Wyszukano: Aldehyd+laurynowy

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

Wyprzedaż

Numer katalogowy: (BOSSBS-5133R)

Producent: Bioss

Opis: ALDH1B1 belongs to the aldehyde dehydrogenases family of proteins. Aldehyde dehydrogenase is the second enzyme of the major oxidative pathway of alcohol metabolism. The ALDH1B1 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 * 100 µl

Wyprzedaż

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

Wyprzedaż

Producent: Thermo Fisher Scientific

Opis: 4-Chlorobenzaldehyd ≥98%

MSDS Certyfikaty

Producent: Thermo Fisher Scientific

Opis: 4-Fluorobenzaldehyd ≥98%

MSDS Certyfikaty

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

Wyprzedaż

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

Wyprzedaż

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

Wyprzedaż

Producent: Apollo Scientific

Opis: 2,3,4-Trimetoksybenzaldehyd 97%

Producent: Apollo Scientific

Opis: 2,4,5-Trifluorobenzaldehyd 98%

Producent: Apollo Scientific

Opis: 3,5-Dimetoksybenzaldehyd 97%

Producent: Thermo Fisher Scientific

Opis: 1,1-Dimetoksyaceton 98%

MSDS

Producent: Thermo Fisher Scientific

Opis: 3,4,5-Trimetoksybenzaldehyd 99%

MSDS

Producent: Apollo Scientific

Opis: 2-Bromobenzaldehyd

Producent: Apollo Scientific

Opis: 3,4-Dimetylobenzaldehyd

Producent: Apollo Scientific

Opis: 3,5-Difluorobenzaldehyd 98%