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CLS9102

Corning® 96 well plates

Clear Flat Bottom Polystyrene, TC-Treated, Individually Wrapped, Sterile, 1 x 8 Stripwell

Synonym(s):

cell culture plate, stripwell, tissue culture plates, well plates

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About This Item

UNSPSC Code:
41122107
NACRES:
NB.15

material

clear bottom
clear wells
flat wells
polystyrene
polystyrene plate
round wells

description

growth area .32 cm2

sterility

sterile

feature

lid
skirt
1 x 8 Stripwell
plate format: 96 well standard

packaging

case of 100
pack of 25
case of 50 (individually wrapped)

manufacturer/tradename

Corning 9102

size

96 wells

well diam.

6.4 mm

well volume

360 μL
360 μL

well working volume

75-200 μL

binding type

Tissue Culture (TC)-treated surface

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Application

Corning® 96-well (1 x 8 Stripwell) is suitable for cell based assays.

Features and Benefits

  • 8 well strip plate, assembled 12 strips per plate
  • Egg-crate style strip holder allows each individual well to be positioned back into the plate once strip is broken
  • 1 x 8 strips are designed to fit only one way into the strip holder, to avoid the chance of misorientation
  • Flat bottom microplate with total well volume of 360 μL and recommended working volumes of 75 to 200 μL
  • Surface treated for optimal cell attachment and to improve the binding of difficult to attach cell lines
  • Individually wrapped with nonreversible lids containing condensation rings to reduce contamination
  • Microplates are sterilized and certified nonpyrogenic
  • Individual alphanumeric codes enable easy well identification

Legal Information

Corning is a registered trademark of Corning, Inc.
Stripwell is a 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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The Glucagon-like peptide 1 receptor (GLP-1R) is a well-established target for the treatment of type 2 diabetes and GLP-1R agonist-based therapies represent an effective approach which results in several GLP-1 analog drugs. However, the development of nonpeptidic agonist drugs targeting

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