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EP022431081

Eppendorf® Protein LoBind tubes

capacity 1.5 mL, PCR clean, pkg of 100 ea (2 x 50ea)

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About This Item

UNSPSC Code:
41121703

material

(push fit)
polypropylene cap

sterility

non-sterile

feature

PCR clean

packaging

pkg of 100 ea (2 x 50ea)

manufacturer/tradename

Eppendorf® 022431081

parameter

-18,000 × g max. RCF

capacity

1.5 mL

diam.

10.7 mm

color

clear

suitability

suitable for PCR

binding type

low binding surface

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General description

Avoid sample loss due to binding to the vessel wall with the Eppendorf Protein LoBind Tubes. A unique two-component polymer mix that creates a hydrophilic surface significantly improves the protein recovery rate and subsequent analyses. With standard reaction vessels, over 90% of the sample can be lost within 24 hours due to binding to the plastic surface. Use Eppendorf LoBind Tubes and you no longer have to worry about losing your valuable samples. Use Eppendorf LoBind Tubes and you no longer have to worry about losing your valuable samples! Eppendorf Protein LoBind products are available in a variety of formats including vials, microwell and deepwell plates to meet the needs of your specific application. Whether you are looking to scale down sample volumes or increase throughput, the LoBind range can help.
Protein LoBind Tubes, snap cap, Protein LoBind, 1.5 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

  • Protein LoBind products are available in a variety of formats including vials, microassay and deepwell plates to meet the needs of your specific application.
  • LoBind range will support scale down sample volumes or increase throughput,
  • Excellent protein recovery - Recover more than 90% of your protein compared to standard vessels
  • Eppendorf Protein LoBind Tubes also offer a significantly higher recovery rate after 96 hours of incubation compared to tubes with low sample binding from other manufacturers.
  • Helps to increase signal intensity in MALDI-TOF analyses, allowing you to detect and analyze even at concentrations normally considered undetectable (1 pmol) compared to standard tubes.

Legal Information

Eppendorf is a registered trademark of Eppendorf AG

Regulatory Information

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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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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
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
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

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