UFC30HV
Ultrafree® Centrifugal Filter, 0.5 mL Sample Volume
pore size 0.45 μm, PVDF membrane (hydrophilic)
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Synonym(s):
Centrifuge filter
UNSPSC Code:
41104916
eCl@ss:
36100101
NACRES:
NB.24
Recommended Products
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
Related Categories
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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