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Blue-Ribbon Poly A+ RNA and Total RNA
Rapid-Screen Arrayed cDNA Library Panels
cDNA Libraries
Molecular Tools
Millenium™ RNA Marker
Quanti-Ladder™ DNA Marker
Rapid-Load™ PCR Loading Dye
PrecisionShuttle ORF Vector System

OriGene cDNA clones in recent publications
Early Changes in Cytochrome P450s and Their Associated Arachidonic Acid Metabolites Play a Crucial Role in the Initiation of Cardiac Hypertrophy Induced by Isoproterenol Drug Metab. Dispos. Aug 2015 [CYP2J2]

Theaflavin-3,3'-digallate, a black tea polyphenol, stimulates lipolysis associated with the induction of mitochondrial uncoupling proteins and AMPK–FoxO3A–MnSOD pathway in 3T3-L1 adipocytes Journal of Functional Foods Aug 2015 [SOD2]

A New Versatile Immobilization Tag Based on the Ultra High Affinity and Reversibility of the Calmodulin-Calmodulin Binding Peptide Interaction J. Mol. Biol. Jul 2015 [CALM1]

Andrographolide inhibits the migration, invasion and matrix metalloproteinase expression of rheumatoid arthritis fibroblast-like synoviocytes via inhibition of HIF-1a signaling Life Sci. Jul 2015 [HIF1A]

View All Citations >>


Rapid-Load PCR Loading Dye is a 5x sample loading dye that is added to a PCR mix before amplification. The presence of Rapid-Load in the PCR mix will not interfere with the performance of the overall reaction. After the PCR is finished, the reaction products can be directly loaded in an agarose gel with no addition of standard loading dye necessary. This product can be used in PCR amplifications containing standard plasmid DNA, genomic DNA or bacterial colonies. It is also ideal for use with multiple samples such as when performing a 96-well PCR.

  • No PCR reaction interference
  • Load PCR samples directly on gel
  • Ideal for 96-well PCR

Rapid-Load PCR Loading Dye is red in color making it easy to load on agarose gels and track during electrophoresis. The red dye migrates at 1.4 kbp in a 1% agarose gel with 1x TAE running buffer. Fig.1 shows PCR amplification of human ?-actin from plasmid DNA, transformed bacterial colonies, and genomic DNA. Each reaction was performed in duplicate in the presence (+) or absence (-) of Rapid-Load.

RL Fig 1



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