BookTitleWATSON BIO LAB General Catalog
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WATSON BIO LAB General Catalog
Recover SamplesDirectly on PCR PlateSpace SavingSelect a preservation plateaccording to the sample typeCut out the necessary size ofpaper chip.Pick up the paper chipfrom tweezer hole.Push the paper chipsby tweezers etc.①Peel off the protection seal and place the paper chip into a container.②Put the solution into the container and stir. In the case of agar, rub the paper chip onto agar.It is very compact and space saving incomparison with preserving in tubessamples of liquid condition.Marking space on the plate andcompact body make sample storagemanagement easier.Because a protective agent is applied tothe paper chips of the "MicrobialPreservation Plate", it is very suitable fordesiccation of bacteria and yeast. Inaddition, the paper chips used in"Preservation Plate" which can preservenucleic acid and blood, do not containany reagents and salt. Thus, you can lateruse any desired solution.Paper chips can be putdirectly into thesolution to start PCR orin situ hybridization.Preservation Method Recovery Method①Let the paper chip absorb a liquid sample. A: For a liquid sample ※Solution volume per well 96 well→5 μL 3 well→50 μL 1 well→200 μL B: For a sample from agar②Dry the sample. ※Recommended dry time 96 well→60 minutes or more 3 ・ 1 well→90 minutes or more③Seal the plate with the protection seal and store it in room temperature.ABPreservation Plate Microorganisms and DNA can be preserved in a dry state!A new style of sample preservation.Note : When handling the specific pathogens, please act in accordance with the applicable laws and regulations in your country.Reduce Contamination RiskCompared to the traditional way ofrepeated samplings from the sametube, Preservation Plate (PVP) canreduce contamination risk by usingdifferent wells on the PVP and/orchanging the PVP sheet itselfdependent on the sample (Note: Only96 well PVP can be cut easily withscissors).1 well 3 well96well58 Preservation Plates Preservation Plates Preservation Plates