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Image Unavailable-BOSSBS-11797R-HRP

Anti-ALDH3A2 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Omschrijving: 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.
Catalogus nummer: BOSSBS-11797R-HRP
UOM: 1 * 100 µl
Leverancier: Bioss
Image Unavailable-A17183.14

α-Chloro-p-xylene ≥98%

Omschrijving: α-Chloro-p-xylene ≥98%
Catalogus nummer: A17183.14
UOM: 1 * 25 g
Leverancier: Thermo Fisher Scientific

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Product Image-ACRO328490100

Rottlerin 95+%

Omschrijving: Appearance: Orange to brown Powder
Catalogus nummer: ACRO328490100
UOM: 1 * 10 mg
Leverancier: Thermo Fisher Scientific

MSDS


Image Unavailable-APOSOR40462-25G

α-Bromo-p-xylene 98%

Omschrijving: α-Bromo-p-xylene 98%
Catalogus nummer: APOSOR40462-25G
UOM: 1 * 25 g
Leverancier: Apollo Scientific
Image Unavailable-A13297.22

α-Bromo-p-xylene ≥98%

Omschrijving: α-Bromo-p-xylene ≥98%
Catalogus nummer: A13297.22
UOM: 1 * 100 g
Leverancier: Thermo Fisher Scientific

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Image Unavailable-BOSSBS-11797R-A555

Anti-ALDH3A2 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Omschrijving: 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.
Catalogus nummer: BOSSBS-11797R-A555
UOM: 1 * 100 µl
Leverancier: Bioss
Image Unavailable-BOSSBS-11797R-A680

Anti-ALDH3A2 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Omschrijving: 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.
Catalogus nummer: BOSSBS-11797R-A680
UOM: 1 * 100 µl
Leverancier: Bioss
Image Unavailable-BOSSBS-11797R-A750

Anti-ALDH3A2 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Omschrijving: 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.
Catalogus nummer: BOSSBS-11797R-A750
UOM: 1 * 100 µl
Leverancier: Bioss
Image Unavailable-BOSSBS-12475R-A350

Anti-ANKK1 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Omschrijving: The phosphorylation and dephosphorylation of proteins on serine and threonine residues is an essential means of regulating a broad range of cellular functions in eukaryotes, including cell division, homeostasis and apoptosis. A group of proteins that are intimately involved in this process are the serine/threonine (Ser/Thr) protein kinases. ANKK1 (ankyrin repeat and kinase domain containing 1), also known as PKK2 or SGK288, is a 765 amino acid protein that belongs to the Ser/Thr protein kinase family and contains 12 ANK repeats and one protein kinase domain. Highly expressed in brain tissue and present in lower amounts in placenta and spinal cord, ANKK1 functions to catalyze the ATP-dependent phosphorylation of target proteins and is thought to play a role in alcohol and nicotine dependence. The gene encoding ANKK1 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome.
Catalogus nummer: BOSSBS-12475R-A350
UOM: 1 * 100 µl
Leverancier: Bioss
Image Unavailable-BOSSBS-12475R-CY7

Anti-ANKK1 Rabbit Polyclonal Antibody (Cy7®)

Omschrijving: The phosphorylation and dephosphorylation of proteins on serine and threonine residues is an essential means of regulating a broad range of cellular functions in eukaryotes, including cell division, homeostasis and apoptosis. A group of proteins that are intimately involved in this process are the serine/threonine (Ser/Thr) protein kinases. ANKK1 (ankyrin repeat and kinase domain containing 1), also known as PKK2 or SGK288, is a 765 amino acid protein that belongs to the Ser/Thr protein kinase family and contains 12 ANK repeats and one protein kinase domain. Highly expressed in brain tissue and present in lower amounts in placenta and spinal cord, ANKK1 functions to catalyze the ATP-dependent phosphorylation of target proteins and is thought to play a role in alcohol and nicotine dependence. The gene encoding ANKK1 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome.
Catalogus nummer: BOSSBS-12475R-CY7
UOM: 1 * 100 µl
Leverancier: Bioss
Image Unavailable-ENZOALX350075M010

Rottlerin ≥98% (by HPLC)

Omschrijving: PKCdelta inhibitor
Catalogus nummer: ENZOALX350075M010
UOM: 1 * 10 mg
Leverancier: ENZO LIFE SCIENCES
Image Unavailable-BOSSBS-11797R-CY7

Anti-ALDH3A2 Rabbit Polyclonal Antibody (Cy7®)

Omschrijving: 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.
Catalogus nummer: BOSSBS-11797R-CY7
UOM: 1 * 100 µl
Leverancier: Bioss
Image Unavailable-SPCMD1324-40LBBL

Diisopropanolamine

Omschrijving: Diisopropanolamine, also known as 1-amino-2-propanol or isopropanolamine, is an amino alcohol.
Catalogus nummer: SPCMD1324-40LBBL
UOM: 1 * 40 lb
Leverancier: Spectrum Chemical
Image Unavailable-BOSSBS-11797R-A350

Anti-ALDH3A2 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Omschrijving: 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.
Catalogus nummer: BOSSBS-11797R-A350
UOM: 1 * 100 µl
Leverancier: Bioss
Image Unavailable-J61186.A1

Solvent black 5

Omschrijving: Solvent black 5
Catalogus nummer: J61186.A1
UOM: 1 * 1 kg
Leverancier: Thermo Fisher Scientific

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Image Unavailable-J61281.09

(+/-)-Octopamine hydrochloride 99%

Omschrijving: (+/-)-Octopamine hydrochloride 99%
Catalogus nummer: J61281.09
UOM: 1 * 10 g
Leverancier: Thermo Fisher Scientific

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