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1,3-Bis(3-aminopropyl)tetramethyldisiloxane


72 434  results were found

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Artikel-Nr: (MOLE20831626-25G)

Lieferant:  Molekula
Hersteller-Artikelnummer:: 20831626-25G
Lokale Artikelnummer:: MOLE20831626-25G
Beschreibung:   3-Amino-1H-1,2,4-triazol-5-thiol
VE:  1 * 25 g
Market Source Item This is a MarketSource item. Additional charges may apply
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

Lieferant:  Ludwig Schneider GmbH & CO. KG
Hersteller-Artikelnummer:: 3202004
Lokale Artikelnummer:: SCNL3202004
Beschreibung:   Diese kalibrierten Präzisions-Aräometer sind ohne Thermometer ausgeführt.
VE:  1 * 1 ST

Lieferant:  APOLLO SCIENTIFIC
Hersteller-Artikelnummer:: OR933048-25G
Lokale Artikelnummer:: APOSOR933048-25G
Beschreibung:   Pyrazolo[1,5-a]pyrimidin-7(4H)-one 25g pack 1 * 25 g
VE:  1 * 25 g
New Product
Lieferant:  FLUOROCHEM
Beschreibung:   6-Fluor-3-formylchromon
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
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
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
Lieferant:  Sigma-Aldrich
Beschreibung:   Isatosäureanhydrid, Sigma-Aldrich®
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:  Thermo Scientific
Beschreibung:   CAS No.: 7783-13-3
Lieferant:  Honeywell Chemicals
Hersteller-Artikelnummer:: 71283-1KG
Lokale Artikelnummer:: HONC71283-1KG
Beschreibung:   Natriumammoniumhydrogenphosphat Tetrahydrat ≥99,0% (durch nicht wässrige Titration), Puriss. p.a., Fluka™
VE:  1 * 1 kg
Lieferant:  APOLLO SCIENTIFIC
Beschreibung:   4,6-Dihydroxy-5-methylpyrimidin
Lieferant:  APOLLO SCIENTIFIC
Hersteller-Artikelnummer:: PC103462-1G
Lokale Artikelnummer:: APOSPC103462-1G
Beschreibung:   1-(4-Fluorophenyl)-1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one 1g pack 1 * 1 g
VE:  1 * 1 g
New Product
Preis auf Anfrage
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 call 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 call noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
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Dieses Produkt ist Ersatz für den von Ihnen gewünschten Artikel.
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