SPC50120
SP Sephadex® C-50 sodium form
别名:
Sulfopropyl Sephadex®
bead size
40-125 μm (dry)
pore size
200,000 exclusion limit (av. mol. wt.)
operating pH
2-10
capacity
2.0-2.8 meq/g ion exchange capacity
2.0-2.8 meq/g
compatibility
mode of use strong cation exchange chromatography
Quality Level
Application
SP Sephadex® is used in protein chromatography, ion exchange chromatography and cation exchange media. SP Sephadex® has been used to study human tumors as well as to discuss the biochemical basis for the use of mebendazole in the treatment of echinococcosis.
Legal Information
Sephadex is a registered trademark of Cytiva
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
L Cheng et al.
The Journal of biological chemistry, 266(36), 24404-24412 (1991-12-25)
Rat cellular retinol-binding protein II (CRBP II) is an abundant 134-residue intestinal protein that binds all-trans-retinol and all-trans-retinal. It belongs to a family of homologous, 15-kDa cytoplasmic proteins that bind hydrophobic ligands in a noncovalent fashion. These binding proteins include
J B Starren et al.
Cellular immunology, 104(1), 59-70 (1987-01-01)
We have examined the isotypic pattern of the response of mice to the Ir gene-controlled antigen, dinitrophenyl-ovomucoid (DNP-OM). H-2 kappa mice are high responders (HR); (H-2b,d mice are low responders (LR). The isotype patterns of HR and LR strains differ
R De Prisco et al.
Biochimica et biophysica acta, 788(3), 356-363 (1984-08-14)
A ribonuclease, active on single- and double-stranded RNAs, has been isolated from human seminal plasma 3-5 micrograms of enzyme were recovered per ml of seminal plasma, equivalent to 71% of total activity and a 2500-fold purification (measured with poly(A) X
Isolation and partial characterization of a porcine thyroglobulin-binding <I>Phaseolus vulgaris</I> L. lectin.
Bonorden, W.R., and Swanson, B.G.
Food Chemistry, 44(3), 227-233 (1992)
B G Wallace
The Journal of neuroscience : the official journal of the Society for Neuroscience, 10(11), 3576-3582 (1990-11-01)
Heparin and heparan sulfate have been shown to block nerve-induced acetylcholine-receptor (AChR) aggregation at developing neuromuscular junctions. We found that heparin, heparan sulfate, and a wide variety of other polyanions also inhibited agrin-induced AChR aggregation. The more highly charged the
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