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Merck

M3812

Sigma-Aldrich

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

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About This Item

UNSPSC Code:
41122107
NACRES:
NB.15

material

cyclic olefin copolymer (COC)
cyclic olefin copolymer (COC)
flat bottom clear cyclic olefin copolymer (COC) wells (cycloolefine)

sterility

non-sterile

feature

lid: no
skirt (F-bottom)

packaging

case of 40 ea (internal packs of 10)

manufacturer/tradename

Greiner 655801

size

96 wells

working volume

340 μL

binding type

non-treated surface

General description

UV-Star® 96W Microplate, well working volume 25-370 μL; total well volume 392 μL.

Compatible with Molecular Devices SPECTRAmax 190 and 250 plate readers.
  • 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)

Other Notes

96 well flat (F) μClear® bottom; microplate, chimney well, no lid, alphanumeric well coding, length: 127.76 mm; width: 85.48 mm; curvature approx. 200 μm

Suitability

Superior UV transparency with an expanded optical window down to 230 nm. Ideal for measurements of DNA and protein concentrations at 260 nm or 280 nm, respectively. Ideal alternative to expensive and fragile quartz glass plates. Clear bottoms allow for monitoring thru the plate bottom. Free of detectable DNase/RNase, human DNA and pyrogens.

Legal Information

μClear is a registered trademark of Greiner Bio-One GmbH
UV-Star is a registered trademark of Greiner Bio-One GmbH

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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