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technique(s)
affinity chromatography: suitable
matrix active group
phase
application(s)
life science and biopharma
compatibility
Cytiva
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Application
Sephadex® G-15 has been used in the total antioxidant status (TAS) assay. It has also been used to desalt fractions of sea cucumber Holothuria hilla to isolate polysaccharides.
Sephadex® G-15 is a gel filtration medium used in affinity chromatography, protein chromatrography and gel filtration chromatography.
Fractionation Range (MW)
Globular Proteins: <1500
Dextrans: <1500
Fractionation Range (MW)
Globular Proteins: <1500
Dextrans: <1500
Other Notes
G15120-100G′s updated product number is GE17-0020-01
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)
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Analysis of N(?) -Ethyllysine in Human Plasma Proteins by Gas Chromatography-Negative Ion Chemical Ionization/Mass Spectrometry as a Biomarker for Exposure to Acetaldehyde and Alcohol.
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Alcoholism, Clinical and Experimental Research (2012)
L Ramió-Lluch et al.
Animal reproduction science, 115(1-4), 189-200 (2009-01-23)
This study was performed to test the effects of filtration through several chromatographic resins on the semen quality parameters (percentages of viability, altered acrosomes and morphological abnormalities, motion characteristics and the response to the Osmotic Resistance Test) of boar ejaculates
Juan Bruzzo et al.
Journal of cancer research and clinical oncology, 136(10), 1605-1615 (2010-08-12)
The phenomenon of hormesis is characterized by a biphasic dose-response, exhibiting opposite effects in the low- and high-dose zones. In this study, we explored the possibility that the hormesis concept may describe the interactions between two tumors implanted in a
Sanjiv K Mishra et al.
Protein expression and purification, 80(2), 234-238 (2011-07-13)
C-phycoerythrin was isolated and purified from marine Pseudanabaena sp. using two step chromatographic methods. Phycobiliproteins in the marine Pseudanabaena was extracted in 100 mM phosphate buffer (pH 7.2) and precipitated by salting out. The precipitated C-phycoerythrin was purified by gel
Dae-Young Lee et al.
Journal of medicinal food, 15(4), 399-405 (2012-02-10)
Grains of sugary rice were extracted with 80% aqueous methanol, and the concentrated extracts were successively partitioned using ethyl acetate, n-butanol, and water. From the n-butanol fractions, four flavonoid glycosides were isolated through repeated silica gel, octadecyl silica gel, and
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