SLHV004SL
Millex™ PVDF syringe filter
Synonym(s):
0.45 μm PVDF syringe filter, Durapore® PVDF syringe filter, Millex-HV 0.45µm Filter Unit, Millex-HV Filter Unit, Millex-HV syringe filter, disposable syringe filter, sterile syringe filter, syringe filter
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About This Item
UNSPSC Code:
41104922
eCl@ss:
32031690
NACRES:
NB.22
Quality Level
General description
Millex™ PVDF syringe filter utilizes PVDF membrane of pore size 0.45 μm and high-density polyethylene housing.
Application
Millex™ PVDF syringe filter is intended for sterile filtration of tissue culture media, additives, buffers, biological solutions.
Features and Benefits
Designed to ensure lowest binding for protein rich solutions.
Legal Information
Durapore is a registered trademark of Merck KGaA, Darmstadt, Germany
Luer-Lok is a registered trademark of Becton-Dickinson & Co.
Millex is a trademark of Merck KGaA, Darmstadt, Germany
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Removal of residual colonic ciprofloxacin in the rat by activated charcoal entrapped within zinc-pectinate beads.
Khoder, Mouhamad, et al.
European Journal of Pharmaceutical Sciences, 41, 281-288 (2010)
The performance of PEGylated nanocapsules of perfluorooctyl bromide as an ultrasound contrast agent.
Raquel Díaz-López et al.
Biomaterials, 31(7), 1723-1731 (2009-12-02)
The surface of polymeric nanocapsules used as ultrasound contrast agents (UCAs) was modified with PEGylated phospholipids in order to escape recognition and clearance by the mononuclear phagocyte system and achieve passive tumor targeting. Nanocapsules consisted of a shell of poly(lactide-co-glycolide)
Holly Brunton et al.
Cell reports, 31(6), 107625-107625 (2020-05-14)
Pancreatic ductal adenocarcinoma (PDAC) can be divided into transcriptomic subtypes with two broad lineages referred to as classical (pancreatic) and squamous. We find that these two subtypes are driven by distinct metabolic phenotypes. Loss of genes that drive endodermal lineage
Articles
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