EP022431064
Eppendorf® Protein LoBind tubes
capacity 0.5 mL, PCR clean, pkg of 100 ea (2 x 50ea)
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About This Item
UNSPSC Code:
41121703
Recommended Products
material
(push fit)
polypropylene cap
sterility
non-sterile
feature
PCR clean
packaging
pkg of 100 ea (2 x 50ea)
manufacturer/tradename
Eppendorf® 022431064
parameter
-18,000 × g max. RCF
capacity
0.5 mL
diam.
7.3 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, 0.5 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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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
Byung-Gyu Kim et al.
Proteomics, 6(4), 1166-1174 (2006-01-20)
Runx2 is a key transcription factor in osteoblast differentiation, and its activity is regulated by fibroblast growth factors (FGFs). Craniosynostosis, characterized by premature suture closure, results from mutations that generate constitutively active FGF receptors (FGFRs). We previously showed that FGF/FGFR-activated
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
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
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
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