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UFC30HV

Millipore

Ultrafree® Centrifugal Filter, 0.5 mL Sample Volume

pore size 0.45 μm, PVDF membrane (hydrophilic)

Synonym(s):

Centrifuge filter

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About This Item

UNSPSC Code:
41104916
eCl@ss:
36100101
NACRES:
NB.24

material

PVDF membrane (hydrophilic)
polypropylene

Quality Level

sterility

non-sterile

feature

holdup volume 5 μL

manufacturer/tradename

Ultrafree®

parameter

0.5 mL sample volume
50 °C max. temp.

technique(s)

protein extraction: suitable
protein purification: suitable

L

45 mm

diam.

10.6 mm

filtration area

0.2 cm2

matrix

Durapore®

pore size

0.45 μm pore size

application(s)

sample preparation

shipped in

ambient

General description

The Ultrafree®-MC centrifugal devices are single-use, disposable filters used for removing particulates from aqueous biological solutions.

Application

Ultrafree®-MC Centrifugal Filter has been used:
  • in co-immunoprecipitation of signaling proteins
  • in indirect labeling for the preparation of fluorescent probes used for microarray hybridization experiments
  • to remove magnetic bead particles from solution in RNA editing method

Legal Information

Durapore is a registered trademark of Merck KGaA, Darmstadt, Germany
Ultrafree is a registered 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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Rémy Bruggmann et al.
Plant molecular biology, 58(2), 247-267 (2005-07-20)
Powdery mildew is an important disease of wheat caused by the obligate biotrophic fungus Blumeria graminis f. sp. tritici. This pathogen invades exclusively epidermal cells after penetrating directly through the cell wall. Because powdery mildew colonizes exclusively epidermal cells, it
Masayuki Sakurai et al.
Methods in molecular biology (Clifton, N.J.), 2181, 113-148 (2020-07-31)
RNA editing of adenosines to inosines contributes to a wide range of biological processes by regulating gene expression post-transcriptionally. To understand the effect, accurate mapping of inosines is necessary. The most conventional method to identify an editing site is to
Javier Garzón et al.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 30(9), 1632-1648 (2005-04-14)
The regulator of G-protein signaling RGS17(Z2) is a member of the RGS-Rz subfamily of GTPase-activating proteins (GAP) that efficiently deactivate GalphazGTP subunits. We have found that in the central nervous system (CNS), the levels of RGSZ2 mRNA and protein are

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