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Merck

EP022431102

Eppendorf® LoBind 蛋白质离心管

capacity 2.0 mL, PCR clean, pkg of 100 ea (2 x 50ea)

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About This Item

分類程式碼代碼:
41121703

材料

(push fit)
polypropylene cap

無菌

non-sterile

特點

PCR clean

包裝

pkg of 100 ea (2 x 50ea)

製造商/商標名

Eppendorf® 022431102

參數

-18,000 × g max. RCF

容量

2.0 mL

直徑

10.5 mm

顏色

clear

適合性

suitable for PCR

結合類型

low binding surface

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一般說明

Protein LoBind Tubes, snap cap, Protein LoBind, 2.0 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

特點和優勢

Eppendorf Protein LoBind Tubes are specifically designed to ensure you get maximal protein recovery.

法律資訊

Eppendorf is a registered trademark of Eppendorf AG

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Rebecca F Turcotte et al.
Biochemical and biophysical research communications, 377(2), 512-514 (2008-10-22)
One of the tightest known protein-protein interactions in biology is that between members of the ribonuclease A superfamily and the ribonuclease inhibitor protein (RI). Some members of this superfamily are able to kill cancer cells, and the ability to evade
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
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
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
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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