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A8530
m-Aminophenylboronsäure–Agarose
saline suspension
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5 ML
CHF 163.00
CHF 163.00
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Größe auswählen
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5 ML
CHF 163.00
About This Item
CHF 163.00
Check Cart for Availability
Empfohlene Produkte
Form
saline suspension
Qualitätsniveau
Kennzeichnungsgrad
5-20 μmol per mL
Matrix
cross-linked 6% beaded agarose
Matrixaktivierung
epoxy
Matrixanbindung
amino
Matrix-Spacer
12 atoms
Lagertemp.
2-8°C
SMILES String
[X]Nc1cc(ccc1)B(O)O
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Allgemeine Beschreibung
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.[1]
Anwendung
Physikalische Form
Suspension in 0.5 M NaCl, 0.1 M sodium acetate, pH 5.0.
Lagerklassenschlüssel
10 - Combustible liquids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
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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
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
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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