M3812
Greiner UV-Star® 96 well plates
flat bottom clear cyclic olefin copolymer (COC) wells (cycloolefine)
Sinónimos:
96 multiwell plates, 96 well microplates, 96 well microtiter plates, 96 well plates
About This Item
cyclic olefin copolymer (COC)
flat bottom clear cyclic olefin copolymer (COC) wells (cycloolefine)
skirt (F-bottom)
Productos recomendados
Materiales
cyclic olefin copolymer (COC)
cyclic olefin copolymer (COC)
flat bottom clear cyclic olefin copolymer (COC) wells (cycloolefine)
esterilidad
non-sterile
Características
lid: no
skirt (F-bottom)
envase
case of 40 ea (internal packs of 10)
fabricante / nombre comercial
Greiner 655801
tamaño
96 wells
volumen de trabajo
340 μL
tipo de unión
non-treated surface
Categorías relacionadas
Descripción general
- Ultraviolet transparent multiwell plates from Greiner
- Highly recommended for measurements of DNA and protein concentrations at 260 nm or 280 nm, respectively
- No need for expensive and fragile quartz glass plates
- UV transparent to 200 nm
- Packs of 10
- 40/case (4 x 10 packs)
Compatible with Molecular Devices SPECTRAmax 190 and 250 plate readers.
Otras notas
Idoneidad
Información legal
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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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