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Numer katalogowy: (BOSSBS-11797R-A350)
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


Numer katalogowy: (BOSSBS-11797R-HRP)
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


Numer katalogowy: (BOSSBS-11797R-A647)
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


Numer katalogowy: (BOSSBS-11797R-A488)
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


Numer katalogowy: (BOSSBS-11797R-CY7)
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


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.
Numer katalogowy: (BOSSBS-11797R-CY5)
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


Numer katalogowy: (ROCK200-4144S)
Producent: Rockland Immunochemicals
Opis: Anti-ALDEHYDE DEHYDROGENASE should be optimized by tthe end user for specific conditions for reactivity.
j.m.: 1 * 25 µl


Numer katalogowy: (786-057)
Producent: G-Biosciences
Opis: 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.
j.m.: 1 * 10 mg


Numer katalogowy: (PRSI27-162)
Producent: ProSci Inc.
Opis: 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.
j.m.: 1 * 50 µG


Numer katalogowy: (BOSSBS-4046R-A680)
Producent: Bioss
Opis: 2 Hydroxy phytanoyl CoA lyase catalyses a carbon-carbon cleavage reaction. It cleaves a 2 hydroxy 3 methylacyl CoA into formyl CoA and a 2 methyl branched fatty aldehyde.
j.m.: 1 * 100 µl


Numer katalogowy: (BOSSBS-4046R-HRP)
Producent: Bioss
Opis: 2 Hydroxy phytanoyl CoA lyase catalyzes a carbon-carbon cleavage reaction. It cleaves a 2 hydroxy 3 methylacyl CoA into formyl CoA and a 2 methyl branched fatty aldehyde.
j.m.: 1 * 100 µl


Numer katalogowy: (BOSSBS-4046R-A488)
Producent: Bioss
Opis: 2 Hydroxy phytanoyl CoA lyase catalyzes a carbon-carbon cleavage reaction. It cleaves a 2 hydroxy 3 methylacyl CoA into formyl CoA and a 2 methyl branched fatty aldehyde.
j.m.: 1 * 100 µl


Numer katalogowy: (BOSSBS-4046R-A350)
Producent: Bioss
Opis: 2 Hydroxy phytanoyl CoA lyase catalyzes a carbon-carbon cleavage reaction. It cleaves a 2 hydroxy 3 methylacyl CoA into formyl CoA and a 2 methyl branched fatty aldehyde.
j.m.: 1 * 100 µl


Numer katalogowy: (BOSSBS-4046R-CY7)
Producent: Bioss
Opis: 2 Hydroxy phytanoyl CoA lyase catalyzes a carbon-carbon cleavage reaction. It cleaves a 2 hydroxy 3 methylacyl CoA into formyl CoA and a 2 methyl branched fatty aldehyde.
j.m.: 1 * 100 µl


Numer katalogowy: (BOSSBS-4046R-CY5.5)
Producent: Bioss
Opis: 2 Hydroxy phytanoyl CoA lyase catalyzes a carbon-carbon cleavage reaction. It cleaves a 2 hydroxy 3 methylacyl CoA into formyl CoA and a 2 methyl branched fatty aldehyde.
j.m.: 1 * 100 µl


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