Votre recherche pour: Aldéhyde+propionique

Fournisseur: Thermo Fisher Scientific

Description: Isobutyraldéhyde ≥98%

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Fournisseur: ENZO LIFE SCIENCES

Description: Cell permeable inhibitor of the 26S proteasome (MCP; multicatalytic proteinase complex) in HT4 cells. Causes accumulation of ubiquitinylated proteins in neuronal cells. Prevents the activation of NF-κB in response to TNF-α or okadaic acid through inhibition of IκBα degradation.

Numéro de catalogue: (APOSOR963550-5G)

Fournisseur: Apollo Scientific

Description: Boc-L-alaninal 95%

UOM: 1 * 5 g

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Numéro de catalogue: (786-057)

Fournisseur: G-Biosciences

Description: ALLN is a cell permeable peptide aldehyde inhibitor of calpain I and to a lesser extent calpain II. It also inhibits other neutral cysteine proteases, cathepsin B and L and the proteasome.

UOM: 1 * 10 mg

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Numéro de catalogue: (BOSSBS-11797R-CY5)

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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Numéro de catalogue: (ENZOBMLZW94900100)

Fournisseur: ENZO LIFE SCIENCES

Description: Highly specific aldehyde based inhibitor for the caspase-like peptidic activity of the 20S proteasome.

UOM: 1 * 1 EA

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Numéro de catalogue: (BOSSBS-11797R-CY7)

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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Fournisseur: Thermo Fisher Scientific

Description: 5-Nitrosalicylaldéhyde 98+%

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Fournisseur: Thermo Fisher Scientific

Description: 3-Chlorobenzaldéhyde 99%

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Fournisseur: Thermo Fisher Scientific

Description: Vératraldéhyde 99+%

MSMD

Numéro de catalogue: (ACRO438470010)

Fournisseur: Thermo Fisher Scientific

Description: Boc-L-alaninal 98%

UOM: 1 * 1 g

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Numéro de catalogue: (23438.268)

Fournisseur: VWR Chemicals

Description: 4-(Diméthylamino)benzaldéhyde, TECHNICAL

UOM: 1 * 500 g

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Numéro de catalogue: (BOSSBS-11797R-A350)

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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Fournisseur: Thermo Fisher Scientific

Description: Stabilized with 0.1% hydroquinone

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Fournisseur: Thermo Fisher Scientific

Description: 3-Fluorobenzaldéhyde 98+%

MSMD

Fournisseur: Thermo Fisher Scientific

Description: Phénylacétaldéhyde 98% stabilisé

MSMD