CLS8160
Corning® Costar® Spin-X® centrifuge tube filters
cellulose acetate membrane, pore size 0.22 μm, sterile
동의어(들):
centrifuge columns, centrifuge tube filters, desalting columns, tube filters
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
UNSPSC Code:
41104916
NACRES:
NB.11
eCl@ss:
32119210
Material:
cellulose acetate membrane, natural polypropylene cap, polypropylene housing, polypropylene tube
Pore size:
0.22 μm
Working volume:
500 μL
Sterility:
sterile
Packaging:
case of 96 units
material
cellulose acetate membrane, natural polypropylene cap, polypropylene housing, polypropylene tube
description
centrifuge style filter
sterility
sterile
feature
RCF 16,000 × g, RNase and DNase free
packaging
case of 96 units
manufacturer/tradename
Corning 8160
tube size
2.0 mL
working volume
500 μL
pore size
0.22 μm
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General description
These Costar® Spin-X® polypropylene microcentrifuge tube filters are available with Cellulose Acetate or Nylon membranes and 0.22 or 0.45 μm membrane pore sizes. The filter unit capacity is 500 μL.
- Cellulose acetate (CA) membranes provide fast flow rates and low protein binding
- Nylon (NY) membranes are naturally hydrophilic, surfactant-free and offer the lowest extractables
- Both CA and NY filter by centrifugation for removing bacteria, particles, or cells from liquids, HPLC sample preparation and DNA removal from agarose or acrylamide gels
- Use in any standard fixed-angle microcentrifuge rotor at RCF up to 16,000 × g
- Sterile and certified nonpyrogenic and DNase-/RNase-free
Application
Ideal for removing bacteria, particles, or cells from liquids, HPLC sample preparation and DNA removal from agarose or acrylamide gels.
Legal Information
Corning is a registered trademark of Corning, Inc.
Costar is a registered trademark of Corning, Inc.
SPIN-X is a registered trademark of Corning, Inc.
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Pathogens (Basel, Switzerland), 9(2) (2020-02-23)
Inactivated whole-virus vaccines are widely used for the control of foot-and-mouth disease (FMD). Their production requires the growth of large quantities of virulent FMD virus in biocontainment facilities, which is expensive and carries the risk of an inadvertent release of
Alita R Burmeister et al.
Proceedings of the National Academy of Sciences of the United States of America, 117(21), 11207-11216 (2020-05-20)
Bacteria frequently encounter selection by both antibiotics and lytic bacteriophages. However, the evolutionary interactions between antibiotics and phages remain unclear, in particular, whether and when phages can drive evolutionary trade-offs with antibiotic resistance. Here, we describe Escherichia coli phage U136B
Parvez Vora et al.
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