C25120
CM Sephadex® C-25
Synonym(s):
CM Sephadex®, Carboxymethyl Sephadex®
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About This Item
Recommended Products
form
powder
Quality Level
technique(s)
activity assay: suitable
matrix
cross-linked dextran
bead size
40-125 μm (dry)
pore size
~30,000 Da exclusion limit
operating pH
6-10
pH
2—12
capacity
4.0-5.0 meq/g ion exchange capacity
compatibility
mode of use weak cation exchange chromatography
General description
C25120-100G′s updated product number is GE17-0210-01
Application
Sephadex® C-25 is used in ion exchange chromatography, cation exchange media, protein chromatography, separation media and resins. Sephadex® C-25 has been used to study wasp envenomation and to demonstrate that snake protease inhibitors and neurotoxic homologs originated from a common ancestor.
Legal Information
Sephadex is a registered trademark of Cytiva
replaced by
Product No.
Description
Pricing
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Mononuclear and dinuclear ruthenium(III) and ruthenium(IV) complexes of 1,4-dicyanamido-2,5-dimethylbenzene dianion.
Inorgorganica Chimica Acta, 242(1-2), 63-69 (1996)
International journal of biological macromolecules, 45(4), 432-436 (2009-07-29)
Chitooligosaccharides were prepared through hydrolysis of colloidal chitosan by enzyme source from Aspergillusfumigatus BSF114. Chitosan pentamer (COS5) and chitosan hexamer (COS6) were isolated and purified from COS by the ultra-filtration, nano-filtration, ethanol precipitation and the CM-Sephadex C-25 column. COS5 consisted
Distribution and partial characterization of FMRFamide-like peptides in the horseshoe crab, <I>Limulus polyphemus</I>.
Comparative Biochemistry and Physiology. C, 104(1), 79-85 (1993)
The Journal of biological chemistry, 261(23), 10569-10575 (1986-08-15)
Chymodenin, a hormone-like duodenal peptide which rapidly alters the proportions of secreted pancreatic digestive enzymes to a mixture relatively richer in chymotrypsinogen than that found in basal secretion, has been purified to homogeneity. The starting material was an acidic methanol-soluble
Toxicology in vitro : an international journal published in association with BIBRA, 42, 54-60 (2017-04-11)
Aminochrome has been suggested as a more physiological preclinical model capable of inducing five of the six mechanisms of Parkinson's Disease (PD). Until now, there is no evidence that aminochrome induces glial activation related to neuroinflammation, an important mechanism involved
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