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EP951032000

Eppendorf® Deepwell plates, DNA LoBind, 96 wells

white plate, conical bottom, colorless wells, capacity 500 μL, pkg of 40 ea (5 bags × 8 plates)

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About This Item

UNSPSC Code:
41106300

material

clear wells
colorless wells
conical bottom
polypropylene
white plate

sterility

non-sterile

feature

lid: no

packaging

pkg of 40 ea (5 bags × 8 plates)

manufacturer/tradename

Eppendorf® 951032000

capacity

500 μL

well volume

500 μL

color

white border

suitability

suitable for PCR
suitable for molecular biology

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General description

Deepwell Plate 96/500µL, DNA LoBind, wells clear, 500 µL, LoBind, PCR clean, white, 40 plates (5 bags × 8 plates)
  • 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

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 AG
OptiTrack is a registered trademark of Eppendorf AG
RecoverMax 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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