

744945.1 · 1 x 96 Preps
Takara · Cat: 744945.1
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Manufacturer product page
takarabio.com/products/nucleic-acid-purification/genomic-dna...
Description
NucleoMag DNA Food is designed for rapid manual or automated small-scale isolation of genomic DNA from up to 200 mg of food or feed samples of plant or animal origin, with typical yields ranging from 0.110 mug of pure DNA. The procedure is based on reversible adsorption of nucleic acids to paramagnetic beads under appropriate buffer conditions. Magnetic separation can be performed either manually using the NucleoMag SEP magnetic separator or on an automated platform using standard liquid handling instruments and magnetic separators. Manual preparation of 96 samples in parallel can be completed in approximately 2 hours using NucleoMag SEP. Automated preparation of 96 samples can be completed in less than 2 hours depending on the configuration of the automation platform and the separator being used. Cat. # 744945.1 includes sufficient quantities of reagents and beads for processing of 96 samples. Our products are to be used forResearch Use Only. They may not be used for any other purpose, including, but not limited to, use in humans, therapeutic or diagnostic use, or commercial use of any kind. Our products may not be transferred to third parties, resold, modified for resale, or used to manufacture commercial products or to provide a service to third parties without our prior written approval. Back Back NucleoMag DNA Food procedure. Back NucleoMag DNA Food can be used to isolate DNA from various food sample types.With NucleoMag DNA Food, a wide variety of food samples can be used as inputs for DNA isolation. For each sample type included in the graph, sample homogenization and lysis were performed manually, whereas DNA isolation was automated using a KingFisher Flex. The presence of DNA in the resulting eluates was determined using qPCR. Back Product comparison demonstrates superior performance of NucleoMag DNA Food.DNA was extracted from each of the indicated sample types in parallel using NucleoMag DNA Food and competitor kit P. For each extraction, sample homogenization and lysis were performed manually, whereas DNA isolation was automated using a KingFisher Flex. The presence of DNA in the resulting eluates was determined using qPCR. For each sample type processed, NucleoMag DNA Food provided superior performance relative to kit P, as indicated by the lower CTvalues for the DNA samples obtained with NucleoMag DNA Food.







