Amplification primers are short, single-stranded nucleotide sequences that are complementary to a fragment of the DNA or RNA that a researcher wants to amplify or sequence. Prior to the PCR amplification process, a primer hybridizes with its complementary sequence on a single strand of DNA or RNA. The formation of a short, double-stranded sequence permits binding and activity by a polymerase enzyme, kick-starting the amplification process.
Hybridization probes are short, labeled, single-stranded nucleotide sequences that are complementary to a fragment of DNA or RNA that the researcher wants to detect. Probes may be labeled with fluorescent dyes, or other chemicals that permit rapid, quantitative detection. Probes function by hybridizing with a desired complementary sequence, the desired sequence may then be detected via the label associated with the probe. We offer you a wide variety of primers and probes. if you have any questions regarding our products, please contact our customer service via live chat, email, or phone.
Polymerase Chain Reaction, DNA Sequencing, cDNA Synthesis, DNA Amplification
Diesel, Hoppstädter, Hachenthal, Zarbock, Cavelius, Wahl, Thewes, Jacobs, Kraegeloh, Kiemer: "Activation of Rac1 GTPase by nanoparticulate structures in human macrophages." in: European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft für Pharmazeutische Verfahrenstechnik e.V, Vol. 84, Issue 2, pp. 315-24, 2013 (Pubmed)
cDNA Synthesis, DNA Sequencing, Polymerase Chain Reaction
Dunbar, Chekan, Cox, Burkhart, Nair, Mitchell: "Discovery of a new ATP-binding motif involved in peptidic azoline biosynthesis." in: Nature chemical biology, Vol. 10, Issue 10, pp. 823-9, 2014 (Pubmed)
Robinson, Murray: "Genetic variation of wheat streak mosaic virus in the United States Pacific Northwest." in: Phytopathology, Vol. 103, Issue 1, pp. 98-104, 2012 (Pubmed)
Catalog No. ABIN1536170
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Roush, Myrold, Burnham, And, Hughes: "Limits in virus filtration capability? Impact of virus quality and spike level on virus removal with xenotropic murine leukemia virus." in: Biotechnology progress, Vol. 31, Issue 1, pp. 135-44, 2015 (Pubmed)
Zhang, Majeed, Lagae, Peumans, Van Hoof, De Malsche: "Ion-pair reversed-phase chromatography of short double-stranded deoxyribonucleic acid in silicon micro-pillar array columns: retention model and applications." in: Journal of chromatography. A, Vol. 1294, Issue , pp. 1-9, 2013 (Pubmed)
Slocum, Burnham, Genest, Venkiteshwaran, Chen, Hughes: "Impact of virus preparation quality on parvovirus filter performance." in: Biotechnology and bioengineering, Vol. 110, Issue 1, pp. 229-39, 2012 (Pubmed)
Yang, Fortin, Richardson, Buckley: "Fused-core silica column ultra-performance liquid chromatography-ion trap tandem mass spectrometry for determination of global DNA methylation status." in: Analytical biochemistry, Vol. 409, Issue 1, pp. 138-43, 2010 (Pubmed)