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Description: ALDEHYDE DEHYDROGENASE 10 PROTEIN (HIS-D 1 * 50 µG

Numéro de catalogue: ABCAAB127666-50

UOM: 1 * 50 µG

Fournisseur: Abcam

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Description: ALDEHYDE ASSAY II (COLORIMETRIC - BLUE) 1 * 200 Tests

Numéro de catalogue: ABCAAB219923-200

UOM: 1 * 200 Tests

Fournisseur: Abcam

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Description: ALDEHYDE SITE ASSAY AVIDIN-FITC COMPLEX 1 * 1 Pce

Numéro de catalogue: CAYM600175-1

UOM: 1 * 1 ST

Fournisseur: Cayman Chemical

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Description: ALDEHYDE SITE ASSAY BLOCKING SOLUTION 1 * 10 mL

Numéro de catalogue: CAYM600173-10

UOM: 1 * 10 mL

Fournisseur: Cayman Chemical

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Description: ALDEHYDE QUANTIFICATION ASSAY KIT (FLUOR 1 * 200 Tests

Numéro de catalogue: ABCAAB138882-200

UOM: 1 * 200 Tests

Fournisseur: Abcam

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Description: ALDEHYDE SITE ASSAY BUFFER (10X) 1 * 50 mL

Numéro de catalogue: CAYM600172-50

UOM: 1 * 50 mL

Fournisseur: Cayman Chemical

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Description: Aldh3A2 Antibody: Aldh3A2 is a member of the aldehyde dehydrogenase superfamily, a group of NAD(P)(+)-dependent enzymes that catalyze the oxidation of a wide spectrum of aliphatic and aromatic aldehydes. Aldehyde dehydrogenase enzymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. Aldh3A2 catalyzes the oxidation of long-chain aliphatic aldehydes to fatty acids. Mutations in the Aldh3A2 gene cause Sjogren-Larrson syndrome, an inherited neurocutaneous disorder. Patients with this disorder display ichthyosis, mental retardation and spastic diplegia. The pathogenesis of the cutaneous and neurological symptoms is thought to result from abnormal lipid accumulation in the membranes of skin and brain, the formation of aldehyde Schiff base adducts with amine-containing lipids or proteins, or defective eicosanoid metabolism.

Numéro de catalogue: PRSI4789

UOM: 1 * 1 EA

Fournisseur: ProSci Inc.

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Description: TMR biocytin is a cell-impermeant, fixable fluorescent polar tracer that combines the tetramethylrhodamine (TAMRA) with biotin with an aldehyde-fixable primary amine

Numéro de catalogue: 92003.

UOM: 1 * 5 mg

Fournisseur: Biotium

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Description: 4-Pyridoxic acid is an inactive metabolite of pyridoxine. It is formed from pyridoxine via pyridoxal 5'-phosphate and pyridoxal intermediates by pyridoxine kinase or pyridoxamine phosphate oxidase, as well as pyridoxine-5'-phosphate oxidase, aldehyde dehydrogenase, or aldehyde oxidase.

Numéro de catalogue: CAYM33968-100

UOM: 1 * 100 mg

Fournisseur: Cayman Chemical

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Description: Anti-ALDEHYDE DEHYDROGENASE should be optimized by tthe end user for specific conditions for reactivity.

Numéro de catalogue: ROCK200-4144-0100

UOM: 1 * 1 EA

Fournisseur: Rockland Immunochemicals

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Description: Treatment of the Reformatsky reagent with aldehydes and ketones affords 2,2-difluoro-3-hydroxy esters. Please enquire for references and other data for this item.

Numéro de catalogue: APOSPC3162-500G

UOM: 1 * 500 g

Fournisseur: Apollo Scientific

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Description: Anti-ALDEHYDE DEHYDROGENASE should be optimized by tthe end user for specific conditions for reactivity.

Numéro de catalogue: ROCK200-4144S

UOM: 1 * 25 µl

Fournisseur: Rockland Immunochemicals

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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.

Numéro de catalogue: BOSSBS-11797R-FITC

UOM: 1 * 100 µl

Fournisseur: Bioss

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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.

Numéro de catalogue: BOSSBS-11797R-CY3

UOM: 1 * 100 µl

Fournisseur: Bioss

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Description: ALDH1B1 belongs to the aldehyde dehydrogenases family of proteins. Aldehyde dehydrogenase is the second enzyme of the major oxidative pathway of alcohol metabolism. This gene does not contain introns in the coding sequence. The variation of this locus may affect the development of alcohol-related problems.This protein belongs to the aldehyde dehydrogenases family of proteins. Aldehyde dehydrogenase is the second enzyme of the major oxidative pathway of alcohol metabolism. This gene does not contain introns in the coding sequence. The variation of this locus may affect the development of alcohol-related problems.

Numéro de catalogue: PRSI27-162

UOM: 1 * 50 µG

Fournisseur: ProSci Inc.

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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 catalyses 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 characterised by severe mental retardation, seizures and speech defects. Multiple isoforms of ALDH3A2 exist due to alternative splicing events.

Numéro de catalogue: BOSSBS-11797R-A750

UOM: 1 * 100 µl

Fournisseur: Bioss

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