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Votre recherche pour: Aldéhyde+propionique


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Fournisseur: Thermo Fisher Scientific
Description: Isobutyraldéhyde ≥98%
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


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


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


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


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


Fournisseur: Thermo Fisher Scientific
Description: 5-Nitrosalicylaldéhyde 98+%
Fournisseur: Thermo Fisher Scientific
Description: 3-Chlorobenzaldéhyde 99%
Fournisseur: Thermo Fisher Scientific
Description: Vératraldéhyde 99+%
Numéro de catalogue: (ACRO438470010)
Fournisseur: Thermo Fisher Scientific
Description: Boc-L-alaninal 98%
UOM: 1 * 1 g

MSMD


Numéro de catalogue: (23438.268)
Fournisseur: VWR Chemicals
Description: 4-(Diméthylamino)benzaldéhyde, TECHNICAL
UOM: 1 * 500 g

MSMD Certificats


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


Fournisseur: Thermo Fisher Scientific
Description: Stabilized with 0.1% hydroquinone
Fournisseur: Thermo Fisher Scientific
Description: 3-Fluorobenzaldéhyde 98+%
Fournisseur: Thermo Fisher Scientific
Description: Phénylacétaldéhyde 98% stabilisé
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