Sie suchten nach: Methyl-2-hydroxyisobutyrate


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Lieferant: Apollo Scientific
Beschreibung: Methyl-2-hydroxyisobutyrat 95%

Artikel-Nr: (ACRO436180050)
Lieferant: Thermo Scientific
Beschreibung: (R)-(-)-Methyl-3-hydroxyisobutyrat 98%
VE: 1 * 5 g

Lieferant: Thermo Scientific
Beschreibung: Appearance: Clear colorless Liquid
Lieferant: Apollo Scientific
Beschreibung: (R)-(-)-Methyl-3-hydroxyisobutyrat 97%

Lieferant: Thermo Scientific
Beschreibung: (S)-(+)-Methyl-3-hydroxy-2-methylpropionate ≥98%
Lieferant: Merck
Beschreibung: (R)-(-)-Methyl-3-hydroxyisobutyrat, Sigma-Aldrich®

Artikel-Nr: (BOSSBS-15483R-HRP)
Lieferant: Bioss
Beschreibung: HIBADH is a 336 amino acid mitochondrial enzyme that catalyses the NAD+-dependent, reversible oxidisation of 3-Hydroxyisobutyrate to methylmalonate semialdehyde, an intermediate of valine catabolism. The enzyme functions as a homodimer between a pH of 7,0 and 10,0, with optimal activity between 8,8 and 9,0. It was previously hypothesised that defects in the gene encoding HIBADH may be the cause of 3-Hydroxyisobutyric aciduria, a rare disorder that is characterised by a variety of clinical manifestations such as neurodevelopmental problems and dysmorphic features. However, it was shown that HIBADH activity was equal in patients with 3-Hydroxyisobutyric aciduria as compared with controls.
VE: 1 * 100 µl


Lieferant: Thermo Scientific
Beschreibung: Ethyl-2-hydroxyisobutyrat ≥98%
Lieferant: Apollo Scientific
Beschreibung: (R)-3,3,3-Trifluoro-2-hydroxy-2-methylpropionic acid 97%

Artikel-Nr: (BOSSBS-15483R-CY7)
Lieferant: Bioss
Beschreibung: HIBADH is a 336 amino acid mitochondrial enzyme that catalyses the NAD+-dependent, reversible oxidisation of 3-Hydroxyisobutyrate to methylmalonate semialdehyde, an intermediate of valine catabolism. The enzyme functions as a homodimer between a pH of 7,0 and 10,0, with optimal activity between 8,8 and 9,0. It was previously hypothesised that defects in the gene encoding HIBADH may be the cause of 3-Hydroxyisobutyric aciduria, a rare disorder that is characterised by a variety of clinical manifestations such as neurodevelopmental problems and dysmorphic features. However, it was shown that HIBADH activity was equal in patients with 3-Hydroxyisobutyric aciduria as compared with controls.
VE: 1 * 100 µl


Artikel-Nr: (BOSSBS-15483R-A647)
Lieferant: Bioss
Beschreibung: HIBADH is a 336 amino acid mitochondrial enzyme that catalyses the NAD+-dependent, reversible oxidisation of 3-Hydroxyisobutyrate to methylmalonate semialdehyde, an intermediate of valine catabolism. The enzyme functions as a homodimer between a pH of 7,0 and 10,0, with optimal activity between 8,8 and 9,0. It was previously hypothesised that defects in the gene encoding HIBADH may be the cause of 3-Hydroxyisobutyric aciduria, a rare disorder that is characterised by a variety of clinical manifestations such as neurodevelopmental problems and dysmorphic features. However, it was shown that HIBADH activity was equal in patients with 3-Hydroxyisobutyric aciduria as compared with controls.
VE: 1 * 100 µl


Artikel-Nr: (BOSSBS-15483R)
Lieferant: Bioss
Beschreibung: HIBADH is a 336 amino acid mitochondrial enzyme that catalyzes the NAD+-dependent, reversible oxidization of 3-Hydroxyisobutyrate to methylmalonate semialdehyde, an intermediate of valine catabolism. The enzyme functions as a homodimer between a pH of 7.0 and 10.0, with optimal activity between 8.8 and 9.0. It was previously hypothesized that defects in the gene encoding HIBADH may be the cause of 3-Hydroxyisobutyric aciduria, a rare disorder that is characterized by a variety of clinical manifestations such as neurodevelopmental problems and dysmorphic features. However, it was shown that HIBADH activity was equal in patients with 3-Hydroxyisobutyric aciduria as compared with controls.
VE: 1 * 100 µl


Lieferant: Thermo Scientific
Beschreibung: 2-Hydroxyisobuttersäure 98%
Lieferant: Apollo Scientific
Beschreibung: (2S)-3,3,3-Trifluor-2-hydroxy-2-methylpropansäure 95+%

Artikel-Nr: (BOSSBS-15483R-A488)
Lieferant: Bioss
Beschreibung: HIBADH is a 336 amino acid mitochondrial enzyme that catalyses the NAD+-dependent, reversible oxidisation of 3-Hydroxyisobutyrate to methylmalonate semialdehyde, an intermediate of valine catabolism. The enzyme functions as a homodimer between a pH of 7,0 and 10,0, with optimal activity between 8,8 and 9,0. It was previously hypothesised that defects in the gene encoding HIBADH may be the cause of 3-Hydroxyisobutyric aciduria, a rare disorder that is characterised by a variety of clinical manifestations such as neurodevelopmental problems and dysmorphic features. However, it was shown that HIBADH activity was equal in patients with 3-Hydroxyisobutyric aciduria as compared with controls.
VE: 1 * 100 µl


Artikel-Nr: (BOSSBS-15483R-A750)
Lieferant: Bioss
Beschreibung: HIBADH is a 336 amino acid mitochondrial enzyme that catalyses the NAD+-dependent, reversible oxidisation of 3-Hydroxyisobutyrate to methylmalonate semialdehyde, an intermediate of valine catabolism. The enzyme functions as a homodimer between a pH of 7,0 and 10,0, with optimal activity between 8,8 and 9,0. It was previously hypothesised that defects in the gene encoding HIBADH may be the cause of 3-Hydroxyisobutyric aciduria, a rare disorder that is characterised by a variety of clinical manifestations such as neurodevelopmental problems and dysmorphic features. However, it was shown that HIBADH activity was equal in patients with 3-Hydroxyisobutyric aciduria as compared with controls.
VE: 1 * 100 µl


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Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das call noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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