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Hai cercato: 3-Carbamyl-1-methylpyridinium+chloride


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Image Unavailable-BOSSBS-8287R-A750

Anti-Dihydropyrimidinase Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Codice catalogo: (BOSSBS-8287R-A750)
Fornitore: Bioss
Codice articolo fornitore: BS-8287R-A750
Codice articolo locale: BOSSBS-8287R-A750
Descrizione: 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8287R-FITC

Anti-DPYS Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Codice catalogo: (BOSSBS-8287R-FITC)
Fornitore: Bioss
Codice articolo fornitore: BS-8287R-FITC
Codice articolo locale: BOSSBS-8287R-FITC
Descrizione: 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8287R-HRP

Anti-DPYS Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Codice catalogo: (BOSSBS-8287R-HRP)
Fornitore: Bioss
Codice articolo fornitore: BS-8287R-HRP
Codice articolo locale: BOSSBS-8287R-HRP
Descrizione: 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.
UOM: 1 * 100 µl
Image Unavailable-TCIAC0906-25G

2-Chloro-1-methylpyridinium-p-toluenesulphonate ≥98.0% (by titrimetric analysis)

Codice catalogo: (TCIAC0906-25G)
Fornitore: TCI
Codice articolo fornitore: C0906-25G
Codice articolo locale: TCIAC0906-25G
Descrizione: 2-Chloro-1-methylpyridinium-p-toluenesulphonate ≥98.0% (by titrimetric analysis)
UOM: 1 * 25 g
Image Unavailable-L12072.14

N-Methylpyridinium-4-carboxaldehyde benzenesulphonate hydrate 97%

Fornitore: Thermo Fisher Scientific
Descrizione: N-Methylpyridinium-4-carboxaldehyde benzenesulphonate hydrate 97%

MSDS Certificati

Image Unavailable-ENZOBMLL1200005

1-O-Hexadecyl-2-N-methylcarbamyl-sn-glycero-3-phosphocholine ≥98% (by TLC)

Codice catalogo: (ENZOBMLL1200005)
Fornitore: ENZO LIFE SCIENCES
Codice articolo fornitore: BMLL1200005
Codice articolo locale: ENZOBMLL1200005
Descrizione: PAF receptor activator.
UOM: 1 * 5 mg

New Product


Image Unavailable-TCIAB3104-25G

1-Butyl-3-methylpyridinium bromide ≥98.0% (by HPLC, titration analysis)

Fornitore: TCI
Descrizione: 1-Butyl-3-methylpyridinium bromide ≥98.0% (by HPLC, titration analysis)

Image Unavailable-TCIAC0029-1G

N-Carbamoyl-DL-aspartic acid ≥98.0% (by titrimetric analysis)

Codice catalogo: (TCIAC0029-1G)
Fornitore: TCI
Codice articolo fornitore: C0029-1G
Codice articolo locale: TCIAC0029-1G
Descrizione: N-Carbamoyl-DL-aspartic acid ≥98.0% (by titrimetric analysis)
UOM: 1 * 1 g
Image Unavailable-BOSSBS-8287R-CY3

Anti-DPYS Rabbit Polyclonal Antibody (Cy3®)

Codice catalogo: (BOSSBS-8287R-CY3)
Fornitore: Bioss
Codice articolo fornitore: BS-8287R-CY3
Codice articolo locale: BOSSBS-8287R-CY3
Descrizione: 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8287R-CY5

Anti-DPYS Rabbit Polyclonal Antibody (Cy5®)

Codice catalogo: (BOSSBS-8287R-CY5)
Fornitore: Bioss
Codice articolo fornitore: BS-8287R-CY5
Codice articolo locale: BOSSBS-8287R-CY5
Descrizione: 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8287R-CY7

Anti-DPYS Rabbit Polyclonal Antibody (Cy7®)

Codice catalogo: (BOSSBS-8287R-CY7)
Fornitore: Bioss
Codice articolo fornitore: BS-8287R-CY7
Codice articolo locale: BOSSBS-8287R-CY7
Descrizione: 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8287R-CY5.5

Anti-DPYS Rabbit Polyclonal Antibody (Cy5.5®)

Codice catalogo: (BOSSBS-8287R-CY5.5)
Fornitore: Bioss
Codice articolo fornitore: BS-8287R-CY5.5
Codice articolo locale: BOSSBS-8287R-CY5.5
Descrizione: 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8287R

Anti-Dihydropyrimidinase Rabbit Polyclonal Antibody

Codice catalogo: (BOSSBS-8287R)
Fornitore: Bioss
Codice articolo fornitore: BS-8287R
Codice articolo locale: BOSSBS-8287R
Descrizione: 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8287R-A647

Anti-DPYS Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Codice catalogo: (BOSSBS-8287R-A647)
Fornitore: Bioss
Codice articolo fornitore: BS-8287R-A647
Codice articolo locale: BOSSBS-8287R-A647
Descrizione: 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8287R-A350

Anti-DPYS Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Codice catalogo: (BOSSBS-8287R-A350)
Fornitore: Bioss
Codice articolo fornitore: BS-8287R-A350
Codice articolo locale: BOSSBS-8287R-A350
Descrizione: 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.
UOM: 1 * 100 µl
Image Unavailable-TCIAA5014-1G

TMPyP [=α,β,γ,δ-tetrakis(1-methylpyridinium-4-yl)porphyrin-p-toluenesulphonate] ≥98.0% (by total nitrogen basis) per spettrofotometria

Fornitore: TCI
Descrizione: Ultra-high sensitive spectrophotometric reagent for Cu, Mg. Reagent or the simultaneous determination of metals by HPLC.

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La disponibilità per questo articolo è limitata, ma potrebbe essere disponibile in un magazzino vicino a voi. Si prega di assicurarsi che si è effettuato l'accesso al sito, in modo che ledisponibilità possano essere visualizzati. Se il call è ancora visualizzato e hai bisogno di assistenza, si prega di telefonare a 1-800-932 - 5000.
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