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Nancy Petitclerc, Immuni T, Immortalized Cell Lines
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Search our extensive cell line collection, Including Primary, Immortalized, Drug Discovery, Reporter, and Tumor cell lines.
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Cell Culture – An Introduction
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Top Publications
MicroRNA-9 inhibits hyperglycemia-induced pyroptosis in human ventricular cardiomyocytes by targeting ELAVL1.
Jeyabal, P., et al.
Biochem Biophys Res Commun.
doi: 10.1016/j.bbrc.2016.02.065.
NBR1 enables autophagy-dependent focal adhesion turnover.
Kenific, CM., et al.
J Cell Biol. (2016) 212(5): 577-90. (2016)
doi: 10.1083/jcb.201503075.
Characterizing primary human microglia: A comparative study with myeloid subsets and culture models.
Melief, J., et al.
Glia. (2016) 64(11): 1857-68.
doi:10.1002/glia.23023.
Testimonials
ABM has always been very helpful with technical assistance in any of our questions and concerns. I also consider the price for the services provided as very competitive, as other companies charge a multiple of ABM's price. I would highly recommend ABM's service to any customer interested in custom-made pluripotent stem cells.
Dr. Cameron Moshfegh
ETH Zurich
iPSC Generation
I really like to order from ABM as the ordering process is fairly straight forward and the documentation provided, especially with the cell lines, is very well detailed and complete.
Nancy Petitclerc
Immuni T
Immortalized Cell Lines
We are quite happy with the knockout cells that you made. This was a tricky knockout and hemizygous removal was much more prevalent than the double knockout, but you did it. In addition to your excellent genomic sequence characterization of both mutant LIF alleles, I have confirmed in our lab that the tumor cells have lost all mouse LIF production.
Dr. Robert Jackman
Boston University
Mouse LIF CRISPR Knock Out C26 Tumor Cell Line Generation and Screening Service
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Unit: 1x106 cells / 1.0 mlThrough lentiviral infection, the IRES-GFP Stable LUHMES Cell Line was generated.abm also offers A30P aSYN-IRES-GFP Stable LUHMES Cell Line (T6454), and A53T aSYN-IRES-GFP Stable LUHMES Cell Line (T6455), Wild Type aSYN-IRES-GFP Stable LUHMES Cell...
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Unit: 1x106 cells / 1.0 mlThrough lentiviral infection, the Wild Type aSYN-IRES-GFP Stable LUHMES Cell Line was generated. The cells stably express wild type aSyn. This cell line can be used to study neurotoxicity and to identify targets for treatment/prevention of...
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Unit: 1x106 cells / 1.0 mlThrough lentiviral infection, the A53T aSYN-IRES-GFP Stable LUHMES Cell Line was generated. The cells stably express A53T aSyn. This cell line can be used to study neurotoxicity and to identify targets for treatment/prevention of neurodegenerative...
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Unit: 1x106 cells / 1.0 mlThrough lentiviral infection, the A30P aSYN-IRES-GFP Stable LUHMES Cell Line was generated. The cells stably express A30P aSyn. This cell line can be used to study neurotoxicity and to identify targets for treatment/prevention of neurodegenerative...
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Unit: 1x106 cells / 1.0 mlH295RA is an ACTH-responsive human adrenocortical cell line, produced from H295R cells that have been transduced to stable express increased human MRAP (MC2R accessory protein) gene. H295R adrenocortical cell line displays relatively low ACTH...
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Unit: 1x106 cells / 1.0 mlLhx5 is a transcription factor with restricted Mamillary body (MBO) expression. LHX5 is a member of the LHX family of transcription factors acting as important differentiation determinants, and it is strongly expressed in the caudal hypothalamus...
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Unit: 1x106 cells / 1.0 mlFusing a kinase domain to a homodimerization domain such as the PNT domain of ETV6 can result in activated kinase. The KDR Stable Ba/F3 Cell Line expresses activated KDR tyrosine kinase that is linked to a GFP reporter (GFP-ETV6-KDR). KDR belongs to...
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Unit: 1x106 cells / 1.0 mlCells 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...
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Unit: 1x106 cells / 1.0 mlCells 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...