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6-Fluoro-L-tryptophan
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6-Fluoro-L-tryptophan
Lieferant:
BACHEM BIOCHEMICA
Beschreibung:
N(α)-Fmoc-L-tryptophan
Artikel-Nr:
(MOLEM25104502)
Lieferant:
Molekula
Hersteller-Artikelnummer::
M25104502
Lokale Artikelnummer::
MOLEM25104502
Beschreibung:
N(α)-Boc-L-tryptophan
VE:
1 * 25 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(BACE4000240.0100)
Lieferant:
BACHEM BIOCHEMICA
Hersteller-Artikelnummer::
4000240.0100
Lokale Artikelnummer::
BACE4000240.0100
Beschreibung:
N(α)-Boc-L-tryptophan
VE:
1 * 100 g
This is a MarketSource item. Additional charges may apply
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:
(J64630.MA)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
J64630.MA
Lokale Artikelnummer::
ALFAJ64630.MA
Beschreibung:
A cell-permeable, specific DNA methyltransferases inhibitor.
VE:
1 * 10 mg
Artikel-Nr:
(BOSSBS-12933R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12933R-A647
Lokale Artikelnummer::
BOSSBS-12933R-A647
Beschreibung:
Chymotrypsins are digestive enzymes that can perform proteolysis by cleaving peptides at the carboxyl side of tyrosine, tryptophan, leucine and phenylalanine, although over time they can also hydrolyze other amide bonds, especially those with leucine-donated carboxyls. Chymotrypsins cleave peptide bonds by attacking the non-reactive carbonyl group with a powerful nucleophile, which momentarily becomes covalently bonded to the substrate to form an intermediate. Chymotrypsin B (CTRB1) and Chymotrypsin B2 (CTRB2) are synthesized in the pancreas by protein biosynthesis as precursors that are enzymatically inactive, but become active as three polypeptide molecules that are interconnected by disulfide bonds.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12933R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12933R-A555
Lokale Artikelnummer::
BOSSBS-12933R-A555
Beschreibung:
Chymotrypsins are digestive enzymes that can perform proteolysis by cleaving peptides at the carboxyl side of tyrosine, tryptophan, leucine and phenylalanine, although over time they can also hydrolyze other amide bonds, especially those with leucine-donated carboxyls. Chymotrypsins cleave peptide bonds by attacking the non-reactive carbonyl group with a powerful nucleophile, which momentarily becomes covalently bonded to the substrate to form an intermediate. Chymotrypsin B (CTRB1) and Chymotrypsin B2 (CTRB2) are synthesized in the pancreas by protein biosynthesis as precursors that are enzymatically inactive, but become active as three polypeptide molecules that are interconnected by disulfide bonds.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12933R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12933R-A350
Lokale Artikelnummer::
BOSSBS-12933R-A350
Beschreibung:
Chymotrypsins are digestive enzymes that can perform proteolysis by cleaving peptides at the carboxyl side of tyrosine, tryptophan, leucine and phenylalanine, although over time they can also hydrolyze other amide bonds, especially those with leucine-donated carboxyls. Chymotrypsins cleave peptide bonds by attacking the non-reactive carbonyl group with a powerful nucleophile, which momentarily becomes covalently bonded to the substrate to form an intermediate. Chymotrypsin B (CTRB1) and Chymotrypsin B2 (CTRB2) are synthesized in the pancreas by protein biosynthesis as precursors that are enzymatically inactive, but become active as three polypeptide molecules that are interconnected by disulfide bonds.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12933R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12933R-A488
Lokale Artikelnummer::
BOSSBS-12933R-A488
Beschreibung:
Chymotrypsins are digestive enzymes that can perform proteolysis by cleaving peptides at the carboxyl side of tyrosine, tryptophan, leucine and phenylalanine, although over time they can also hydrolyze other amide bonds, especially those with leucine-donated carboxyls. Chymotrypsins cleave peptide bonds by attacking the non-reactive carbonyl group with a powerful nucleophile, which momentarily becomes covalently bonded to the substrate to form an intermediate. Chymotrypsin B (CTRB1) and Chymotrypsin B2 (CTRB2) are synthesized in the pancreas by protein biosynthesis as precursors that are enzymatically inactive, but become active as three polypeptide molecules that are interconnected by disulfide bonds.
VE:
1 * 100 µl
Lieferant:
BACHEM BIOCHEMICA
Beschreibung:
N-[(Benzyloxy)carbonyl]-L-tryptophan
Artikel-Nr:
(BOSSBS-13312R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13312R-CY5
Lokale Artikelnummer::
BOSSBS-13312R-CY5
Beschreibung:
GCDH is a 438 amino acid protein that localizes to the mitochondrial matrix and belongs to the acyl-CoA dehydrogenase family. Existing as a homotetramer, GCDH uses FAD as a cofactor to catalyze the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine and L-tryptophan metabolism. While GCDH exists as both a long and short isoform, only the long isoform is a functionally active protein. Defects in the gene encoding GCDH are the cause of glutaric acidemia type I (GA-I), an autosomal recessive disorder that is characterized by the accumulation of glutaconic acid and is associated with such symptoms as progressive dystonia and athetosis due to gliosis and neuronal loss in the basal ganglia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13312R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13312R-A680
Lokale Artikelnummer::
BOSSBS-13312R-A680
Beschreibung:
GCDH is a 438 amino acid protein that localizes to the mitochondrial matrix and belongs to the acyl-CoA dehydrogenase family. Existing as a homotetramer, GCDH uses FAD as a cofactor to catalyze the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine and L-tryptophan metabolism. While GCDH exists as both a long and short isoform, only the long isoform is a functionally active protein. Defects in the gene encoding GCDH are the cause of glutaric acidemia type I (GA-I), an autosomal recessive disorder that is characterized by the accumulation of glutaconic acid and is associated with such symptoms as progressive dystonia and athetosis due to gliosis and neuronal loss in the basal ganglia.
VE:
1 * 100 µl
Artikel-Nr:
(04-13-0001-25)
Lieferant:
Novabiochem (Part of Merck)
Hersteller-Artikelnummer::
8.53086.0025
Lokale Artikelnummer::
NOVA8.53086.0025
Beschreibung:
N(α)-Boc-D-tryptophan
VE:
1 * 25 g
Artikel-Nr:
(MOLE20706773-25G)
Lieferant:
Molekula
Hersteller-Artikelnummer::
20706773-25G
Lokale Artikelnummer::
MOLE20706773-25G
Beschreibung:
N-[(Benzyloxy)carbonyl]-L-tryptophan
VE:
1 * 25 g
This is a MarketSource item. Additional charges may apply
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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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