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CLS3635

Corning® UV-Transparent Microplates

flat bottom clear, polystryrene, pkg of 50 ea, non-sterile, lid: no

Synonym(s):

96 multiwell plate, 96 well UV plate, 96 well UV/VIS plate, 96 well microplate, 96 well microtiter plate, 96 well plate

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About This Item

UNSPSC Code:
41121800
NACRES:
NB.24

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

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

Corning is a registered trademark of Corning, Inc.

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Thomas Boehm et al.
Inflammation research : official journal of the European Histamine Research Society ... [et al.], 69(9), 937-950 (2020-06-04)
To measure diamine oxidase (DAO) activity with high sensitivity in complex matrices like plasma or tissue extracts radioactive putrescine or horseradish peroxidase (HRP)/hydrogen peroxide (H2O2) coupling must be used. The use of radioactive material should be avoided and HRP/H2O2 coupling

Protocols

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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