EP022431081
Eppendorf® Protein LoBind tubes
capacity 1.5 mL, PCR clean, pkg of 100 ea (2 x 50ea)
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About This Item
UNSPSC Code:
41121703
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material
(push fit)
polypropylene cap
sterility
non-sterile
feature
PCR clean
packaging
pkg of 100 ea (2 x 50ea)
manufacturer/tradename
Eppendorf® 022431081
parameter
-18,000 × g max. RCF
capacity
1.5 mL
diam.
10.7 mm
color
clear
suitability
suitable for PCR
binding type
low binding surface
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General description
Protein LoBind Tubes, snap cap, Protein LoBind, 1.5 mL, PCR clean, colorless, 100 tubes (2 bags × 50 tubes)
- Eppendorf LoBind material ensures optimized sample recovery for improved assay results
- Free of surface coating (e.g., silicone) to minimize the risk of sample interference
- Lot-certified PCR clean purity grade: free of human DNA, DNase, RNase and PCR inhibitors
- Available in tube, microplate, and deepwell plate formats for easy-up scaling
- Precise lid sealing to minimize evaporation
Features and Benefits
Eppendorf Protein LoBind Tubes are specifically designed to ensure you get maximal protein recovery.
Legal Information
Eppendorf is a registered trademark of Eppendorf AG
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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Nikos Tsolakos et al.
Vaccine, 28(18), 3211-3218 (2010-03-02)
In this study, we evaluated the effect of the growth medium on the composition and immunogenicity of meningococcal outer membrane vesicle (OMV) vaccines after cultivation of the Norwegian serogroup B 44/76 vaccine strain in either Frantz' or modified Catlin-6 media
E I Trilisky et al.
Journal of chromatography. A, 1142(1), 2-12 (2007-01-24)
Purified viruses are used in gene therapy and vaccine production. Ion-exchange chromatography (IEC) is the most common method for large-scale downstream purification of viruses and proteins. Published IEC protocols provide details for specific separations but not general methods for selecting
Thandavarayan Kathiresan et al.
Methods in molecular biology (Clifton, N.J.), 493, 269-286 (2008-10-08)
Functional proteomics comprises a wide range of technologies for the identification of novel protein-protein interactions and biological markers. Studies of protein-protein interactions have gained from the development of techniques and technologies such as immunoprecipitation, preparative two-dimensional (2-D) gel electrophoresis for
M Yang et al.
International journal of pharmaceutics, 331(2), 176-181 (2006-11-28)
Salmon calcitonin (sCT) powders suitable for inhalation, containing chitosan and mannitol as absorption enhancer and protection agent, respectively, were prepared using a spray-drying process. The effect of chitosan on physicochemical stability of sCT in the dry powder was investigated by
Sharon N Finger et al.
Nucleic acids research, 36(4), 1260-1272 (2008-01-05)
Telomerase is a ribonucleoprotein enzyme that maintains chromosome ends through de novo addition of telomeric DNA. The ability of telomerase to interact with its DNA substrate at sites outside its catalytic centre ('anchor sites') is important for its unique ability
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