EP022431048
Eppendorf® DNA LoBind tubes
capacity 2.0 mL, PCR clean, pkg of 250 ea (5 x 50ea)
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About This Item
UNSPSC Code:
41103037
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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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Kelly Hodge et al.
Journal of proteomics, 88, 92-103 (2013-03-19)
Mass spectrometry, in the past five years, has increased in speed, accuracy and use. With the ability of the mass spectrometers to identify increasing numbers of proteins the identification of undesirable peptides (those not from the protein sample) has also
Cláudia P Grou et al.
The Journal of biological chemistry, 283(21), 14190-14197 (2008-03-25)
According to current models of peroxisomal biogenesis, newly synthesized peroxisomal matrix proteins are transported into the organelle by Pex5p. Pex5p recognizes these proteins in the cytosol, mediates their membrane translocation, and is exported back into the cytosol in an ATP-dependent
Hongchang Qu et al.
Immunobiology, 218(4), 496-505 (2012-07-17)
Therapeutic modulation of the complement system has become increasingly important in line with the growing recognition of the role of complement in numerous diseases. Compstatin, a peptidic inhibitor that acts at the central level of the complement cascade, is currently
Arzu Umar et al.
Proteomics, 7(2), 323-329 (2006-12-14)
Proteomics assays hold great promise for unraveling molecular events that underlie human diseases. Effective analysis of clinical samples is essential, but this task is considerably complicated by tissue heterogeneity. Laser capture microdissection (LCM) can be used to selectively isolate target
Steven J Bark et al.
Journal of proteome research, 6(11), 4511-4516 (2007-09-14)
Differential recovery of peptides due to nonspecific adsorption can seriously compromise reproducibility and quality of proteomic data for peptide analyses by liquid chromatography-mass spectrometry (LC-MS). This study demonstrates large variations in reproducibility and quantitation of LC-MS data for peptides derived
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