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Wyszukano: 5,6-Dimethoxynicotinaldehyde


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Numer katalogowy: (BOSSBS-8287R-A647)
Producent: Bioss
Opis: 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.
j.m.: 1 * 100 µl


Numer katalogowy: (BOSSBS-8287R-A350)
Producent: Bioss
Opis: 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.
j.m.: 1 * 100 µl


Numer katalogowy: (BOSSBS-8287R-FITC)
Producent: Bioss
Opis: 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.
j.m.: 1 * 100 µl


Numer katalogowy: (BOSSBS-8287R-HRP)
Producent: Bioss
Opis: 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.
j.m.: 1 * 100 µl


Numer katalogowy: (BOSSBS-8287R-A750)
Producent: Bioss
Opis: 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.
j.m.: 1 * 100 µl


Numer katalogowy: (BOSSBS-8287R)
Producent: Bioss
Opis: 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.
j.m.: 1 * 100 µl


Numer katalogowy: (BOSSBS-8287R-A488)
Producent: Bioss
Opis: 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.
j.m.: 1 * 100 µl


Numer katalogowy: (ROCK200-341-268)
Producent: Rockland Immunochemicals
Opis: This monoclonal antibody is suitable for immunofluorescence microscopy, FLISA and western blotting. Expect a band approximately 56 kDa in size corresponding to phosphorylated AKT Protein by western blotting in the appropriate cell lysate or extract.
j.m.: 1 * 100 µG


Numer katalogowy: (ROCK200-343-268)
Producent: Rockland Immunochemicals
Opis: This monoclonal antibody is suitable for immunofluorescence microscopy, FLISA and western blotting. Expect a band approximately 56 kDa in size corresponding to phosphorylated AKT Protein by western blotting in the appropriate cell lysate or extract.
j.m.: 1 * 100 µG


Numer katalogowy: (ROCK200-301-269S)
Producent: Rockland Immunochemicals
Opis: Anti-AKT pT308 antibody is suitable for ELISA, immunochemistry, immunoprecipitation and western blotting.  Expect a band approximately 56 kDa in size corresponding to phosphorylated AKT Protein by western blotting in the appropriate cell lysate.
j.m.: 1 * 25 µl


Numer katalogowy: (466-0476)
Producent: Binder
Opis: Z naturalną konwekcją, suszarki i komory temperaturowe Avantgarde.Line oferują jakość i niezawodność procesu. Posiadają szeroki zakres temperatury do 300 °C i mogą być używane we wszystkich zastosowaniach. Przez krótki czas nagrzewania i dużą moc są idealne do stosowania w nauce, badaniach i przemyśle. Technologia wstępnej komory podgrzewania APT.line™ daje jednorodny rozkład temperatury oraz doskonałą jednorodność temperatury. Jednostki do 115 litrów mogą być układane jedna na drugiej w celu zaoszczędzenia miejsca. Jednostki mają 60 mm grubości, co obniża zużycie energii i zwiększa wydajność. Wszystkie modele posiadają komorę ze stali nierdzewnej, z ergonomicznym systemem otwierania drzwi.
j.m.: 1 * 1 SZT


Numer katalogowy: (ROCK200-341-269)
Producent: Rockland Immunochemicals
Opis: This monoclonal antibody is suitable for immunofluorescence microscopy, FLISA and western blotting. Expect a band approximately 56 kDa in size corresponding to phosphorylated AKT Protein by western blotting in the appropriate cell lysate or extract.
j.m.: 1 * 100 µG


Numer katalogowy: (BOSSBS-8287R-A555)
Producent: Bioss
Opis: 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.
j.m.: 1 * 100 µl


Numer katalogowy: (ROCK200-308-I51)
Producent: Rockland Immunochemicals
Opis: Anti-AKT1 PE Antibody is suitable for Flow Cytometry, ELISA, immunochemistry, and western blotting. Expect a band approximately 56 kDa in size corresponding to AKT1 Protein by western blotting in the appropriate cell lysate or extract.
j.m.: 1 * 50 µG


Numer katalogowy: (ROCK200-326-E75)
Producent: Rockland Immunochemicals
Opis: Anti-AKT3 APC Antibody is suitable for Flow Cytometry, ELISA, immunochemistry, and western blotting. Expect a band approximately 56 kDa in size corresponding to AKT3 Protein by western blotting in the appropriate cell lysate or extract.
j.m.: 1 * 50 µG


Numer katalogowy: (ROCK200-308-E75)
Producent: Rockland Immunochemicals
Opis: Anti-AKT3 PE Antibody is suitable for Flow Cytometry, ELISA, immunochemistry, and western blotting. Expect a band approximately 56 kDa in size corresponding to AKT3 Protein by western blotting in the appropriate cell lysate or extract.
j.m.: 1 * 50 µG


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Zapasy tego artykułu są ograniczone, ale możliwe, że jest on dostępny w pobliskim magazynie. Upewnij się, że jesteś zalogowany na stronie, aby móc sprawdzić dostępność zapasów. Jeśli call ciągle się wyświetla i potrzebujesz pomocy, zadzwoń na 58 323 82 00.
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