NF-κB Luciferase Reporter Raw 264.7 Cell Line
NF-κB Luciferase Reporter Raw 264.7 Cell Line is a Raw 264.7 cell line expressing firefly luciferase driven by four copies of the NF-kB response element located upstream of the minimal TATA promoter. After activation by pro-inflammatory cytokines or stimulants of lymphokine receptors, endogenous NF-κB transcription factors bind to the DNA response elements, inducing transcription of the luciferase reporter gene. This cell line has been functionally validated and responds to TNFα and RANKL
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Media Required for Cell Culture
Name | Ordering Information |
Thaw Medium 11 | BPS Bioscience #79976 |
Growth Medium 11A | BPS Bioscience #79977 |
Materials Used in the Cellular Assay
Name | Ordering Information |
Mouse RANKL | R&D Systems #462-TEC-010 |
Mouse TNFα | R&D Systems #410-MT |
ONE-Step™ Luciferase Assay System | BPS Bioscience #60690 |
White clear-bottom 96-well cell culture plate | |
Luminometer |
The cell line has been screened to confirm the absence of Mycoplasma species.
The role of NF-κB (nuclear factor-κB) activation is well-characterized in canonical (classical) and noncanonical (alternative) signaling pathways of inflammation. Two major forms of innate immune sensors are Toll-like receptors (TLR) and NOD/CATERPILLAR proteins. Mutations in NOD2 (nucleotide-binding oligomerization domain-containing protein 2) have been linked to chronic autoinflammatory and autoimmune diseases, such as Crohn’s disease and Blaus syndrome. Studying the canonical and noncanonical NF-κB pathways and the influence of TLR pathways and NOD2 mutations can further our understanding of autoimmune regulation. Raw 264.6 is a murine macrophage cell line useful for studies involving immunoreactivity. The use of a luciferase reporter allows for easy read outs in cellular assays.
Peninnger, J. M., et al., 2006 Trends Mol. Med. 12(1):17-25.
Baeuerle, P.A., 1998 Curr Biol. 8(1):R19-R22.