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Methyl+2,4,5-trifluorobenzoate
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Methyl+2,4,5-trifluorobenzoate
Lieferant:
Brady
Beschreibung:
Diese Absperrvorrichtungen verhindern die unautorisierte Betätigung von Drucktasten und Notausschaltern.
Lieferant:
KEYSTONE CLEANROOM PRODUCTS
Beschreibung:
Schützt gereinigte, unsterile Produktionsschläuche vor externen Kontaminationsquellen.
Artikel-Nr:
(85032.270)
Lieferant:
VWR Chemicals
Lokale Artikelnummer::
VWRC85032.270
Beschreibung:
Bromwasserstoff 47%, NORMATOM®, ultrarein für die Spurenanalytik von Metallen
VE:
1 * 500 mL
Lieferant:
BECTON DICKINSON MEDICAL
Beschreibung:
Die Kanülen bestehen aus strahlenundurchlässigem FEP-Polymer und thermogeformten Materials.
Lieferant:
SI Analytics
Beschreibung:
Cannon-Fenske viscometers for automatic measurements especially in routine analyses.
Artikel-Nr:
(BLDPBD01212731-10M)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD01212731-10M
Lokale Artikelnummer::
BLDPBD01212731-10M
Beschreibung:
N-(3-Carbamoyl-4,5,6,7-tetrahydrobenzo[b]thiophen-2-yl)nicotinamide 98%
VE:
1 * 10 mg
Artikel-Nr:
(BOSSBS-9632R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9632R-FITC
Lokale Artikelnummer::
BOSSBS-9632R-FITC
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 characterized by increasing malfunction with growth, and the rare disorder Rubinstein-Taybi syndrome, characterized by mental retardation and predisposition to tumor 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-6805R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6805R-A555
Lokale Artikelnummer::
BOSSBS-6805R-A555
Beschreibung:
CLUAP1 (Clusterin associated protein 1) is a 413 amino acid nuclear protein that exists as two alternatively spliced isoforms that interact with Clusterin. CLUAP1 is suggested to play a role in apoptosis and cell proliferation, and is expressed in testis, thrachea and thyroid, with low levels found in adrenal gland and spinal cord. The gene encoding CLUAP1 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:
(67349-100ML)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
67349-100ML
Lokale Artikelnummer::
SUPL67349-100ML
Beschreibung:
Multi-Element Standard, Rare earth element mix for ICP, 50 mg/L, TraceCERT®, Supelco®, Matrix: 2% HNO₃, Anwendung: AAS-Standards, ICP-Standards
VE:
1 * 100 mL
Lieferant:
Thermo Fisher Scientific
Beschreibung:
HDPE, durchscheinend mit PP-Schraubverschluss
Artikel-Nr:
(BOSSBS-8320R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8320R-CY5.5
Lokale Artikelnummer::
BOSSBS-8320R-CY5.5
Beschreibung:
HEATR3 is a 680 amino acid protein existing as three alternatively spliced isoforms and containing two HEAT (Huntingtin, elongation factor 3 (EF3), protein phosphatase 2A (PP2A) and the yeast PI3-kinase Tor1) repeats. HEAT repeats form rod-like helical structures that are involved in intracellular transport. HEATR3 is encoded by a gene located on 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, a gastrointestinal inflammatory condition.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12039R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12039R-A488
Lokale Artikelnummer::
BOSSBS-12039R-A488
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)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12039R
Lokale Artikelnummer::
BOSSBS-12039R
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:
(APOSOR11232-5G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR11232-5G
Lokale Artikelnummer::
APOSOR11232-5G
Beschreibung:
3'-Nitropropiophenon
VE:
1 * 5 g
Lieferant:
Thermo Scientific
Beschreibung:
Lauroylchlorid 98%
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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