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EP022431102

Eppendorf® Protein LoBind tubes

capacity 2.0 mL, PCR clean, pkg of 100 ea (2 x 50ea)

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About This Item

Code UNSPSC :
41121703
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Matériaux

(push fit)
polypropylene cap

Stérilité

non-sterile

Caractéristiques

PCR clean

Conditionnement

pkg of 100 ea (2 x 50ea)

Fabricant/nom de marque

Eppendorf® 022431102

Paramètres

-18,000 × g max. RCF

Capacité

2.0 mL

Diamètre

10.5 mm

Couleur

clear

Adéquation

suitable for PCR

Type de liaison

low binding surface

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Description générale

Avoid losing valuable samples during centrifugation, incubation and storage! Rely on the excellent protection offered by the hinged Safe-Lock lid. It contains all of our experience from 50 years of continuous optimization and development. Trust the original Eppendorf Safe-Lock Tubes, because your samples deserve only the best.
Protein LoBind Tubes, snap cap, Protein LoBind, 2.0 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

Caractéristiques et avantages

Eppendorf Protein LoBind Tubes are specifically designed to ensure you get maximal protein recovery.

Informations légales

Eppendorf is a registered trademark of Eppendorf AG

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Certificats d'analyse (COA)

Lot/Batch Number

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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
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
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
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
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
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