Wyszukano: Aldehyd+maslowy

Numer katalogowy: (ABCAAB219923-200)

Producent: Abcam

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

j.m.: 1 * 200 Tests

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Numer katalogowy: (CAYM600175-1)

Producent: Cayman Chemical

Opis: ALDEHYDE SITE ASSAY AVIDIN-FITC COMPLEX 1 * 1 SZT

j.m.: 1 * 1 SZT

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Numer katalogowy: (CAYM600173-10)

Producent: Cayman Chemical

Opis: ALDEHYDE SITE ASSAY BLOCKING SOLUTION 1 * 10 mL

j.m.: 1 * 10 mL

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Numer katalogowy: (ABCAAB138882-200)

Producent: Abcam

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

j.m.: 1 * 200 Tests

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Numer katalogowy: (CAYM600172-50)

Producent: Cayman Chemical

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

j.m.: 1 * 50 mL

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Numer katalogowy: (ABCAAB257829-1)

Producent: Abcam

Opis: [EN][EN]HUMAN ALDH3A2 ALDEHYDE DEHYDROGE 1 * 1 KIT

j.m.: 1 * 1 KIT

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Numer katalogowy: (92003.)

Producent: Biotium

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

j.m.: 1 * 5 mg

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Producent: Cayman Chemical

Opis: 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.

Numer katalogowy: (ROCK200-4144-0100)

Producent: Rockland Immunochemicals

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

j.m.: 1 * 100 µG

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Numer katalogowy: (1A01560)

Producent: USP

Opis: CHLOROTHIOPHENE ALDEHYDE (25 MG) (5-CHLO 1 * 25 mg

j.m.: 1 * 25 mg

New Product Wyprzedaż

Producent: Apollo Scientific

Opis: 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.

MSDS

Numer katalogowy: (PRSI4789)

Producent: ProSci Inc.

Opis: 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.

j.m.: 1 * 100 µG

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Numer katalogowy: (BOSSBS-11797R-A750)

Producent: Bioss

Opis: 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.

j.m.: 1 * 100 µl

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Numer katalogowy: (BOSSBS-11797R-FITC)

Producent: Bioss

Opis: 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.

j.m.: 1 * 100 µl

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Numer katalogowy: (BOSSBS-11797R-CY3)

Producent: Bioss

Opis: 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.

j.m.: 1 * 100 µl

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Numer katalogowy: (SIAL158127-500G)

Producent: Merck

Opis: Paraformaldehyde is also referred as polyoxymethylene. It participates as an external CO source in the synthesis of aromatic aldehydes and esters.

j.m.: 1 * 500 g

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