CLS3635
Corning® UV-Transparent Microplates
flat bottom clear, polystryrene, pkg of 50 ea, non-sterile, lid: no
Sinónimos:
96 multiwell plate, 96 well UV plate, 96 well UV/VIS plate, 96 well microplate, 96 well microtiter plate, 96 well plate
About This Item
Productos recomendados
material
clear acrylic copolymer plate
flat bottom clear
round clear wells
sterility
non-sterile
feature
lid: no
skirt
polystryrene
packaging
case of 50
pkg of 50 ea
manufacturer/tradename
Corning 3635
well volume
370 μL
well working volume
75-200 μL
wells
96 wells
color
clear
suitability
suitable for (protein and/or nucleic acid concentrations; UV/VIS applications)
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General description
Corning 96 well UV plates have a UV-transparent well bottom that is ideal for determining protein and/or nucleic acid concentrations.
- Certified for low background and consistent performance at 260 and 280 nm
- Certified DNase- and RNase-free
- UV-transparent bottom is molded directly to an acrylic base for greater strength and maximum leak resistance
- Total well volume: 360 μL; recommended working volumes of 75 to 200 μL
- Lids are available separately
Legal Information
Certificados de análisis (COA)
Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»
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Protocolos
Assays that predict passive absorption of orally administered drugs have become increasingly important in the drug discovery process. As previously described by Faller and Kansy such assays provide rapid, low cost and automation friendly methods to measure a compound’s passive permeability.
Assays that predict passive absorption of orally administered drugs have become increasingly important in the drug discovery process. As previously described by Faller and Kansy such assays provide rapid, low cost and automation friendly methods to measure a compound’s passive permeability.
Assays that predict passive absorption of orally administered drugs have become increasingly important in the drug discovery process. As previously described by Faller and Kansy such assays provide rapid, low cost and automation friendly methods to measure a compound’s passive permeability.
Assays that predict passive absorption of orally administered drugs have become increasingly important in the drug discovery process. As previously described by Faller and Kansy such assays provide rapid, low cost and automation friendly methods to measure a compound’s passive permeability.
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