TempoO2™
Oxygen Metabolism Biosensor Assay
TempoO2™
Oxygen Metabolism Biosensor Assay
TempoO2™, a fluorescent biosensor, is incorporated into Tempo’s proprietary immortalized human neuro-epithelial cell line, TempoRapid™. The biosensor assay offers fast kinetics (resolution: seconds to hours) in measuring real-time cellular metabolism and cytotoxicity. Analysis of cellular respiration directly reflects mitochondrial health and function. TempoO2™-Rapid cells serve as a control for all products containing the TempoO2™ biosensor. To customize TempoRapid™ cells to scientists’ experimental needs, the cells are easily transfectable with gene(s)-of-interest.
For filter-based instruments, Excitation/Emission: 617nm/635nm.
For monochromator-based instruments, Excitation 590nm +/- 20nm; Emission 650nm +/- 20nm.
Applications
TempoO2™ cells are intended for basic scientific research, drug discovery and therapeutics development use only. It is not a product for human testing or diagnostics.
Cytotoxicity Assays
Cellular Metabolism Assays
Chemical compound or small molecules testing
Live cell imaging (time-course studies and drug treatments).
For low, medium, or high-throughput applications
Easily transfected cells to test gene-of-interest function(s).
Specifications
~0.6×10^6 cells per 1ml of freezing medium (vial)
Long-term Storage: liquid nitrogen
Growth Properties: adherent
Storage: remove cryovials (dry ice packaging) and place the vial into liquid nitrogen for storage. Alternatively, thaw and use the cells immediately.
QC: Sterility, Safety (BioSafety Level 2), HIV/viruses, bacteria, fungi: negative. Cell viability post-thawing (>90%)
Product Use: TempoO2™-Rapid cells are intended for basic scientific research, drug discovery and therapeutics development use only. It is not a product for human testing or diagnostics.
TempoO2™-Rapid SKU402
Frequently Requested Cell Lines
The following are disease cell models that we are able to create through TempoO2
Cell Line Name | Histology Type | |
U2OS | Bone carcinoma | |
HEK293 | Immortalized Kidney Epithelial | |
SW 480 | Colorectal adenocarcinoma | |
U87MG | Brain cancer | |
Hep G2 | Hepatocellular carcinoma | |
NIH3T3 | Embroyonic fibroblast, murine | |
HT1080 | Carcinoma (connective tissue) | |
HCT116 | Colorectal cancer | |
MCF 7 | Breast cancer | |
SW 1990 | Pancreatic cancer | |
NCI-H2126 | Non-Small cell cancer | |
HUVEC | Umbilical vascular endothelium | |
HeLa | Cervical epithelial adenocarcinoma | |
CG4 | Glial cell line (from rat) | |
A-204 | Muscle epithelial | |
A549 | Lung epithelial cell line | |
BT-142 | Oligoastrocytoma, suspension | |
NK-92 | Peripheral blood, natural killer cells | |
CHO | Chinese hamster ovarian cell line | |
NCI-H69 | Lung tumor cell aggregate, suspension | |
ARPE-19 | Retinal pigmented epithelial | |
Beta-TC-6 | Beta cell (mouse) | |
BxPC-3 | Pancreatic epithelial, adenocarcinoma | |
Jurkat cells | Peripheral T lymphocyte, suspension | |
SW 780 | Urinary bladder epithelial carcinoma | |
MeT-5A | Mesothelium, from non-cancerous | |
NFKB reporters | Email us | |
Mesenchymal stromal cells | Email us | |
Chemokine Reporter cells | Email us | |
cell line of your choice | Email us |
References
- Martin LJ. Prog Mol Biol Transl Sci. 2012;107:355-415.
- Martin LJ. Pharmaceuticals (Basel). 2010;3(4):839-915.
- Chen K, Northington FJ, Martin LJ. Brain Struct Funct. 2010 Mar;214(2-3):219-34.
- Palomo GM, Manfredi G. Brain Res. 2015 May 14;1607:36-46.
- Dykens JA, Jamieson JD, Marroquin LD, Nadanaciva S, Xu JJ, Dunn MC, Smith AR, Will Y. Toxicol Sci. 2008 Jun;103(2):335-45.
- Dykens JA, Will Y. Drug Discov today. 2007 Sep; 12 (17-18): 777-85.