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Bioluminescence Assays and Reagents

Bioluminescence Assays and Reagents

Luciferase vectors, cell lysis buffers, signal enhancers, transfection reagents, assay kits, and other associated products for optimal luciferase reporter assay performance.
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46 – 60 of 337 results
46

Promega pGL4.54[luc2/TK] Vector

Vectors are used as controls in dual-luciferase assays where Renilla or NanoLuc luciferase is the experimental reporter.

47

Promega Nano-Glo™ Dual-Luciferase™ Reporter Assay/pGL4.54[luc2/TK] Bundle

The Nano-Glo™ Dual-Luciferase Reporter (NanoDLR) Assay System is a homogeneous reagent system that allows you to sequentially detect the activities of firefly (Photinus pyralis) luciferase and NanoLuc luciferase (Nluc) from a single sample.

48

Promega pNL3.2[NlucP/minP] Vector

NanoLuc (Nluc) luciferase is a small enzyme (19.1kDa) engineered for optimal performance as a luminescent reporter. The Vectors offer a minimal promoter for cloning response elements of interest.

49

Promega pNL1.1.PGK[Nluc/PGK] Vector

The promoter-driven NanoLuc (Nluc) control vectors can be used to co-transfect with experimental firefly luciferase vectors when using the Nano-Glo™ Dual-Luciferase Reporter (NanoDLR) Assay System.

50

Promega pNLF1-N [CMV/Hygro] Vector

Generate N-Terminal Fusions with NanoLuc™ Enzyme. The pNLF1 Vectors use traditional cloning with a multiple cloning site (MCS) to generate N-terminal fusions to NanoLuc™ luciferase. All vectors contain a mammalian selectable marker to create a stable line.

51

Promega pGL4.53[luc2/PGK] Vector

Vectors are used as controls in dual-luciferase assays where Renilla or NanoLuc luciferase is the experimental reporter.

52

Promega pNLF1-secN [CMV/Hygro] Vector

Generate N-Terminal Fusions with N-Terminal Secreted NanoLuc™ Luciferase. The pNLF1 Vectors use traditional cloning with a multiple cloning site to generate N-terminal fusions to NanoLuc™ luciferase. All vectors contain a mammalian selectable marker to create a stable line.

53

Promega pNL3.2.CMV Vector

NanoLuc (Nluc) luciferase is a small bright luminescent reporter enzyme (19.1kDa) engineered for optimal performance. Use the pNL3.2.CMV Vector as a negative control in experiments measuring regulated changes in NanoLuc luciferase expression.

54

Promega Nano-Glo™ Dual-Luciferase™ Reporter Assay/pGL4.53[luc2/PGK] Bundle

The Nano-Glo™ Dual-Luciferase Reporter (NanoDLR) Assay System is a homogeneous reagent system that allows you to sequentially detect the activities of firefly (Photinus pyralis) luciferase and NanoLuc luciferase (Nluc) from a single sample.

55

Promega pNLF1-HIF1A [CMV/neo] Vector

NanoLuc Stability Sensors are ready-to-use vector systems that utilize the advantages of the NanoLuc luciferase reporter for stability studies of two key signaling proteins, HIF1A and NRF2, providing a way to directly measure the primary signaling event.

56

Promega pNLCoI2[luc2-P2A-NlucP/minP/Hygro] Vector

The pNLCoI Vectors comprise a second-generation coincidence reporter vector system that allow expression of both firefly luciferase (luc2) and NanoLuc Luciferase fused to a PEST destabilization domain (NlucP) from the same mRNA transcript.

57

Promega Nano-Glo HiBiT Lytic Detection System, 10 x 100ml

Accurately quantify Any HiBiT Tagged Protein Expressed in Cells in an antibody free, plate based method.

58

Promega QuantiLum™ Recombinant Luciferase

QuantiLum Recombinant Luciferase is a luciferase expressed from a cloned gene from the North American firefly (Photinus pyralis).

Content And Storage <-65°C
Concentration 10 to 15 mg/mL
59

Promega pFC32K Nluc CMV-neo Flexi™ Vector

Generate C-Terminal Fusions to NanoLuc™ Luciferase Reporter. The pFC32A and pFC32K Nluc CMV-neo Flexi™ Vectors use a directional cloning method based on two rare-cutting restriction enzymes, SgfI and PmeI, and contain a mammalian selectable marker to create a stable line.

60

Promega pFC32A Nluc CMV-Hygro Flexi™ Vector

Generate C-Terminal Fusions to NanoLuc™ Luciferase Reporter. The pFC32A and pFC32K Nluc CMV-neo Flexi™ Vectors use a directional cloning method based on two rare-cutting restriction enzymes, SgfI and PmeI, and contain a mammalian selectable marker to create a stable line.