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Merck

916609

Sigma-Aldrich

NanoFabTx device accessory

end fittings for 1.6 mm tubings

別名:

Microfluidic kit, NanoFabTx, Nanoformulation

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About This Item

UNSPSCコード:
41121800
NACRES:
NA.25

詳細

Microfludic hardware kit component
End fittings for 1.6mm tubings x 1

品質水準

アプリケーション

advanced drug delivery

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詳細

NanoFabTx device accessory, end fittings for 1.6 mm tubing is a component of our NanoFabTx microfluidic device kits (911593, 911860, 911879). The kits additionally include a protocol, manifold, tubing, and additional accessories for microfluidic-based synthesis.

アプリケーション

NanoFabTx device accessory, end fittings for 1.6 mm tubing enable the fast and easy connection of 1.6 mm tubing to the microfluidic chip manifold. NanoFabTx device accessory, end fittings for 1.6 mm tubing can be used as a replacement for the component in our NanoFabTx microfluidic device kits (911593, 911860, 911879).

法的情報

NANOFABTX is a trademark of Sigma-Aldrich Co. LLC

試験成績書(COA)

製品のロット番号・バッチ番号を入力して、試験成績書(COA) を検索できます。ロット番号・バッチ番号は、製品ラベルに「Lot」または「Batch」に続いて記載されています。

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文書ライブラリにアクセスする

Andrew Gdowski et al.
Journal of nanobiotechnology, 16(1), 12-12 (2018-02-13)
The process of optimization and fabrication of nanoparticle synthesis for preclinical studies can be challenging and time consuming. Traditional small scale laboratory synthesis techniques suffer from batch to batch variability. Additionally, the parameters used in the original formulation must be
Samar Damiati et al.
Genes, 9(2) (2018-02-22)
Microfluidic devices present unique advantages for the development of efficient drug carrier particles, cell-free protein synthesis systems, and rapid techniques for direct drug screening. Compared to bulk methods, by efficiently controlling the geometries of the fabricated chip and the flow
Xuanyu Li et al.
Advanced drug delivery reviews, 128, 101-114 (2017-12-27)
Microfluidic chips allow the rapid production of a library of nanoparticles (NPs) with distinct properties by changing the precursors and the flow rates, significantly decreasing the time for screening optimal formulation as carriers for drug delivery compared to conventional methods.

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