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EP022431048

Eppendorf® DNA LoBind管

capacity 2.0 mL, PCR clean, pkg of 250 ea (5 x 50ea)

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About This Item

分類程式碼代碼:
41103037
暫時無法取得訂價和供貨情況

材料

cap (push fit)
conical bottom
polypropylene
polypropylene cap

無菌

non-sterile

特點

DNase free
PCR clean
RCF 20,000 × g
RNase free
graduations

包裝

pkg of 250 ea (5 x 50ea)

製造商/商標名

Eppendorf® 022431048

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

最大限度回收核酸。 Eppendorf LoBind 管大幅减少样品与表面吸附,确保最大限度回收 DNA 和 RNA 分子。样品制备和长期储存珍贵核酸的理想解决方案
Eppendorf LoBind® tubes, snap cap, 2.0 mL, PCR clean, colorless, 250 tubes (5 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 for minimal evaporation rates in tube format
  • Rated up to 30,000 x g (25,000 x g for 2.0 mL) centrifugation speed for molecular biology applications

特點和優勢

大幅减少样品与表面吸附,确保最大限度回收 DNA 和 RNA 分子

法律資訊

Eppendorf is a registered trademark of Eppendorf AG
Eppendorf LoBind is a registered trademark of Eppendorf AG

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分析證明 (COA)

Lot/Batch Number

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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
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
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
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

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