D-LUX Assays












Nucleic Acid Amplification & Expression Profiling

D-LUX™ Gene Expression Assays

 D-LUX™ Gene Expression Assays use the latest generation of LUX™ (Light Upon eXtension) qPCR detection technology that combines robust chemistry with optimized bioinformatics to deliver the most sensitive, specific, and cost-effective detection method available for qPCR/qRT-PCR. With the D-LUX™ Detection Platform, you can:

  • Quantitate 10 or fewer copies with a dynamic range of up to eight orders of magnitude
  • Perform melting curve analysis to distinguish genuine amplicons from primer-dimers and other artifacts
  • Perform quantitation on any real-time instrument platform
  • Multiplex up to 3 targets per reaction
 How D-LUX™ Detection Technology Works

D-LUX™ detection technology uses one primer labeled with a single fluorophore and a corresponding unlabeled primer, both custom-synthesized according to the target of interest. Typically 20-30 bases in length, LUX™ Primers are designed with a fluorophore near the 3´end in a hairpin structure. This configuration intrinsically renders fluorescence quenching capability, making a separate quenching moiety unnecessary. When the primer becomes incorporated into the double-stranded PCR product, the fluorophore is de-quenched, resulting in a significant increase in fluorescent signal (Figure 1).
  Assay Design Assay Validation Species Dye Labels
Certified LUX™ Assays Pre-Designed Functional Infectious Diseases FAM
Reference Genes: multiple species FAM, JOE
D-LUX™ Select Gene Expression Assays Pre-Designed In silico Human, Mouse, Rat FAM, JOE, Alexa Fluor 546
Custom D-LUX™ Assays Customer Designed Online   Any FAM, JOE, Alexa Fluor 546
D-LUX™ Design and Validation Service Designed by Invitrogen Scientists Functional Any FAM, JOE, Alexa Fluor 546
Combine the best of probe-based and SYBR® Green detection

The D-LUX™ Detection Platform offers the sensitivity, specificity and dynamic range of TaqMan® probes, while providing the ease-of-use, cost-effectiveness and melting curve analysis capability of SYBR Green (Table 1).

Table 1—Comparison of real-time detection platforms


  TaqMan® Probes Molecular Beacons SYBR® Green 1 LUX™ Primers
Sensitivity ••• ••• •••
Dynamic range ••• ••• •••
Specificity ••• ••• •••
Multiplexing •• •• N/A •••
Melting curve analysis N/A N/A ••• •••
Ease of design ••• •••
Cost ••• •••