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Merck
CN

CLS3474

Corning® Costar® Ultra-Low Attachment Multiple Well Plate

size 96 well, flat bottom clear, pkg of (individually wrapped), pkg of (24/case), sterile, lid

Synonym(s):

96 multiwell plate, 96 well microplate, 96 well microtiter plate, 96 well plate, cell culture plate, tissue culture plate

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About This Item

UNSPSC Code:
41121800
NACRES:
NB.13
Material:
clear
flat bottom clear
polystyrene
round wells
Size:
96 well

Key Documents

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material

clear
flat bottom clear
polystyrene
round wells

sterility

sterile
sterile

feature

lid
lid
skirt
 plate format: standard
 well: flat bottom, clear

packaging

pack of 1 (individually wrapped w/ lid)
case of 24
pkg of (24/case)
pkg of (individually wrapped)

manufacturer/tradename

Corning 3474

size

96 well

surface area

0.32 cm2 , cell growth area (cm2)

well volume

360 μL

well working volume

75-200 μL

wells

96 wells

color

clear

suitability

suitable for (cell cuture)

binding type

(Ultra-Low Attachment)

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General description

Corning Costar Ultra-Low Attachment Multiwell Plates

  • Ultra-Low attachment plates feature a covalently bound hydrogel layer that effectively inhibits cellular attachment
  • Surface minimizes protein absorption, enzyme activation, and cellular activation
  • Surface is non-cytotoxic, biologically inert, and nondegradable
  • Nonreversible lids with condensation rings to reduce contamination
  • Individual alphanumerical codes for well identification
  • Uniform footprint for ease in stacking
  • Sterilized by gamma irradiation and certified nonpyrogenic

Legal Information

Corning is a registered trademark of Corning, Inc.
Costar is a registered trademark of Corning, Inc.

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Haitang Yang et al.
Cancers, 12(8) (2020-08-23)
Background: Malignant pleural mesothelioma (MPM) is driven by the inactivation of tumor suppressor genes (TSGs). An unmet need in the field is the translation of the genomic landscape into effective TSG-specific therapies. Methods: We correlated genomes against transcriptomes of patients'
Gianpaolo Zarletti et al.
Viruses, 12(11) (2020-11-12)
Knowledge of the antibody-mediated immune response to SARS-CoV-2 is crucial to understand virus immunogenicity, establish seroprevalence, and determine whether subjects or recovered patients are at risk for infection/reinfection and would therefore benefit from vaccination. Here, we describe a novel and
Shiny Amala Priya Rajan et al.
Acta biomaterialia, 106, 124-135 (2020-02-19)
Current drug development techniques are expensive and inefficient, partially due to the use of preclinical models that do not accurately recapitulate in vivo drug efficacy and cytotoxicity. To address this challenge, we report on an integrated, in vitro multi-organoid system

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