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NACRES:
NB.22
UNSPSC Code:
41122107
Material:
natural polypropylene
polypropylene
polypropylene
round bottom natural wells
polypropylene
polypropylene
round bottom natural wells
Size:
96 wells
Sterility:
non-sterile
Binding type:
non-treated surface
Feature:
lid: no
high flange design
high flange design
产品名称
Nunc® MicroWell™ 96 孔聚丙烯板, 96 well plate, polypropylene, natural, round bottom, 500uL/well, non sterile, 120/cs
material
natural polypropylene
polypropylene
polypropylene
round bottom natural wells
sterility
non-sterile
feature
lid: no
high flange design
packaging
case of 120 ea (internal packs of 10)
manufacturer/tradename
Nunc 267245
plate L × W
128 mm × 86 mm
size
96 wells
well maximum volume
500 μm
working volume
500 μL
binding type
non-treated surface
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Application
适用于:化合物存储、液相分析、库存储、样品运输和存储、筛选、样品收集、组合化学
Features and Benefits
- Shared wall design increases the well volume.
- Wider wells and rounded bottom improve mixing.
- Conical bottom well for optimal sample recovery.
- Black and white plates available for fluorescent- and luminescent-based applications.
- Low binding polypropylene for homogeneous assays and storage.
- Compatible with robotics and automated systems.
- Polypropylene resin is resistant to most chemicals, solvents and alcohols.
- Minimal binding of molecules with hydrophilic moities.
- Non-toxic.
- Products come without lids.
General description
Achieve complete sample recovery with Nunc® 96-well polypropylene MicroWell™ Plates, which are the ideal storage plate as polypropylene has a lower binding capacity so proteins or DNA will not bind. Withstands temperatures from -80° to +121°C. Available in a variety of colors for quick identification of storage plates.
Legal Information
MicroWell is a trademark of Thermo Fisher Scientific or its subsidiaries
Nunc is a registered trademark of Thermo Fisher Scientific or its subsidiaries
Alysha G Elliott et al.
Nature communications, 11(1), 3184-3184 (2020-06-25)
Peptide antibiotics are an abundant and synthetically tractable source of molecular diversity, but they are often cationic and can be cytotoxic, nephrotoxic and/or ototoxic, which has limited their clinical development. Here we report structure-guided optimization of an amphipathic peptide, arenicin-3
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