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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

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

DNA LoBind® Tubes, snap cap, DNA LoBind®, 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 × g for 2,0 mL) centrifugation speed for molecular biology applications

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «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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