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Contamination ,detection, assays can be used in a broad range of applications to measure contamination in a variety of sample content from fermentation supernatants and purification processes to biochemical preparations such as serum and other bodily fluids. They also measure the presence of host cell ,DNA, as well as other ,DNA, that might have been introduced during the biopharmaceutical ...

The AlphaLISA^® Host Cell Residual ,DNA Detection Kit, is designed for ,detection, and quantitation of ,DNA, contaminants in cell culture supernatants using a homogeneous (no-wash steps, no separation steps) assay. This ,kit, can be used with ,DNA, from different prokaryotic and eukaryotic species.

This quantitative PCR (qPCR)-based ,kit,—part of the resDNASEQ® E. coliResidual ,DNA, Quantitation System—enables highly sensitive quantitation of host cell ,DNA, from E. coliexpression systems, typically in less than 4 hours. The ,kit, is part of an integrated system that includes sample preparation, TaqMan® Assay and master mix, standard ,DNA,, instrument, and software.

QPCR ,Kit,, ,DNA,, Universal meat ,detection, (with Mastermix) TKIT07001 QPCR ,Kit,, ,DNA,, Bifidobacterium bifidum (without Mastermix) TKIT07001M QPCR ,Kit,, ,DNA,, Bifidobacterium bifidum (with Mastermix) TKIT07002 QPCR ,Kit,, ,DNA,, Bacillus cereus E33 ...

The technology is already in use for ,detection, of ,DNA, methylation biomarkers in fields like forensics, and for investigating challenging ,DNA, materiel sources as liquid biopsies and FFPE tissues. MethylDetect offers ready-to-use ,kits, for ,detection, of aberrant gene methylation.

ddPCR CHO and E. coli Residual ,DNA, Quantification ,Kits, enable highly sensitive and precise ,detection, and quantification of host cell ,DNA, without a standard curve. The ddPCR CHO Residual ,DNA, Quantification ,Kit, can reliably detect as little as 1 fg of ,DNA, with a limit of quantification (LOQ) of ≤15 fg per 20 µl reaction and a linear range of 3 fg–3 pg.

The Apoptotic ,DNA, Ladder ,Detection Kit, I provides an easy and sensitive means for detecting ,DNA, fragmentation in apoptotic cells. The method requires less than 90 minutes to prepare the ,DNA,, without the need for extraction or columns. ,DNA, fragmentation can then …

DNA, was purified from hair of 3 brown horses and analyzed for coat-color genotypes using the MSH and ASIP PCR systems. [A] MSH PCR products were digested with TaqI. Horses 1 and 3 were identified as Ee heterozygotes, carrying the recessive e allele for red coat color.[B] Analysis of ASIP PCR products identify horses 1 and 2 as Aa heterozygotes, carrying the recessive a allele for black coat color.

Exalpha’s ,DNA, Fragmentation ,Detection Kit, components are shipped on cold pack. Upon receipt, store ,kit, at -20°C in a non-frost-free freezer. For long term storage, it is recommended that you aliquot and freeze the TdT Enzyme (Component 4), TdT Labeling Reaction Mix (Component 3), and 25x Streptavidin-HRP Conjugate (Component 7) at -20 °C.