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Sigma-Aldrich

SILuMab Stable Isotope-Labeled Monoclonal Antibody Glycan Standard Mouse IgG2b

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About This Item

Code UNSPSC :
12352202
Nomenclature NACRES :
NA.25
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Forme

aqueous solution

Conditions d'expédition

dry ice

Température de stockage

−20°C

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Cet article
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technique(s)

photometry: suitable

technique(s)

photometry: suitable

technique(s)

photometry: suitable

technique(s)

photometry: suitable

form

solution

form

solution

form

liquid

form

liquid

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

storage temp.

15-25°C

storage temp.

15-25°C

storage temp.

15-25°C

storage temp.

15-25°C

analyte chemical class(es)

total organic carbon (TOC)

analyte chemical class(es)

total organic carbon (TOC)

analyte chemical class(es)

-

analyte chemical class(es)

-

pH

4-6 (20 °C in H2O)

pH

4-6 (20 °C in H2O)

pH

4.7 ( in H2O)

pH

4.7 ( in H2O)

Application

Package size based on protein content determined by A280 using an extinction coefficient (E0.1%) of 1.4
SILuMab G is ideal for the qualitative and quantitative analysis of glycoprotein glycans, and can be applied to individual glycans or complex mixtures.

Propriétés physiques

SILuMab G is produced by a proprietary process to yield 15N-labeled N-glycans.
Supplied as a frozen solution in phosphate-buffered saline pH 7.5

Informations légales

This product is licensed under U.S. Patent No. 7,396,688 and foreign counterparts from E. I. du Pont de Nemours and Company. The purchase of this product conveys to the buyer the nontransferable right to use the purchased amount of the product for research and development only, including services for a third party for consideration. The buyer cannot sell or otherwise transfer this product, its components or materials made using this product or its components to a third party. Information about licenses for excluded uses is available from: E. I. du Pont de Nemours and Company; Attn: Associate Director, Commercial Development; DuPont Experimental Station E268; 200 Powdermill Rd.; Wilmington, DE 19803; 1-877-881-9787 (voice), 1-302-695-1437 (fax), licensing@dupont.com.
SILu is a trademark of Sigma-Aldrich Co. LLC

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

nwg

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


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Carolyn C Woodroofe et al.
Chembiochem : a European journal of chemical biology, 21(4), 508-516 (2019-08-01)
The reversible oxidation of methionine residues in proteins has emerged as a biologically important post-translational modification. However, detection and quantitation of methionine sulfoxide in proteins is difficult. Our aim is to develop a method for specifically derivatizing methionine sulfoxide residues.
Dennis Kubiczek et al.
Macromolecular bioscience, 20(4), e2000005-e2000005 (2020-02-28)
The pathogenic yeast Candida auris has received increasing attention due to its ability to cause fatal infections, its resistance toward important fungicides, and its ability to persist on surfaces including medical devices in hospitals. To brace health care systems for
Marcus Pickhardt et al.
Current Alzheimer research, 14(7), 742-752 (2017-02-06)
Anti-aggregation drugs play an important role in therapeutic approaches for Alzheimer's disease. We have previously developed a number of compounds that are able to inhibit the pathological aggregation of Tau protein. One common obstacle to application is the limited penetration
Gizella Csire et al.
Journal of inorganic biochemistry, 170, 195-201 (2017-03-07)
The prion protein (PrP) is a membrane-anchored cell surface glycoprotein containing 231 amino acids. It has been associated with a group of neurodegenerative disorders. Copper(II) interaction with the Human Prion 103-112 fragment and its mutants has been studied with various
Zdenek Kukacka et al.
ChemMedChem, 13(9), 909-915 (2018-02-24)
α-Galactosidase (αGal) is a lysosomal enzyme that hydrolyses the terminal α-galactosyl moiety from glycosphingolipids. Mutations in the encoding genes for αGal lead to defective or misfolded enzyme, which results in substrate accumulation and subsequent organ dysfunction. The metabolic disease caused

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