cells at your site if required.
How do you test for the presence of replication incompetent lentivirus in these cell line products?
We perform this QC by testing viral titer of the culture media from each b atch using abm's qPCR titer kit (Cat# LV900), the results for which can be provided on the CoA for each lot#, upon request.
How long can I store frozen vials for?
Cells that are properly frozen using an effective cryoprotective agent can be stored in liquid nitrogen indefinitely without affecting their recovery.

Browse Products

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  1. Inquire
    Unit: 1x106 cells / 1.0 ml
    Cells were derived from HuH-7 cells. Cells were genetically modified using CRISPR/Cas9 method with 1 guide RNA and HDR template to heteroygously point mutate CYP3A5 *3 splice junction. Cells have very high CYP3A5 activity whereas the HuH-7 parental...


  2. Inquire
    Unit: 1x106 cells / 1.0 ml
    Cells were derived from HuH-7 cells. Cells were then genetically modified using CRISPR/Cas9 method with two guide RNAs to heterozygously delete CYP3A5 *3 splice junction. Cells have very high CYP3A5 activity whereas the HuH-7 parental cell line had...


  3. Inquire
    Unit: 1x106 cells / 1.0 ml
    Cells were derived from HuH-7 cells. Cells were then genetically modified using CRISPR/Cas9 method with two guide RNAs to homozygously delete CYP3A5 *3 splice junction. Cells have very high CYP3A5 activity whereas the HuH-7 parental cell line had...


  4. Inquire
    Unit: 1x106 cells/1.0ml
    293 cells stably expressing Human ACE2 


  5. Inquire
    Unit: 1x106 cells/1.0ml
    SF9 expressing SARS-CoV-2 Spike Glycoprotein S2 


  6. Inquire
    Unit: 1x106 cells/1.0ml
    CF9 cells expressing SARS-CoV-2 Spike Glycoprotein S1 


  7. Inquire
    Unit: 1x106 cells/1.0ml
    CHO-K1 cells were stably infected with Human ACE2. ACE2 is a SARS-CoV receptor located on the outer surface of cells.


  8. Inquire
    Unit: 1x106 cells/1.0ml
    The MDCK cell line has been used for many years for the production of virus vaccines. This STAT1 knockout MDCK cell line uses the CRISPR-Cas9 gene editing technology and it is useful for enhancing virus production capability when compared to...


  9. Inquire
    Unit: 1x106 cells/1.0ml
    The Vero cell line has been used for over 30 years for the production of virus vaccines. This STAT1 knockout Vero cell line uses the CRISPR-Cas9 gene editing technology and it is useful for enhancing virus production capability when compared to...


  10. Inquire
    Unit: 1x106 cells / 1.0 ml
    HEK293T cells stably expressing SARS-CoV Spike Glycoprotein. Useful for COVID-19 studies. 

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