GE10600003
Amersham™ Protran® Premium Western blotting membranes, nitrocellulose
pore size 0.45 μm, roll W × L 300 mm × 4 m, pkg of 1 ea
Synonym(s):
Western blotting membrane, 0.2 NC nitrocellulose membrane
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About This Item
UNSPSC Code:
41105339
NACRES:
NB.22
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packaging
pkg of 1 ea
manufacturer/tradename
Cytiva 10600003
roll W × L
300 mm × 4 m
pore size
0.45 μm pore size
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General description
Nitrocellulose blotting membrane, provides excellent sensitivity, resolution, and low background in fluorescence Western blotting detection applications.
Application
Amersham™ Protran® Premium Western blotting membranes, nitrocellulose may be used in:
- Western blotting
- Southern blotting
- Northern blotting
Features and Benefits
- Offers high binding capacity (162 - 180 μg IgG/cm2).
- Suitable for proteins of different molecular weights
- Unsupported, 100% pure nitrocellulose membrane is suitable for all ECL Western blotting systems and protein blotting applications.
- Popular precut sizes are available for laboratory application
- Provides excellent sensitivity, resolution and low background particularly when used with the fluorescence Amersham ECL Plex Western blotting detection system
Storage and Stability
Please be aware this product may be shipped 90 days before the expiration date. For more information on the batch specific expiration date, please contact technical service.
Legal Information
Amersham is a trademark of Cytiva
Protran is a registered trademark of Cytiva
Signal Word
Warning
Hazard Statements
Precautionary Statements
Storage Class Code
11 - Combustible Solids
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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Marina Aznaourova et al.
Proceedings of the National Academy of Sciences of the United States of America, 117(16), 9042-9053 (2020-04-04)
RNA has been proposed as an important scaffolding factor in the nucleus, aiding protein complex assembly in the dense intracellular milieu. Architectural contributions of RNA to cytosolic signaling pathways, however, remain largely unknown. Here, we devised a multidimensional gradient approach
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