Q0259
Q-Ceramic HyperD® F
50 μm mean particle size
Synonym(s):
HyperD® ceramic ion exchangers
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About This Item
UNSPSC Code:
23201100
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Recommended Products
mean particle size
50 μm
capacity
>0.20 meq/mL
storage temp.
2-8°C
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Application
Ceramic HyperD media are used in protein chromatography and affinity chromatography. Ceramic HyperD media have been used in the development of a capture step of a human recombinant F(ab′)(2) produced and expressed in baculovirus-infected cells and to identify whey proteins as a model system for chromatographic separation of proteins.
Features and Benefits
HyperD media are highly porous, rigid ceramic beads filled with a functionalized hydrophilic gel. The rigid bead allows extremely high linear flow rates without bed compression. The hydrogel exchanges throughout its volume, not just on the surface. And the media do not change volume due to changes in pH or ionic strength.
The supports are stable in commonly used solvents and alkaline or acid environments. Supplied as aqueous suspensions in 1 M NaCl with 20% ethanol to inhibit bacterial growth.
The supports are stable in commonly used solvents and alkaline or acid environments. Supplied as aqueous suspensions in 1 M NaCl with 20% ethanol to inhibit bacterial growth.
Legal Information
HyperD is a registered trademark of Pall Corporation
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Flam. Liq. 3 - Skin Irrit. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
95.0 °F
Flash Point(C)
35 °C
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Svetlana I Novikova et al.
Neurobiology of disease, 23(1), 61-76 (2006-03-22)
This paper describes the high-throughput proteomic analysis of the dorsolateral prefrontal cortex (DLPFC) from schizophrenia (SCHIZ), bipolar (BD), and normal control cohorts from the Harvard Brain Tissue Resource Center performed using ProteinChip technology based on the surface-enhanced laser desorption/ionization time
Olivier Meilhac et al.
Methods in molecular biology (Clifton, N.J.), 357, 331-341 (2006-12-19)
Surface-enhanced laser desorption/ionization time-of-flight mass spectrometry (TOFMS) allows for rapid differential proteomic analysis of various experimental conditions. In the first step of retention chromatography, the proteome to be analyzed is fractionated based on the biochemical properties of the proteins or
John Yee et al.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 27(17), 2787-2792 (2009-05-06)
There are no reliable blood biomarkers to detect early lung cancer. We used a novel strategy that allows discovery of differentially present proteins against a complex and variable background. Mass spectrometry analyses of paired pulmonary venous-radial arterial blood from 16
Cleophas M Kyama et al.
Fertility and sterility, 95(4), 1338-1343 (2010-08-31)
To test the hypothesis that specific proteins and peptides are expressed differentially in eutopic endometrium of women with and without endometriosis and at specific stages of the disease (minimal, mild, moderate, or severe) during the secretory phase. Patients with endometriosis
Kate Gilbert et al.
Methods in molecular biology (Clifton, N.J.), 264, 259-269 (2004-03-17)
Protein-expression profiling of serum is a common approach to the discovery of potential diagnostic and therapeutic markers of disease. Like any other proteome, the serum proteome is characterized by protein expression across a large dynamic range. This single facet requires
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