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CLS7007

Corning® Costar® Ultra-Low Attachment Multiple Well Plate

size 96 wells, round 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

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

polystyrene , round bottom clear , round wells

sterility

sterile

feature

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

manufacturer/tradename

Corning 7007

packaging

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

size

96 wells

surface area

0.32 cm2 , cell growth area (cm2)

well volume

330 μL

well working volume

75-200 μL

color

clear

suitability

suitable for (cell cuture)

binding type

(Ultra-Low Attachment)

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

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

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Benjamin Izar et al.
Nature medicine, 26(8), 1271-1279 (2020-06-24)
Malignant abdominal fluid (ascites) frequently develops in women with advanced high-grade serous ovarian cancer (HGSOC) and is associated with drug resistance and a poor prognosis1. To comprehensively characterize the HGSOC ascites ecosystem, we used single-cell RNA sequencing to profile ~11,000
Nina Marie Pedersen et al.
The Journal of cell biology, 219(8) (2020-06-02)
Cancer cells break tissue barriers by use of small actin-rich membrane protrusions called invadopodia. Complete invadopodia maturation depends on protrusion outgrowth and the targeted delivery of the matrix metalloproteinase MT1-MMP via endosomal transport by mechanisms that are not known. Here