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4-Methyl-L-tryptophan
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4-Methyl-L-tryptophan
Lieferant:
Novabiochem (Part of Merck)
Beschreibung:
N(α)-Boc-L-tryptophan
Artikel-Nr:
(SIAL15512-5G-F)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
15512-5G-F
Lokale Artikelnummer::
SIAL15512-5G-F
Beschreibung:
N(α)-Boc-L-tryptophan 99,0 TLC_ASSAY_METHOD, Sigma-Aldrich®
VE:
1 * 5 g
Artikel-Nr:
(BACE4003847.0025)
Lieferant:
BACHEM BIOCHEMICA
Hersteller-Artikelnummer::
4003847.0025
Lokale Artikelnummer::
BACE4003847.0025
Beschreibung:
N(α)-Boc-D-tryptophan
VE:
1 * 25 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(BOSSBS-12420R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12420R-A555
Lokale Artikelnummer::
BOSSBS-12420R-A555
Beschreibung:
14-3-3 are activates tyrosine and tryptophan hydroxylases in the presence of Ca (2+)/calmodulin-dependent protein kinase II, and strongly activates protein kinase C. Is probably a multifunctional regulator of the cell signaling processes mediated by both kinases. Activates the ADP-ribosyltransferase (exoS) activity of bacterial origin. 14-3-3 proteins are localized in neurons, and are axonally transported to the nerve terminals. They may be also present, at lower levels, in various other eukaryotic tissues. It belongs to the 14-3-3 family.This antibody is reactive with 14-3-3 Alpha/Beta/Gamma/Delta/Epsilon.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12420R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12420R-CY7
Lokale Artikelnummer::
BOSSBS-12420R-CY7
Beschreibung:
14-3-3 are activates tyrosine and tryptophan hydroxylases in the presence of Ca (2+)/calmodulin-dependent protein kinase II, and strongly activates protein kinase C. Is probably a multifunctional regulator of the cell signaling processes mediated by both kinases. Activates the ADP-ribosyltransferase (exoS) activity of bacterial origin. 14-3-3 proteins are localized in neurons, and are axonally transported to the nerve terminals. They may be also present, at lower levels, in various other eukaryotic tissues. It belongs to the 14-3-3 family.This antibody is reactive with 14-3-3 Alpha/Beta/Gamma/Delta/Epsilon.
VE:
1 * 100 µl
Lieferant:
Alfa Aesar
Beschreibung:
L(-)-Tryptophan Cell Culture
Lieferant:
BACHEM BIOCHEMICA
Beschreibung:
L(-)-Tryptophan
Artikel-Nr:
(BSENM-1616-100)
Lieferant:
Biosensis
Hersteller-Artikelnummer::
M-1616-100
Lokale Artikelnummer::
BSENM-1616-100
Beschreibung:
Tyrosine hydroxylase is an excellent marker for dopaminergic and noradrenergic neurons. Tyrosine hydroxylase (a.k.a. tyrosine 3-monooxygenase) is the enzyme responsible for catalyzing the conversion of the amino acid L-tyrosine to L-3,4-dihydroxyphenylalanine (L-DOPA). L-DOPA is a precursor for dopamine, which, in turn, is a precursor for the important neurotransmitters norepinephrine (noradrenaline) and epinephrine (adrenaline). Tyrosine hydroxylase catalyzes the rate limiting step in this synthesis of catecholamines. In humans, tyrosine hydroxylase is encoded by the TH gene, and the enzyme is present in the central nervous system (CNS), peripheral symphatic neurons and the adrenal medulla. The enzymatic activity of TH requires ferrous ions as cofactors and is believed to be regulated by phosphorylation. At least four isoforms of human TH have been identified which result from alternative splicing. Tyrosine hydroxylase, phenylalanine hydroxylase and tryptophan hydroxylase together make up the family of aromatic amino acid hydroxylases (AAAHs). http://en.wikipedia.org/wiki/Tyrosine_hydroxylase
VE:
1 * 100 µl
Lieferant:
BACHEM BIOCHEMICA
Beschreibung:
N-[(Benzyloxy)carbonyl]-D-tryptophan
Artikel-Nr:
(BOSSBS-9654R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9654R-A750
Lokale Artikelnummer::
BOSSBS-9654R-A750
Beschreibung:
14-3-3 are activates tyrosine and tryptophan hydroxylases in the presence of Ca²⁺/calmodulin-dependent protein kinase II, and strongly activates protein kinase C. Is probably a multifunctional regulator of the cell Signalling processes mediated by both kinases. Activates the ADP-ribosyltransferase (exoS) activity of bacterial origin. 14-3-3 proteins are localised in neurons, and are axonally transported to the nerve terminals. They may be also present, at lower levels, in various other eukaryotic tissues. It belongs to the 14-3-3 family.
VE:
1 * 100 µl
Artikel-Nr:
(BACE4011146.0025)
Lieferant:
BACHEM BIOCHEMICA
Hersteller-Artikelnummer::
4011146.0025
Lokale Artikelnummer::
BACE4011146.0025
Beschreibung:
N-[(Benzyloxy)carbonyl]tryptophan
VE:
1 * 25 g
This is a MarketSource item. Additional charges may apply
Lieferant:
Alfa Aesar
Beschreibung:
N(α)-Acetyl-L-Tryptophan 99
Artikel-Nr:
(BOSSBS-0121R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0121R-A680
Lokale Artikelnummer::
BOSSBS-0121R-A680
Beschreibung:
SYAP1 (synapse-associated protein 1) is a 352 amino acid protein that is ubiquitously expressed in adult tissues. SYAP1 contains one BSD domain which is a novel domain that is present in basal transcription factors, synapse-associated proteins and several hypothetical proteins. The BSD domain is characterised by three predicted alpha helices and by conserved tryptophan and phenylalanine residues, located at the C-terminus of the domain. The gene that encodes SYAP1 in humans is located on chromosome X. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-0121R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0121R-FITC
Lokale Artikelnummer::
BOSSBS-0121R-FITC
Beschreibung:
SYAP1 (synapse-associated protein 1) is a 352 amino acid protein that is ubiquitously expressed in adult tissues. SYAP1 contains one BSD domain which is a novel domain that is present in basal transcription factors, synapse-associated proteins and several hypothetical proteins. The BSD domain is characterized by three predicted alpha helices and by conserved tryptophan and phenylalanine residues, located at the C-terminus of the domain. The gene that encodes SYAP1 in humans is located on chromosome X. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-0121R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0121R-A750
Lokale Artikelnummer::
BOSSBS-0121R-A750
Beschreibung:
SYAP1 (synapse-associated protein 1) is a 352 amino acid protein that is ubiquitously expressed in adult tissues. SYAP1 contains one BSD domain which is a novel domain that is present in basal transcription factors, synapse-associated proteins and several hypothetical proteins. The BSD domain is characterised by three predicted alpha helices and by conserved tryptophan and phenylalanine residues, located at the C-terminus of the domain. The gene that encodes SYAP1 in humans is located on chromosome X. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11784R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11784R-CY5
Lokale Artikelnummer::
BOSSBS-11784R-CY5
Beschreibung:
SPR, also known as sepiapterin reductase, is a homodimeric cytoplasmic protein that belongs to the sepiapterin reductase family. SPR functions as an NADH-dependent aldo-keto reductase and specifically catalyzes the reduction of pteridine derivatives. In addition, SPR plays an important role in tetrahydrobiopterin (BH4) biosynthesis, catalyzing the final reduction step of the synthesis pathway. BH4 is an essential cofactor for the hydroxylation of the aromatic amino acids (tryptophan, tyrosine and phenylalanine) and is required for proper dopamine synthesis. Mutations in the gene encoding SPR can cause sepiapterin reductase deficiency, a monoamine neurotransmitter deficiency without hyperphenylalaninemia. Sepiapterin reductase deficiency interferes with BH4 synthesis, resulting in DOPA-responsive dystonia and a variety of other human diseases. In addition, SPR mRNA expression is increased in the brain of Parkinson’s Disease (PD) patients, suggesting that SPR may play a role in PD.
VE:
1 * 100 µl
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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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