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EP951033308

Eppendorf® Deepwell plates, Protein LoBind, 96 wells

white plate, conical bottom, colorless wells, capacity 500 μL, pkg of 80 ea (10 bags × 8 plates)

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About This Item

UNSPSC Code:
41106300
Material:
clear wells, colorless wells, conical bottom, polypropylene , white plate
Size:
96 wells
Sterility:
non-sterile
Binding type:
low binding surface
Feature:
lid: no
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size

96 wells

binding type

low binding surface

material

clear wells, colorless wells, conical bottom, polypropylene , white plate

sterility

non-sterile

feature

lid: no

packaging

pkg of 80 ea (10 bags × 8 plates)

manufacturer/tradename

Eppendorf® 951033308

capacity

500 μL

well volume

1000 μL

color

white border

suitability

suitable for (protein analysis), suitable for PCR

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General description

Deepwell Plate 96/1000 µL, Protein LoBind], wells colorless, 1,000 µL, PCR clean, white, 80 plates (10 bags × 8 plates)
  • Eppendorf LoBind material ensures excellent 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
  • Unique OptiTrack® matrix: 30 % faster sample identification and fewer pipetting errors
  • RecoverMax well design: optimized well geometry for minimal remaining/dead volume and excellent mixing properties
  • Raised well rims and a smooth surface ensure reliable sealing in plates

Features and Benefits

  • 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
  • High-contrast Unique OptiTrack® matrix: up to 30 % faster sample identification and fewer pipetting errors
  • RecoverMax® well design: optimized well geometry for minimal remaining/dead volume and excellent mixing properties
  • Raised well rims and a smooth surface ensure reliable sealing

Legal Information

Eppendorf is a registered trademark of Eppendorf SE
OptiTrack is a registered trademark of Eppendorf SE
RecoverMax is a registered trademark of Eppendorf SE

Regulatory Information

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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
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
Graziano Colombo et al.
Free radical biology & medicine, 52(9), 1584-1596 (2012-03-06)
Cigarette smoke, a complex mixture of over 7000 chemicals, contains many components capable of eliciting oxidative stress, which may induce smoking-related disorders, including oral cavity diseases. In this study, we investigated the effects of whole (mainstream) cigarette smoke on human
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
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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