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CLS3470

Corning® Transwell® 24 well plates

0.4 μm pore size, Tissue Culture (TC)-treated surface clear polystyrene plate, round wells, polyester membrane (Polyethylene Terephthalate (PET), flat bottom wells clear sterile, case of 48, pack of 12

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Synonym(s):
cell culture inserts, plate inserts, tissue culture dishes, tissue culture plates
UNSPSC Code:
41122107
NACRES:
NB.13

product name

Corning® Transwell® polyester membrane cell culture inserts, 6.5 mm Transwell with 0.4 μm pore polyester membrane insert, TC-treated, sterile, 48/cs

material

clear polystyrene plate
flat bottom wells clear
polyester membrane (Polyethylene Terephthalate (PET)
round wells

sterility

sterile

feature

lid
skirt

packaging

pack of 12
case of 48

manufacturer/tradename

Corning 3470

insert working volume

0.1 mL

membrane diam.

6.5 mm

membrane thickness

10 μm

size

24 wells

surface area

0.33 cm2 , cell growth area

well working volume

0.6 mL

color

clear

pore size

0.4 μm

binding type

Tissue Culture (TC)-treated surface

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General description

  • 10μm thick transparent polyester membrane
  • Treated for optimal cell attachment
  • Packaged 12 inserts in a 24 well plate, 4 plates per case
  • Excellent visibility under phase contrast microscopy
  • Sterilized by gamma radiation
Transwell cell culture inserts are convenient, easy-to-use permeable support devices for the study of both anchorage-dependent and anchorage-independent cell lines They feature a 10 mm, thin, microscopically transparent polyester membrane that is tissue culture treated for optimal cell attachment and growth.

Provides excellent cell visibility under phase contrast microscopy and allows assessment of cell viability and monolayer formation.

Legal Information

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

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Rho kinase (ROCK) is associated with VEGF-driven angiogenesis, as well as with inflammation and fibrosis. Therefore, the effect of AMA0428, a novel ROCK inhibitor, was studied in these processes, which highly contribute to the pathogenesis of neovascular AMD. The effect

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