C50120
CM Sephadex® C-50
Synonym(s):
CM Sephadex®, Carboxymethyl Sephadex®
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About This Item
Recommended Products
form
powder
technique(s)
activity assay: suitable
bead size
40-125 μm (dry)
pore size
~200,000 Da exclusion limit
operating pH
6-10
capacity
4.0-5.0 meq/g ion exchange capacity
compatibility
mode of use weak cation exchange chromatography
General description
C50120-100G′s updated product number is GE17-0220-01
Application
Sephadex C-50 is used for cation exchange media, separation media, resins, ion exchange chromatography, protein chromatography and affinity chromatography. Sephadex® C-50 has been used to study biochemical characteristics of cobra venom and effects of vitamins on lactoperoxidase enzyme activity.
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
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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Effects of some vitamins on lactoperoxidase enzyme activity.
Sisecioglu, M., et al.
Internat. J. Vit. Nutr. Res., 79, 188-194 (2009)
inetic studies on 1:1 electron-transfer reactions involving blue copper proteins. 15. The reactivity of <I>Anabaena variabilis</I> plastocyanin with inorganic complexes and related NMR studies.
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Journal of the American Chemical Society, 109(21), 6443-6449 (1987)
C Chandra Sekhar et al.
Journal of biosciences, 36(2), 355-361 (2011-06-10)
A fibrinogenolytic toxin of molecular weight 6.5 kDa has been purified from the venom of Indian monocled cobra (Naja kaouthia) by repeated cation exchange chromatography on CM-sephadex C-50. The purified toxin did not show any phospholipase activity but was mildly
Purification and properties of an endoglucanase isolated from the cell walls of <I>Zea mays</I> seedlings.
Hatfield, R., and Nevis, D.J.
Carbohydrate Research, 148(2), 265-278 (1986)
N J Abbott et al.
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Primary culture of rat brain endothelial cells is described, based on the method of C. C. W. Hughes and P. L. Lantos. The cells have been characterised using morphological and immunocytochemical techniques, and systematic studies undertaken to determine the optimal
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