A8530
m-Aminophenylboronic acid–Agarose
saline suspension
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About This Item
Numéro MDL:
Code UNSPSC :
12161501
ID de substance PubChem :
Nomenclature NACRES :
NA.32
Produits recommandés
Forme
saline suspension
Ampleur du marquage
5-20 μmol per mL
Matrice
cross-linked 6% beaded agarose
Activation de la matrice
epoxy
Fixation de matrice
amino
Espaceur de matrice
12 atoms
Température de stockage
2-8°C
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Description générale
m-Aminophenylboronic acid–Agarose is applicable as a boronate affinity matrix for the purification of severe acute respiratory syndrome′s (SARS-CoV) nucleoprotein (NP) antigen.
Application
m-Aminophenylboronic acid–Agarose has been used as a separating gel in the boronate affinity chromatography of albumins. It has also been used as a resin for purification of 3,4-dihydroxyphenylacetaldehyde (DOPAL)-bound α-synuclein (α-syn).
Forme physique
Suspension in 0.5 M NaCl, 0.1 M sodium acetate, pH 5.0.
Code de la classe de stockage
10 - Combustible liquids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
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Philippe Rondeau et al.
Archives of biochemistry and biophysics, 460(1), 141-150 (2007-02-27)
Structural modifications of bovine serum albumin (BSA) induced by heating, and the involvement of glycation of albumin in such processing were studied by using Fourier transform infrared spectroscopy (FTIR) and polyacrylamide gel electrophoresis (PAGE). For native BSA, heating treatments gave
Serge Chesne et al.
Biochimie, 88(10), 1467-1477 (2006-07-04)
Non-enzymatic glycosylation (glycation) and oxidative damages represent major research areas insofar as such modifications of proteins are frequently observed in numerous states of disease. Albumin undergoes structural and functional alterations, caused by increased glycosylation during non insulin-dependent diabetes mellitus, which
Pravin K Bhatnagar et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 863(2), 235-241 (2008-02-09)
Hybrid hybridomas (quadromas) are derived by fusing at least two hybridomas, each producing a different antibody of predefined specificity. The resulting cell secretes not only the immunoglobulins of both parents but also hybrid molecules manifesting the binding characteristics of the
N Plotegher et al.
Scientific reports, 7, 40699-40699 (2017-01-14)
Parkinson's disease is a neurodegenerative disorder characterized by the death of dopaminergic neurons and by accumulation of alpha-synuclein (aS) aggregates in the surviving neurons. The dopamine catabolite 3,4-dihydroxyphenylacetaldehyde (DOPAL) is a highly reactive and toxic molecule that leads to aS
Francesco Longo et al.
Acta neuropathologica communications, 5(1), 22-22 (2017-03-16)
Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene are the most common genetic cause of Parkinson's disease. Here, we investigated whether the G2019S LRRK2 mutation causes morphological and/or functional changes at nigro-striatal dopamine neurons. Density of striatal dopaminergic terminals
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