The largest database of trusted experimental protocols

Firefly luciferase

Manufactured by Takara Bio
Sourced in United States

Firefly luciferase is an enzyme derived from the firefly that catalyzes a bioluminescent reaction. It is commonly used in research applications as a reporter gene to monitor gene expression and activity.

Automatically generated - may contain errors

2 protocols using firefly luciferase

1

Dual Luciferase Reporter Assay in HEK293T Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
HEK293T cells were seeded at a density of 5 x 104 cells per well in 24-well plates overnight. Cells were then transfected with the experimental reporter plasmid pNF-κB-Luc (Firefly luciferase, Clontech, Mountain View, CA, USA), pIL8-Luc and the internal control plasmid pRL-TK (Renilla luciferase, Clontech), as well as other plasmids as described in the figure legend and our previous study.42 (link) When appropriate, cells were treated with PMA (79346, MilliporeSigma), TNF-α (300-01A, PeproTech) or IL-1β (200-01B, PeproTech). Enzyme activity was measured using the Dual Luciferase reporter assay kit (E1910, Promega) according to the manufacturer’s instructions.
+ Open protocol
+ Expand
2

NF-κB Signaling Pathway Regulation

Check if the same lab product or an alternative is used in the 5 most similar protocols
NF-κB-dependent reporter gene plasmid, pGL4.32[luc2P/NF-κB-RE/Hygro] (abbreviated to NF-κB-LUC hereafter), containing five copies of an NF-κB response element driving transcription of a destabilised form of Firefly Luciferase was purchased from Clontech. Control luciferase reporter gene containing only a minimal promoter (minP-LUC) was described previously [33 (link)]. Expression plasmid pCMV-p65, which expresses the RelA/p65 subunit of NF-κB, was a gift from Matthew Vincenti (Dartmouth Medical School, Lebanon, NH). Plasmid pDC515:mDIA-CT expressing a constitutively active nuclear mouse mDIA was made by subcloning the F1F2+C fragment of mDIA1 from pEF-mDIA-F1F2+C plasmid (a generous gift from John Copeland and described previously [39 (link)] into the BamH1 and Sal1 sites of pDC515 (Microbix). Recombinant adenoviral vector expressing an NLS-tagged polymerisation defective mutant of β-actin (Ad:NLS-ActinR62D) and control adenoviral vector lacking a transgene (Ad:Control) have been described previously [37 (link)]. Plasmid expressing exportin6 (XPO6) was described previously [37 (link)]. Silencer select siRNA for IPO9 and CFL1 were purchased from Invitrogen Life Technologies.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!