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Votre recherche pour: Aldéhyde+propionique


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Fournisseur: TCI
Description: 3,4,5-Trihydroxybenzaldéhyde ≥98.0% (par GC, analyse par titration)

Fournisseur: Thermo Fisher Scientific
Description: Isobutyraldéhyde 99+%
Numéro de catalogue: (ABCAAB184171-100)
Fournisseur: Abcam
Description: Anti-Aldehyde dehydrogenase 10 Rabbit Monoclonal Antibody [clone: EPR15425(B)]
UOM: 1 * 100 µl


Fournisseur: Apollo Scientific
Description: Pyruvaldéhyde 40% en solution aqueuse

Fournisseur: Thermo Fisher Scientific
Description: Phénylacétaldéhyde 95%
Numéro de catalogue: (TCIAH1443-25ML)
Fournisseur: TCI
Description: Hexanal diethyl acetal ≥98.0% (par GC)
UOM: 1 * 25 mL


Fournisseur: TCI
Description: 1-Methyl-2-pyrrolecarboxaldehyde ≥97.0% (par GC)

Numéro de catalogue: (BOSSBS-12461R-A750)
Fournisseur: Bioss
Description: Aldehyde dehydrogenases (ALDHs) mediate the NADP+-dependent oxidation of aldehydes into acids and play an important role in the detoxification of alcohol-derived acetaldehyde, as well as in lipid peroxidation and in the metabolism of corticosteroids, biogenic amines and neurotransmitters. ALDH9A1 (aldehyde dehydrogenase family 9 member A1), also known as E3, ALDH4, ALDH7, ALDH9 or TMABADH, is a 494 amino acid cytoplasmic protein that is highly expressed in adult liver, skeletal muscle, kidney and embryonic brain. ALDH9A1 converts gamma-trimethylaminobutyraldehyde into gamma-butyrobetaine and catalyses the irreversible oxidation of a broad range of aldehydes to the corresponding acids in a NAD-dependent reaction.
UOM: 1 * 100 µl


Numéro de catalogue: (BOSSBS-12461R-HRP)
Fournisseur: Bioss
Description: Aldehyde dehydrogenases (ALDHs) mediate the NADP+-dependent oxidation of aldehydes into acids and play an important role in the detoxification of alcohol-derived acetaldehyde, as well as in lipid peroxidation and in the metabolism of corticosteroids, biogenic amines and neurotransmitters. ALDH9A1 (aldehyde dehydrogenase family 9 member A1), also known as E3, ALDH4, ALDH7, ALDH9 or TMABADH, is a 494 amino acid cytoplasmic protein that is highly expressed in adult liver, skeletal muscle, kidney and embryonic brain. ALDH9A1 converts gamma-trimethylaminobutyraldehyde into gamma-butyrobetaine and catalyzes the irreversible oxidation of a broad range of aldehydes to the corresponding acids in a NAD-dependent reaction.
UOM: 1 * 100 µl


Numéro de catalogue: (BOSSBS-12461R-A647)
Fournisseur: Bioss
Description: Aldehyde dehydrogenases (ALDHs) mediate the NADP+-dependent oxidation of aldehydes into acids and play an important role in the detoxification of alcohol-derived acetaldehyde, as well as in lipid peroxidation and in the metabolism of corticosteroids, biogenic amines and neurotransmitters. ALDH9A1 (aldehyde dehydrogenase family 9 member A1), also known as E3, ALDH4, ALDH7, ALDH9 or TMABADH, is a 494 amino acid cytoplasmic protein that is highly expressed in adult liver, skeletal muscle, kidney and embryonic brain. ALDH9A1 converts gamma-trimethylaminobutyraldehyde into gamma-butyrobetaine and catalyzes the irreversible oxidation of a broad range of aldehydes to the corresponding acids in a NAD-dependent reaction.
UOM: 1 * 100 µl


Numéro de catalogue: (BOSSBS-12461R-FITC)
Fournisseur: Bioss
Description: Aldehyde dehydrogenases (ALDHs) mediate the NADP+-dependent oxidation of aldehydes into acids and play an important role in the detoxification of alcohol-derived acetaldehyde, as well as in lipid peroxidation and in the metabolism of corticosteroids, biogenic amines and neurotransmitters. ALDH9A1 (aldehyde dehydrogenase family 9 member A1), also known as E3, ALDH4, ALDH7, ALDH9 or TMABADH, is a 494 amino acid cytoplasmic protein that is highly expressed in adult liver, skeletal muscle, kidney and embryonic brain. ALDH9A1 converts gamma-trimethylaminobutyraldehyde into gamma-butyrobetaine and catalyzes the irreversible oxidation of a broad range of aldehydes to the corresponding acids in a NAD-dependent reaction.
UOM: 1 * 100 µl


Fournisseur: Thermo Fisher Scientific
Description: trans-2-Méthyl-2-butenal 98%
Fournisseur: Apollo Scientific
Description: 5-Nitrosalicylaldéhyde

Numéro de catalogue: (TCIAT1607-5G)
Fournisseur: TCI
Description: 1-(p-Toluenesulphonyl)pyrrole-2-carboxaldehyde ≥98.0% (par analyse titrimétrique)
UOM: 1 * 5 g


Numéro de catalogue: (BOSSBS-11797R-HRP)
Fournisseur: Bioss
Description: Aldehyde dehydrogenases (ALDHs) mediate the NADP+-dependent oxidation of aldehydes into acids and play an important role in the detoxification of alcohol-derived acetaldehyde, as well as in lipid peroxidation and in the metabolism of corticosteroids, biogenic amines and neurotransmitters. ALDH3A2 (aldehyde dehydrogenase 3 family, member A2), also known as SLS, FALDH or ALDH10, is a 485 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the endoplasmic reticulum and belongs to the aldehyde dehydrogenase family. Expressed in a variety of tissues, including liver, heart, lung, brain, kidney and placenta, ALDH3A2 catalyzes the NAD+-dependent oxidation of long-chain aliphatic aldehydes to fatty acids, a process that is necessary for detoxification and lipid metabolism. Defects in the gene encoding ALDH3A2 are the cause of Sjoegren-Larsson syndrome (SLS), an autosomal recessive neurocutaneous disorder characterized by severe mental retardation, seizures and speech defects. Multiple isoforms of ALDH3A2 exist due to alternative splicing events.
UOM: 1 * 100 µl


Numéro de catalogue: (BOSSBS-11797R-A647)
Fournisseur: Bioss
Description: Aldehyde dehydrogenases (ALDHs) mediate the NADP+-dependent oxidation of aldehydes into acids and play an important role in the detoxification of alcohol-derived acetaldehyde, as well as in lipid peroxidation and in the metabolism of corticosteroids, biogenic amines and neurotransmitters. ALDH3A2 (aldehyde dehydrogenase 3 family, member A2), also known as SLS, FALDH or ALDH10, is a 485 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the endoplasmic reticulum and belongs to the aldehyde dehydrogenase family. Expressed in a variety of tissues, including liver, heart, lung, brain, kidney and placenta, ALDH3A2 catalyzes the NAD+-dependent oxidation of long-chain aliphatic aldehydes to fatty acids, a process that is necessary for detoxification and lipid metabolism. Defects in the gene encoding ALDH3A2 are the cause of Sjoegren-Larsson syndrome (SLS), an autosomal recessive neurocutaneous disorder characterized by severe mental retardation, seizures and speech defects. Multiple isoforms of ALDH3A2 exist due to alternative splicing events.
UOM: 1 * 100 µl


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