Sie suchten nach: N-Fmoc-6-Fluoro-L-tryptophan

Artikel-Nr: (BOSSBS-11489R-HRP)

Lieferant: Bioss

Beschreibung: TNRC6B is a 1,723 amino acid protein that exists as two alternatively spliced isoforms and is thought to be involved in mRNA cleavage events. Expressed ubiquitously, TNRC6B contains one glycine/tryptophan (GW)-rich N-terminal domain, one central glutamine-rich region and one C-terminal RNA recognition motif and is encoded by a gene that maps to human chromosome 22. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein BCR-Abl, a potent cell proliferation activator found in several types of leukemias.

UOM: 1 * 100 µl

Aktion

Artikel-Nr: (BOSSBS-11489R-CY7)

Lieferant: Bioss

Beschreibung: TNRC6B is a 1,723 amino acid protein that exists as two alternatively spliced isoforms and is thought to be involved in mRNA cleavage events. Expressed ubiquitously, TNRC6B contains one glycine/tryptophan (GW)-rich N-terminal domain, one central glutamine-rich region and one C-terminal RNA recognition motif and is encoded by a gene that maps to human chromosome 22. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein BCR-Abl, a potent cell proliferation activator found in several types of leukemias.

UOM: 1 * 100 µl

Aktion

Artikel-Nr: (BOSSBS-0121R-A647)

Lieferant: Bioss

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.

UOM: 1 * 100 µl

Aktion

Lieferant: Thermo Fisher Scientific

Beschreibung: L(-)-Tryptophan 99%

Sicherheitsdatenblätter

Lieferant: Thermo Fisher Scientific

Beschreibung: N(α)-Acetyl-L-Tryptophan ≥99%

Sicherheitsdatenblätter Zertifikate

Lieferant: Merck

Beschreibung: Chromogene Medien bieten ein Verfahren für die schnelle Bestimmung von charakteristischen bakteriellen Enzymen. Merck bietet eine große Auswahl an festen und flüssigen Nährmedien an, die auch die Fluoreszenz-Detektion von E. coli unter dem Markennamen Fluorocult® erlauben. Fluorocult® Nährmedien haben die gleichen Komponenten wie die Standardmedien und zusätzlich das Substrat MUG. Einige der Medien enthalten auch Tryptophan als Substrat für eine mögliche Indolreaktion zur weiteren Bestimmung von E. coli. Mit der Fluorocult® Methode ist ein positives Ergebnis bereits nach 24 bis 48 Stunden möglich. Bei chromogenen Medien ist eine direkte Bestimmung mit der charakteristischen Kolonienfärbung auf dem Nährmedium selbst möglich, ohne die Anwendung von weiteren Zusatzstoffen. Eine Differenzierung von positiven einzelnen Kolonien ist auch möglich, wenn hohe Keimzahlen vorhanden sind.

Sicherheitsdatenblätter Zertifikate

Lieferant: Merck

Beschreibung: N(α)-Acetyl-L-Tryptophan, Sigma-Aldrich®

Artikel-Nr: (BOSSBS-11784R-A750)

Lieferant: Bioss

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 catalyses 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.

UOM: 1 * 100 µl

Aktion

Artikel-Nr: (BOSSBS-11784R-A647)

Lieferant: Bioss

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.

UOM: 1 * 100 µl

Aktion

Lieferant: Merck

Beschreibung: L(-)-Tryptophan, Sigma-Aldrich®

Artikel-Nr: (BOSSBS-11784R-CY5)

Lieferant: Bioss

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.

UOM: 1 * 100 µl

Aktion

Artikel-Nr: (MOLEM52045958)

Lieferant: Molekula

Beschreibung: DL-Tryptophan

UOM: 1 * 25 g

Aktion

 This is a MarketSource item. Additional charges may apply

Lieferant: Thermo Fisher Scientific

Beschreibung: L(-)-Tryptophan Reagenz für die Zellkultur

Sicherheitsdatenblätter Zertifikate

Artikel-Nr: (1.08396.1000)

Lieferant: MERCK PRODUCTION CHEMICALS

Beschreibung: L-Tryptophan, EMPROVE® EXPERT JPC, BP, Ph. Eur., reinst geeignet für die Verwendung als Trägerstoff, SAFC®

UOM: 1 * 1 kg

Sicherheitsdatenblätter Zertifikate Aktion

Artikel-Nr: (MOLEM25104502)

Lieferant: Molekula

Beschreibung: N(α)-Boc-L-tryptophan

UOM: 1 * 25 g

Aktion

 This is a MarketSource item. Additional charges may apply

Artikel-Nr: (BOSSBS-11489R-A350)

Lieferant: Bioss

Beschreibung: TNRC6B is a 1,723 amino acid protein that exists as two alternatively spliced isoforms and is thought to be involved in mRNA cleavage events. Expressed ubiquitously, TNRC6B contains one glycine/tryptophan (GW)-rich N-terminal domain, one central glutamine-rich region and one C-terminal RNA recognition motif and is encoded by a gene that maps to human chromosome 22. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein BCR-Abl, a potent cell proliferation activator found in several types of leukemias.

UOM: 1 * 100 µl

Aktion