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LUC1

Luciferase Reporter Gene Detection Kit

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About This Item

NACRES:
NA.84
UNSPSC Code:
12352207
Usage:
 kit sufficient for 100 assays
Storage temp.:
−70°C
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usage

 kit sufficient for 100 assays

Quality Level

storage temp.

−70°C

General description

Firefly luciferase is one of the most utilized reporter genes for the study of gene expression. It is an extremely sensitive, rapid, and easy-to-use reporter gene. The chemiluminescent reaction catalyzed by luciferase is one of the most sensitive analytical tools for measuring gene expression. The luciferase substrate contains coenzyme A for increased and sustained luminescence compared to conventional methods. This eliminates the need for automated luminometer injection of the substrate and allows analysis by photographic film or scintillation counting. The lysis buffer contains polymyxin B which further enhances the signal and eliminates lysozyme treatment and freeze-thawing of cells. Cell lysis buffer is compatible with β-galactosidase assays. The enzyme encoded by the luciferase reporter gene catalyzes the oxidation of D-luciferin in the presence of ATP, oxygen, and Mg2+. The fluorescent product is quantified to measure its activity.


pictograms

CorrosionEnvironment

signalword

Danger

Storage Class

10 - Combustible liquids

flash_point_f

Not applicable

flash_point_c

Not applicable

wgk

WGK 3

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 2 - ED ENV 1 - Eye Dam. 1



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Articles

Firefly luciferase is a sensitive reporter for gene studies due to its absence in mammalian cells or tissues.


Paola Monti et al.
Scientific reports, 10(1), 18427-18427 (2020-10-30)
Chronic lymphocytic leukaemia (CLL) is characterised by a heterogeneous clinical course. Such heterogeneity is associated with a number of markers, including TP53 gene inactivation. While TP53 gene alterations determine resistance to chemotherapy, it is not clear whether they can influence
Stephen T Smale
Cold Spring Harbor protocols, 2010(5), pdb-pdb (2010-05-05)
When a transient or stable transfection assay is developed for a promoter, a primary objective is to quantify promoter strength. Because transfection efficiency in such assays can be low, promoters are commonly fused to heterologous reporter genes that encode enzymes
Jaya Mishra et al.
Journal of the American Society of Nephrology : JASN, 14(10), 2534-2543 (2003-09-30)
Acute renal failure (ARF) secondary to ischemic injury remains a common and potentially devastating problem. A transcriptome-wide interrogation strategy was used to identify renal genes that are induced very early after renal ischemia, whose protein products might serve as novel



Global Trade Item Number

SKUGTIN
LUC1-1KT04061833967263