EP022431048
Eppendorf® DNA LoBind tubes
capacity 2.0 mL, PCR clean, pkg of 250 ea (5 x 50ea)
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UNSPSC Code:
41103037
To inquire about this product EP022431048, please contact your local Merck office or dealer. Contact Technical Service
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material
cap (push fit)
conical bottom
polypropylene
polypropylene cap
sterility
non-sterile
feature
DNase free
PCR clean
RCF 20,000 × g
RNase free
graduations
packaging
pkg of 250 ea (5 x 50ea)
manufacturer/tradename
Eppendorf® 022431048
capacity
2.0 mL
diam.
10.5 mm
color
clear
suitability
suitable for PCR
binding type
low binding surface
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General description
Eppendorf LoBind® tubes, snap cap, 2.0 mL, PCR clean, colorless, 250 tubes (5 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 for minimal evaporation rates in tube format
- Rated up to 30,000 x g (25,000 x g for 2.0 mL) centrifugation speed for molecular biology applications
Maximize nucleic acid recovery. Eppendorf LoBind Tubes signifcantly reduce sample-to-surface binding to ensure maximal recovery of DNA and RNA molecules. The ideal solution for sample preparation and long-term storage of your precious nucleic acids
Features and Benefits
Signifcantly reduce sample-to-surface binding to ensure maximal recovery of DNA and RNA molecules
Legal Information
Eppendorf is a registered trademark of Eppendorf AG
Eppendorf LoBind is a registered trademark of Eppendorf AG
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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
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
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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