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You Searched For: Acetaldehyde+oxime+(mixture+of+syn+and+anti)


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4-(tert-Butyl)cyclohexanone oxime 95%

Supplier: Apollo Scientific
Description: 4-(tert-Butyl)cyclohexanone oxime 95%

Image Unavailable-ANTIA288723-3

Anti-Synaptophysin(Syn) Rabbit Monoclonal Antibody [clone: YN01565r]

Supplier: ANTIBODIES.COM
Description: Anti-Synaptophysin(Syn) Rabbit Monoclonal Antibody [clone: YN01565r]

New Product

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Acetal ≥99%

Supplier: Thermo Fisher Scientific
Description: Acetal ≥99%

MSDS Certificates

Image Unavailable-APOSPC450222-25G

4-(Trifluoromethyl)benzaldehyde oxime

Catalog Number: (APOSPC450222-25G)
Supplier: Apollo Scientific
Description: 4-(Trifluoromethyl)benzaldehyde oxime
UOM: 1 * 25 g
Image Unavailable-BOSSBS-11797R-CY5

Anti-ALDH3A2 Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (BOSSBS-11797R-CY5)
Supplier: 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
Image Unavailable-BOSSBS-11797R-CY7

Anti-ALDH3A2 Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (BOSSBS-11797R-CY7)
Supplier: 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
Image Unavailable-APOSOR26239-1G

Indan-1-one oxime

Catalog Number: (APOSOR26239-1G)
Supplier: Apollo Scientific
Description: Indan-1-one oxime
UOM: 1 * 1 g
Image Unavailable-APOSOR14020-1G

3-Methylpyridine-2-acetamide oxime

Supplier: Apollo Scientific
Description: 3-Methylpyridine-2-acetamide oxime

Image Unavailable-APOSOR913084-1G

3-Methoxyphenylglyoxal hydrate 96%

Supplier: Apollo Scientific
Description: 3-Methoxyphenylglyoxal hydrate 96%

Image Unavailable-1A00510.

Budesonide Acetaldehyde Acetal, Pharmaceutical Analytical Impurities

Catalog Number: (1A00510.)
Supplier: USP
Description: Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.
UOM: 1 * 25 mg
Image Unavailable-APOSOR111254-1G

Imidazo[1,2-a]pyridine-6-carbaldehyde oxime

Catalog Number: (APOSOR111254-1G)
Supplier: Apollo Scientific
Description: Imidazo[1,2-a]pyridine-6-carbaldehyde oxime
UOM: 1 * 1 g
Image Unavailable-APOSOR923437-5G

5-Methyl-2-hexanone oxime 95%

Supplier: Apollo Scientific
Description: 5-Methyl-2-hexanone oxime 95%

Image Unavailable-APOSOR12085-1G

6,7-Dimethyl-1,4-dihydro-2,3-quinoxalinedione2-oxime

Catalog Number: (APOSOR12085-1G)
Supplier: Apollo Scientific
Description: 6,7-Dimethyl-1,4-dihydro-2,3-quinoxalinedione2-oxime
UOM: 1 * 1 g
Image Unavailable-APOSOR110984-1G

4-Bromo-1-methyl-1H-pyrazole-3-carbaldehyde oxime

Catalog Number: (APOSOR110984-1G)
Supplier: Apollo Scientific
Description: 4-Bromo-1-methyl-1H-pyrazole-3-carbaldehyde oxime
UOM: 1 * 1 g
Image Unavailable-BOSSBS-11797R-HRP

Anti-ALDH3A2 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (BOSSBS-11797R-HRP)
Supplier: 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
Image Unavailable-BOSSBS-11797R-A647

Anti-ALDH3A2 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Catalog Number: (BOSSBS-11797R-A647)
Supplier: 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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