EP951032921
Eppendorf® Deepwell plates, Protein LoBind, 96 wells
yellow plate, conical bottom, colorless wells, capacity 500 μL, pkg of 20 ea (5 bags × 4 plates)
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About This Item
分類程式碼代碼:
41106300
材料:
clear wells
colorless wells
conical bottom
polypropylene
yellow plate
colorless wells
conical bottom
polypropylene
yellow plate
容量:
500 μL
孔容積:
1000 μL
無菌:
non-sterile
結合類型:
low binding surface
特點:
lid: no
推荐产品
材料
clear wells
colorless wells
conical bottom
polypropylene
yellow plate
無菌
non-sterile
特點
lid: no
包裝
pkg of 20 ea (5 bags × 4 plates)
製造商／商標名
Eppendorf® 951032921
容量
500 μL
孔容積
1000 μL
顏色
yellow border
適合性
suitable for (protein analysis)
suitable for PCR
結合類型
low binding surface
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相关类别
一般說明
Deepwell Plate 96/1000 µL, Protein LoBind, wells colorless, 1,000 µL, PCR clean, yellow, 20 plates (5 bags × 4 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
特點和優勢
- 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
法律資訊
Eppendorf is a registered trademark of Eppendorf AG
OptiTrack is a registered trademark of Eppendorf AG
RecoverMax is a registered trademark of Eppendorf AG
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
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
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
Jintang He et al.
Methods in molecular biology (Clifton, N.J.), 1002, 115-122 (2013-04-30)
Glycoproteins play an important role in cell signaling and cell-cell interaction. The alterations of glycoproteins are often relevant to progression of diseases, and these changed glycoproteins can be important biomarkers. The lectin-based glycoproteomic technology has extensively been used for high-throughput
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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