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Bis(2-methoxyethyl)amin
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Bis(2-methoxyethyl)amin
Lieferant:
CHEMPUR SILANE
Beschreibung:
Bis(dimethylamino)diethylsilan
Artikel-Nr:
(BOSSBS-7765R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7765R-A488
Lokale Artikelnummer::
BOSSBS-7765R-A488
Beschreibung:
In the process of endocytosis, essential rate-limiting regulator of a fast recycling pathway back to the plasma membrane. During cytokinesis, required for the postfurrowing terminal steps, namely for intercellular bridge stability and abscission, possibly by controlling phosphatidylinositol 4,5-bis phosphate (PIP2) and SEPT2 localization at the intercellular bridge.
VE:
1 * 100 µl
Lieferant:
FLUOROCHEM
Beschreibung:
2-Amino-4-methylpyridin
Artikel-Nr:
(ROCK609-1310)
Lieferant:
Rockland Immunochemicals
Hersteller-Artikelnummer::
609-1310
Lokale Artikelnummer::
ROCK609-1310
Beschreibung:
Anti-human kappa chain Antibody has been assayed against 1.0 µg of human kappa light chain in a standard capture ELISA using ABTS (2,2’-azino-bis-(3-ethylbenthiazoline-6-sulfonic acid)) as a substrate for 30 minutes at room temperature.
VE:
1 * 1 mg
Artikel-Nr:
(PRSI26-030)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
26-030
Lokale Artikelnummer::
PRSI26-030
Beschreibung:
Copper amine oxidases catalyze the oxidative conversion of amines to aldehydes and ammonia in the presence of copper and quinone cofactor. The protein contains several conserved motifs including the active site of amine oxidases and the histidine residues that likely bind copper. It may be a critical modulator of signal transmission in retina, possibly by degrading the biogenic amines dopamine, histamine, and putrescine. Copper amine oxidases catalyze the oxidative conversion of amines to aldehydes and ammonia in the presence of copper and quinone cofactor. This gene shows high sequence similarity to copper amine oxidases from various species ranging from bacteria to mammals. The protein contains several conserved motifs including the active site of amine oxidases and the histidine residues that likely bind copper. It may be a critical modulator of signal transmission in retina, possibly by degrading the biogenic amines dopamine, histamine, and putrescine. This gene may be a candidate gene for hereditary ocular diseases. Alternate splicing results in multiple transcript variants.
VE:
1 * 50 µG
Lieferant:
SIGMA ALDRICH MICROSCOPY
Beschreibung:
Erythrosin extra bluish is a brown color powder, that is soluble in ethanol and water. Its pH ranges from 2,5 to 4. It is used in color filters, light emitting diodes, cosmetics, hair dyes and more. It has several biological applications like detecting gene expression, treating age related macular degeneration, diabetes, obesity and more.
Artikel-Nr:
(MOLE17295435-5G)
Lieferant:
Molekula
Hersteller-Artikelnummer::
17295435-5G
Lokale Artikelnummer::
MOLE17295435-5G
Beschreibung:
8-Aminochinolin
VE:
1 * 5 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(SIAL188778-5G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
188778-5G
Lokale Artikelnummer::
SIAL188778-5G
Beschreibung:
5-Amino-2-chlorpyridin, Sigma-Aldrich®
VE:
1 * 5 g
Artikel-Nr:
(MOLEM18963277)
Lieferant:
Molekula
Hersteller-Artikelnummer::
M18963277
Lokale Artikelnummer::
MOLEM18963277
Beschreibung:
Tryptamin
VE:
1 * 25 g
This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(MAYBSB01321.50)
Lieferant:
Thermo Scientific
Hersteller-Artikelnummer::
SB01321.50
Lokale Artikelnummer::
MAYBSB01321.50
Beschreibung:
4-Aminopyridin
VE:
1 * 50 g
This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(BOSSBS-11797R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11797R-HRP
Lokale Artikelnummer::
BOSSBS-11797R-HRP
Beschreibung:
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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11797R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11797R-A647
Lokale Artikelnummer::
BOSSBS-11797R-A647
Beschreibung:
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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11773R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11773R-A647
Lokale Artikelnummer::
BOSSBS-11773R-A647
Beschreibung:
Terminally differentiating mammalian epidermal cells acquire an insoluble, 10 to 20 nm thick protein deposit on the intracellular surface of the plasma membrane, known as the cross-linked cell envelope (CE). The CE is a component of the epidermis that is generated through the formation of disulfide bonds and gamma-glutamyl-lysine isodipeptide bonds, which are formed by the action of transglutaminases (TGases). TGases are Ca2+-dependent enzymes, which catalyze the formation of isopeptide bonds by transferring an amine to a glutaminyl residue, thereby cross-linking glutamine residues and lysine residues in substrate proteins. TGases influence numerous biological processes, including blood coagulation, epidermal differentiation, seminal fluid coagulation, fertilization, cell differentiation and apoptosis. TGase6 (transglutaminase 6), also known as TGM6, TGY or TGM3L, is a 706 amino acid protein that catalyzes the cross-linking of proteins and the conjugation of proteins to polyamines. As a result of alternative splicing, two TGase6 isoforms exist.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11797R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11797R-A488
Lokale Artikelnummer::
BOSSBS-11797R-A488
Beschreibung:
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.
VE:
1 * 100 µl
Artikel-Nr:
(SIAL193232-10G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
193232-10G
Lokale Artikelnummer::
SIAL193232-10G
Beschreibung:
6-Amino-1,4-benzodioxan, Sigma-Aldrich®
VE:
1 * 10 g
Lieferant:
Novabiochem (Part of Merck)
Beschreibung:
4-(Dimethylamino)pyridin
Preis auf Anfrage
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 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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