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2-Chloro-N-[4-(trifluoromethyl)phenyl]acetamide
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2-Chloro-N-[4-(trifluoromethyl)phenyl]acetamide
Lieferant:
ANSELL HEALTH CARE
Beschreibung:
These interlock cotton liners feature a ³/₄ dipped natural rubber latex coating and a knitwrist cuff. They provide good cut resistance.
Artikel-Nr:
(BOSSBS-11896R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11896R-FITC
Lokale Artikelnummer::
BOSSBS-11896R-FITC
Beschreibung:
NETO2 is a 525 amino acid single-pass type I membrane protein that contains two CUB domains and one LDL-receptor class A domain. Expressed as multiple alternatively spliced isoforms, NETO2 is thought to play a role in the development and maintenance of neuronal circuitry, possibly playing a role in proper brain function. The gene encoding NETO2 maps to human chromosome 16, which is associated with a variety of genetic disorders, 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 associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11896R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11896R-A555
Lokale Artikelnummer::
BOSSBS-11896R-A555
Beschreibung:
NETO2 is a 525 amino acid single-pass type I membrane protein that contains two CUB domains and one LDL-receptor class A domain. Expressed as multiple alternatively spliced isoforms, NETO2 is thought to play a role in the development and maintenance of neuronal circuitry, possibly playing a role in proper brain function. The gene encoding NETO2 maps to human chromosome 16, which is associated with a variety of genetic disorders, 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 associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9632R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9632R-CY5.5
Lokale Artikelnummer::
BOSSBS-9632R-CY5.5
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-5841R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5841R-A488
Lokale Artikelnummer::
BOSSBS-5841R-A488
Beschreibung:
MGAT5 is a mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase, a glycosyltransferase involved in the synthesis of protein-bound and lipid-bound oligosaccharides. Alterations of the oligosaccharides on cell surface glycoproteins cause significant changes in the adhesive or migratory behavior of a cell. Increase in the encoded protein's activity may correlate with the progression of invasive malignancies.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
1-(4-Pyridinyl)aceton 98%
Artikel-Nr:
(BOSSBS-9632R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9632R-A350
Lokale Artikelnummer::
BOSSBS-9632R-A350
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
Lieferant:
Alfa Aesar
Beschreibung:
Hydrobromic acid is an indispensable raw material for organic intermediates, inorganic pharmaceuticals, photosensitive materials, dyes and medicines. It is also used in the production of bromine compounds
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-Bromo-5-iodobenzal fluoride
Artikel-Nr:
(APOSOR200157-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR200157-1G
Lokale Artikelnummer::
APOSOR200157-1G
Beschreibung:
4-(4-Bromophenyl)butan-2-ol
VE:
1 * 1 g
Artikel-Nr:
(BOSSBS-5841R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5841R-A750
Lokale Artikelnummer::
BOSSBS-5841R-A750
Beschreibung:
MGAT5 is a mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase, a glycosyltransferase involved in the synthesis of protein-bound and lipid-bound oligosaccharides. Alterations of the oligosaccharides on cell surface glycoproteins cause significant changes in the adhesive or migratory behavior of a cell. Increase in the encoded protein's activity may correlate with the progression of invasive malignancies.
VE:
1 * 100 µl
Lieferant:
Thermo Fisher Scientific
Beschreibung:
Die neue Generation von Spitzen bietet hohe Flexibilität.
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-Bromophenylsulphur pentafluoride 98%
Artikel-Nr:
(BOSSBS-12039R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12039R-A680
Lokale Artikelnummer::
BOSSBS-12039R-A680
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 catalyse 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 Signalling 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 characterised 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-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12039R-A750
Lokale Artikelnummer::
BOSSBS-12039R-A750
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 catalyse 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 Signalling 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 characterised 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
Lieferant:
Lenz Laborglas GmbH & CO.KG
Beschreibung:
DURAN® Borosilikatglas.
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
 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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Dieses Produkt ist Ersatz für den von Ihnen gewünschten Artikel.
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