Real Time PCR Assays and Arrays - Pages 3

The Applied Biosystems™ Mouse ACTB (actin, beta) Endogenous Control (VIC™ ⁄ MGB Probe, Primer Limited) is intended as an endogenous control. It allows relative gene expression quantification in cDNA samples when it is used with other gene expressio

Applied Biosystems™ Protein Thermal Shift™ kits allow users to employ a dye that binds to exposed hydrophobic residues to monitor the thermal stability of proteins using a real-time PCR instrument in order to identify buffer conditions that stabilize the

Applied Biosystems™ Protein Thermal Shift™ kits allow users to employ a dye that binds to exposed hydrophobic residues to monitor the thermal stability of proteins using a real-time PCR instrument in order to identify buffer conditions that stabilize the

The Applied Biosystems™ TaqMan™ hPSC Scorecard™ Kit 384w enables verification of trilineage differentiation potential for both human ES and iPS cell lines. The 384-well plate contains four sets of 94 predefined TaqMan™ Gene Expression assays (including e

The Applied Biosystems™ TaqMan™ hPSC Scorecard™ Kit 2 x 96w FAST enables verification of pluripotency and determination of lineage bias for both ES and iPS cell lines. Each of the two 96-well plates contains 94 predefined TaqMan™ Gene Expression assays (

The Applied Biosystems™ TaqMan™ hPSC Scorecard™ Panel 384w enables verification of pluripotency and determination of lineage bias for both human ES and iPS cell lines. The 384-well plate contains four sets of 94 predefined TaqMan™ Gene Expression assays

The Applied Biosystems™ TaqMan™ hPSC Scorecard™ Panel 2 x 96w FAST enables verification of pluripotency and determination of lineage bias for both ES and iPS cell lines. Each of the two 96-well plates contains 94 predefined TaqMan™ Gene Expression assays

The enzyme concentration, ionic strength, and the pH of the TaqMan™ Protein Fast Master Mix are optimized for the amplification of ligated oligonucleotide target sequences prepared using TaqMan™ Protein Assay reagents. The DNA polymerase included in the

Uracil DNA Glycosylase (uracil-N-glycosylase) removes uracil residues from the sugar moiety of single- and double-stranded DNA without destroying the phosphodiester backbone, preventing its use as a hybridization target or as a template for DNA polymeras