Z717266
Nunc® 96 DeepWell™ plate, non-treated
maximum volume 2 mL, non-sterile, round bottom natural polypropylene wells
Synonym(s):
96 deepwell culture plate, 96 deepwell plate
About This Item
material
natural polypropylene
polypropylene
round bottom natural polypropylene wells
sterility
non-sterile
feature
lid: no
packaging
pack of 5 ea
manufacturer/tradename
Nunc 278752
maximum volume
2 mL
plate L × W
128 mm × 86 mm
size
96 wells , deep wells
well maximum volume
2 μm
well volume
2 mL
working volume
1.9 mL
color
natural
suitability
suitable for (sample collection, storage, combinatorial chemistry and library applications)
binding type
non-treated surface
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General description
- Unique low design with shared well technology for increased well volume
- 1.3 and 2.0 mL volume capacity
- Optimum storage capacity and improved mixing
- Round well shape reduces liquid retention
- Well cap available for safe storage – minimal protrusion into each well
- Ideal for sample collection, storage, combinatorial chemistry and library applications
- Resistant to most chemicals, solvents and alcohols used in combinatorial chemistry
- Widely used for bacterial and yeast growth
- Easy-to-use with automatic sample handling instruments
- Alpha-numeric grid for quick sample identification
- Ideal for sample collection, storage, and combinatorial chemistry library applications
- Sealable with well caps and sealing tape
- Ideal as collection plates for Nunc Filter Plates
Legal Information
Certificates of Analysis (COA)
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The conversion of clinical methods to LC/MS/MS offers advantages; however, is accompanied by a few limitations, notably interference effects from the endogenous sample matrix.
The conversion of clinical methods to LC/MS/MS offers advantages; however, is accompanied by a few limitations, notably interference effects from the endogenous sample matrix.
The conversion of clinical methods to LC/MS/MS offers advantages; however, is accompanied by a few limitations, notably interference effects from the endogenous sample matrix.
The conversion of clinical methods to LC/MS/MS offers advantages; however, is accompanied by a few limitations, notably interference effects from the endogenous sample matrix.
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