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CLS3614

Corning® 96 Well Special Optics Microplate

flat bottom clear, black polystyrene, Tissue Culture (TC)-treated surface, bag of 25, sterile

Synonym(s):

96 multiwell plates, 96 well microplates, 96 well microtiter plates, 96 well plates, optically clear flat bottom plates

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About This Item

UNSPSC Code:
41121800
NACRES:
NB.24

material

black polystyrene
black/clear bottom polystyrene plate
clear bottom
flat bottom clear

sterility

sterile

feature

lid: no
skirt
 plate format: 96 well special optics

packaging

case of 100
bag of 25

manufacturer/tradename

Corning 3614

maximum volume

360 μL

size

96 wells

surface area

0.32 cm2 , cell growth area

cell growth area

cell growth area

working volume

200 μL

suitability

suitable for (optically clear flat well bottom permits direct microscopic viewing)

binding type

Tissue Culture (TC)-treated surface

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General description

  • Ultra thin, optically clear flat well bottom permits direct microscopic viewing, resulting in lower background fluorescence and enabling readings down to 340nm
  • Opaque walls to prevent well-to-well crosstalk
  • Can be used for both top and bottom reading instruments
  • Flat bottoms with 360μL total volume
  • Recommended working volumes of 75 to 200μL
  • Sterilized by gamma radiation and certified nonpyrogenic
  • Without lids
  • Bulk packed 25 per bag
Corning® 96 Well Special Optics Plates

The 96 well special optics plates have black, opaque walls, and ultra thin flat clear bottoms that permit direct microscopic viewing and improved optical performance in fluorescent-based assays.

Legal Information

Corning is a registered 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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Nathan D Trinklein et al.
mAbs, 11(4), 639-652 (2019-01-31)
T-cell-recruiting bispecific antibodies (T-BsAbs) have shown potent tumor killing activity in humans, but cytokine release-related toxicities have affected their clinical utility. The use of novel anti-CD3 binding domains with more favorable properties could aid in the creation of T-BsAbs with

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