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2-[Benzyl(2-hydroxyethyl)amino]-1-ethanol
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2-[Benzyl(2-hydroxyethyl)amino]-1-ethanol
Lieferant:
Sigma-Aldrich
Beschreibung:
Pyrimidin, Sigma-Aldrich®
Artikel-Nr:
(BOSSBS-8287R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8287R-CY3
Lokale Artikelnummer::
BOSSBS-8287R-CY3
Beschreibung:
Catalyzes the second step of the reductive pyrimidine degradation, the reversible hydrolytic ring opening of dihydropyrimidines. Can catalyzes the ring opening of 5,6-dihydrouracil to N-carbamyl-alanine and of 5,6-dihydrothymine to N-carbamyl-amino isobutyrate.Tissue specificity:Liver and kidney.Involvement in disease:Defects in DPYS are the cause of dihydropyrimidinase deficiency (DHPD). DHPD is an autosomal recessive disorder characterized by dihydropyrimidinuria and associated with a variable clinical phenotype: epileptic or convulsive attacks, dysmorphic features and severe developmental delay, and congenital microvillous atrophy.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8287R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8287R-CY5.5
Lokale Artikelnummer::
BOSSBS-8287R-CY5.5
Beschreibung:
Catalyzes the second step of the reductive pyrimidine degradation, the reversible hydrolytic ring opening of dihydropyrimidines. Can catalyzes the ring opening of 5,6-dihydrouracil to N-carbamyl-alanine and of 5,6-dihydrothymine to N-carbamyl-amino isobutyrate.Tissue specificity:Liver and kidney.Involvement in disease:Defects in DPYS are the cause of dihydropyrimidinase deficiency (DHPD). DHPD is an autosomal recessive disorder characterized by dihydropyrimidinuria and associated with a variable clinical phenotype: epileptic or convulsive attacks, dysmorphic features and severe developmental delay, and congenital microvillous atrophy.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8287R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8287R-CY7
Lokale Artikelnummer::
BOSSBS-8287R-CY7
Beschreibung:
Catalyzes the second step of the reductive pyrimidine degradation, the reversible hydrolytic ring opening of dihydropyrimidines. Can catalyzes the ring opening of 5,6-dihydrouracil to N-carbamyl-alanine and of 5,6-dihydrothymine to N-carbamyl-amino isobutyrate.Tissue specificity:Liver and kidney.Involvement in disease:Defects in DPYS are the cause of dihydropyrimidinase deficiency (DHPD). DHPD is an autosomal recessive disorder characterized by dihydropyrimidinuria and associated with a variable clinical phenotype: epileptic or convulsive attacks, dysmorphic features and severe developmental delay, and congenital microvillous atrophy.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8287R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8287R-FITC
Lokale Artikelnummer::
BOSSBS-8287R-FITC
Beschreibung:
Catalyzes the second step of the reductive pyrimidine degradation, the reversible hydrolytic ring opening of dihydropyrimidines. Can catalyzes the ring opening of 5,6-dihydrouracil to N-carbamyl-alanine and of 5,6-dihydrothymine to N-carbamyl-amino isobutyrate.Tissue specificity:Liver and kidney.Involvement in disease:Defects in DPYS are the cause of dihydropyrimidinase deficiency (DHPD). DHPD is an autosomal recessive disorder characterized by dihydropyrimidinuria and associated with a variable clinical phenotype: epileptic or convulsive attacks, dysmorphic features and severe developmental delay, and congenital microvillous atrophy.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8287R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8287R-HRP
Lokale Artikelnummer::
BOSSBS-8287R-HRP
Beschreibung:
Catalyzes the second step of the reductive pyrimidine degradation, the reversible hydrolytic ring opening of dihydropyrimidines. Can catalyzes the ring opening of 5,6-dihydrouracil to N-carbamyl-alanine and of 5,6-dihydrothymine to N-carbamyl-amino isobutyrate.Tissue specificity:Liver and kidney.Involvement in disease:Defects in DPYS are the cause of dihydropyrimidinase deficiency (DHPD). DHPD is an autosomal recessive disorder characterized by dihydropyrimidinuria and associated with a variable clinical phenotype: epileptic or convulsive attacks, dysmorphic features and severe developmental delay, and congenital microvillous atrophy.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8287R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8287R-A750
Lokale Artikelnummer::
BOSSBS-8287R-A750
Beschreibung:
Catalyzes the second step of the reductive pyrimidine degradation, the reversible hydrolytic ring opening of dihydropyrimidines. Can catalyzes the ring opening of 5,6-dihydrouracil to N-carbamyl-alanine and of 5,6-dihydrothymine to N-carbamyl-amino isobutyrate.Tissue specificity:Liver and kidney.Involvement in disease:Defects in DPYS are the cause of dihydropyrimidinase deficiency (DHPD). DHPD is an autosomal recessive disorder characterised by dihydropyrimidinuria and associated with a variable clinical phenotype: epileptic or convulsive attacks, dysmorphic features and severe developmental delay, and congenital microvillous atrophy.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13016R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13016R-HRP
Lokale Artikelnummer::
BOSSBS-13016R-HRP
Beschreibung:
DNA polymerase specifically involved in DNA repair. Plays an important role in translesion synthesis, where the normal high fidelity DNA polymerases cannot proceed and DNA synthesis stalls. Plays an important role in the repair of UV-induced pyrimidine dimers. Depending on the context, it inserts the correct base, but causes frequent base transitions and transversions. May play a role in hypermutation at immunoglobulin genes. Forms a Schiff base with 5'-deoxyribose phosphate at abasic sites, but does not have lyase activity. Targets POLI to replication foci.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4,6-Dihydroxy-5-methylpyrimidin
Artikel-Nr:
(BLDPBD2739-25G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD2739-25G
Lokale Artikelnummer::
BLDPBD2739-25G
Beschreibung:
4,6-Dihydroxy-2-methylpyrimidin 97%
VE:
1 * 25 g
Artikel-Nr:
(BLDPBD23022-500G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD23022-500G
Lokale Artikelnummer::
BLDPBD23022-500G
Beschreibung:
Phenyl-(4,6-dimethoxy-2-pyrimidinyl)carbamat 97%
VE:
1 * 500 g
Artikel-Nr:
(BOSSBS-8287R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8287R
Lokale Artikelnummer::
BOSSBS-8287R
Beschreibung:
Catalyzes the second step of the reductive pyrimidine degradation, the reversible hydrolytic ring opening of dihydropyrimidines. Can catalyzes the ring opening of 5,6-dihydrouracil to N-carbamyl-alanine and of 5,6-dihydrothymine to N-carbamyl-amino isobutyrate.Tissue specificity:Liver and kidney.Involvement in disease:Defects in DPYS are the cause of dihydropyrimidinase deficiency (DHPD). DHPD is an autosomal recessive disorder characterized by dihydropyrimidinuria and associated with a variable clinical phenotype: epileptic or convulsive attacks, dysmorphic features and severe developmental delay, and congenital microvillous atrophy.
VE:
1 * 100 µl
Lieferant:
Thermo Scientific
Beschreibung:
Pyrimidine-2-thiol
Artikel-Nr:
(BOSSBS-8287R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8287R-A680
Lokale Artikelnummer::
BOSSBS-8287R-A680
Beschreibung:
Catalyzes the second step of the reductive pyrimidine degradation, the reversible hydrolytic ring opening of dihydropyrimidines. Can catalyzes the ring opening of 5,6-dihydrouracil to N-carbamyl-alanine and of 5,6-dihydrothymine to N-carbamyl-amino isobutyrate.Tissue specificity:Liver and kidney.Involvement in disease:Defects in DPYS are the cause of dihydropyrimidinase deficiency (DHPD). DHPD is an autosomal recessive disorder characterised by dihydropyrimidinuria and associated with a variable clinical phenotype: epileptic or convulsive attacks, dysmorphic features and severe developmental delay, and congenital microvillous atrophy.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13016R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13016R-CY5
Lokale Artikelnummer::
BOSSBS-13016R-CY5
Beschreibung:
DNA polymerase specifically involved in DNA repair. Plays an important role in translesion synthesis, where the normal high fidelity DNA polymerases cannot proceed and DNA synthesis stalls. Plays an important role in the repair of UV-induced pyrimidine dimers. Depending on the context, it inserts the correct base, but causes frequent base transitions and transversions. May play a role in hypermutation at immunoglobulin genes. Forms a Schiff base with 5'-deoxyribose phosphate at abasic sites, but does not have lyase activity. Targets POLI to replication foci.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13016R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13016R-A350
Lokale Artikelnummer::
BOSSBS-13016R-A350
Beschreibung:
DNA polymerase specifically involved in DNA repair. Plays an important role in translesion synthesis, where the normal high fidelity DNA polymerases cannot proceed and DNA synthesis stalls. Plays an important role in the repair of UV-induced pyrimidine dimers. Depending on the context, it inserts the correct base, but causes frequent base transitions and transversions. May play a role in hypermutation at immunoglobulin genes. Forms a Schiff base with 5'-deoxyribose phosphate at abasic sites, but does not have lyase activity. Targets POLI to replication foci.
VE:
1 * 100 µl
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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