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CLS3473

Corning® Costar® Ultra-Low Attachment Multiple Well Plate

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

Synonym(s):

24 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

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 3473

size

24 well

surface area

1.9 cm2 , cell growth area (cm2)

well volume

3.4 mL

well working volume

0.38-0.57 mL

wells

24 wells

color

clear

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.

Certificates of Analysis (COA)

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Maxine Umeh-Garcia et al.
Cancer research, 80(3), 418-429 (2019-11-07)
miR-127 is downregulated in breast cancer, where it has been shown to suppress the proliferation, migration, and invasion of breast cancer cells. In triple-negative breast cancer (TNBC), miR-127 downregulation correlates with decreased disease-free and overall patient survival. Tumor suppressor miRNAs
Jin-A Lee et al.
Journal of cellular physiology, 236(5), 3946-3962 (2020-11-10)
The epigenome has an essential role in orchestrating transcriptional activation and modulating key developmental processes. Previously, we developed a library of pyrrole-imidazole polyamides (PIPs) conjugated with suberoylanilide hydroxamic acid (SAHA), a histone deacetylase (HDAC) inhibitor, for the purpose of sequence-specific

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