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1-[2-Oxo-2-(2-pyridyl)ethyl]pyridinium+iodide
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1-[2-Oxo-2-(2-pyridyl)ethyl]pyridinium+iodide
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Methyl 2-chloro-6-fluoro-3-methoxybenzoate 95%
Lieferant:
S.C.A.T.
Beschreibung:
Spezialadapter zum Anschliessen eines SCAT-Abluftfilters an die Kanister der Hersteller Justrite und CPC.
Artikel-Nr:
(BOSSBS-2940R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2940R-CY5
Lokale Artikelnummer::
BOSSBS-2940R-CY5
Beschreibung:
Alpha-L-fucosidase is responsible for hydrolyzing the alpha-1,6-linked fucose joined to the reducing-end N-acetylglucosamine of the carbohydrate moieties of glycoproteins.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
5-Bromo-1,4-dimethylimidazole 98%
Artikel-Nr:
(BOSSBS-3981R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3981R-A680
Lokale Artikelnummer::
BOSSBS-3981R-A680
Beschreibung:
FBP2 is a gluconeogenesis regulatory enzyme which catalyses the hydrolysis of fructose 1,6-bisphosphate to fructose 6-phosphate and inorganic phosphate.
VE:
1 * 100 µl
Artikel-Nr:
(H55596.06)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
H55596.06
Lokale Artikelnummer::
ALFAH55596.06
Beschreibung:
Tributylphenylzinn 97%
VE:
1 * 5 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Methyl-1H-1,2,3-triazole
Artikel-Nr:
(BOSSBS-9632R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9632R-A680
Lokale Artikelnummer::
BOSSBS-9632R-A680
Beschreibung:
PDZD9 (PDZ domain containing 9) is a 264 amino acid protein that contains one PDZ (DHR) domain and participates in protein binding. Conserved in chimpanzee, dog, cow, mouse and rat, PDZD9 exists as two alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 16p12.1. Chromosome 16 encodes over 900 genes, approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. Giant axonal neuropathy, a nervous system disorder characterised by increasing malfunction with growth, and the rare disorder Rubinstein-Taybi syndrome, characterised by mental retardation and predisposition to tumour growth and white blood cell neoplasias, are associated with chromosome 16. Crohn's disease, a gastrointestinal inflammatory condition, and systemic lupus erythematosis are also associated with chromosome 16.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9632R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9632R-A750
Lokale Artikelnummer::
BOSSBS-9632R-A750
Beschreibung:
PDZD9 (PDZ domain containing 9) is a 264 amino acid protein that contains one PDZ (DHR) domain and participates in protein binding. Conserved in chimpanzee, dog, cow, mouse and rat, PDZD9 exists as two alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 16p12.1. Chromosome 16 encodes over 900 genes, approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. Giant axonal neuropathy, a nervous system disorder characterised by increasing malfunction with growth, and the rare disorder Rubinstein-Taybi syndrome, characterised by mental retardation and predisposition to tumour growth and white blood cell neoplasias, are associated with chromosome 16. Crohn's disease, a gastrointestinal inflammatory condition, and systemic lupus erythematosis are also associated with chromosome 16.
VE:
1 * 100 µl
Artikel-Nr:
(APOSPC6120-25G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC6120-25G
Lokale Artikelnummer::
APOSPC6120-25G
Beschreibung:
Perfluoro(methyldecalin) 85%
VE:
1 * 25 g
Artikel-Nr:
(92178.010)
Lieferant:
VWR Chemicals
Lokale Artikelnummer::
VWRC92178.010
Beschreibung:
Organic Standard, Dechlorane 604 Component A, 50 µg/ml in toluene, Packung: Glass ampoule/vial
VE:
1 * 1 mL
Artikel-Nr:
(MILFMAWP025A0)
Lieferant:
Merck
Hersteller-Artikelnummer::
MAWP025A0
Lokale Artikelnummer::
MILFMAWP025A0
Beschreibung:
The PS monitor is used for sample collection and particle analysis. The PP monitor is used for microscopic particle analysis and sample collection for HPLC and UV detection.
VE:
1 * 50 ST
Lieferant:
BLD PHARMATECH GMBH
Beschreibung:
5-Fluorsalicylsäure 98%
Artikel-Nr:
(APOSOR928643-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR928643-1G
Lokale Artikelnummer::
APOSOR928643-1G
Beschreibung:
4-Methyl-1H-imidazole-2-carbaldehyde 95%
VE:
1 * 1 g
Artikel-Nr:
(BOSSBS-12039R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12039R-A555
Lokale Artikelnummer::
BOSSBS-12039R-A555
Beschreibung:
GDE1 is a 331 amino acid multi-pass membrane protein that localizes to both the membrane and the cytoplasm and contains one GDPD domain. Expressed in a wide variety of tissues, GDE1 uses magnesium as a cofactor to catalyze the conversion of 1-(sn-glycero-3-phospho)-1D-myo-inositol to myo-inositol and sn-glycerol 3-phosphate, an event that is modulated by G protein signaling pathways and provides a link between phosphoinositide metabolism and G protein signal transduction. The gene encoding GDE1 maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12039R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12039R-A647
Lokale Artikelnummer::
BOSSBS-12039R-A647
Beschreibung:
GDE1 is a 331 amino acid multi-pass membrane protein that localizes to both the membrane and the cytoplasm and contains one GDPD domain. Expressed in a wide variety of tissues, GDE1 uses magnesium as a cofactor to catalyze the conversion of 1-(sn-glycero-3-phospho)-1D-myo-inositol to myo-inositol and sn-glycerol 3-phosphate, an event that is modulated by G protein signaling pathways and provides a link between phosphoinositide metabolism and G protein signal transduction. The gene encoding GDE1 maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
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.
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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