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8H-Indeno[1,2-c]thiophen-8-one
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8H-Indeno[1,2-c]thiophen-8-one
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3,4-Dimethoxybenzylalkohol 98%
Artikel-Nr:
(BOSSBS-12051R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12051R-FITC
Lokale Artikelnummer::
BOSSBS-12051R-FITC
Beschreibung:
This is one of the several different receptors for 5-hydroxytryptamine (serotonin), a biogenic hormone that functions as a neurotransmitter, a hormone, and a mitogen. This receptor is a ligand-gated ion channel, which when activated causes fast, depolarizing responses in neurons. It is a cation-specific, but otherwise relatively nonselective, ion channel.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8056R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8056R-A555
Lokale Artikelnummer::
BOSSBS-8056R-A555
Beschreibung:
KLHL14 is a member of the KLHL family. The kelch motif was initially discovered in Kelch. In this protein there are six copies of the motif. It has been shown for one member that it is related to Galactose Oxidase for which a structure has been solved. Two isoforms of this protein exist - 70kDa and 43kDa.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5082R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5082R-HRP
Lokale Artikelnummer::
BOSSBS-5082R-HRP
Beschreibung:
Lass5, or LAG1 longevity assurance homolog 5, is thought to be either a bona fide (dihydro)ceramide synthase or a modulator of its activity. When overexpressed in cells is involved in the production of sphingolipids containing mainly one fatty acid donnor ceramide) in a fumonisin B1-independent manner.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8056R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8056R-A488
Lokale Artikelnummer::
BOSSBS-8056R-A488
Beschreibung:
KLHL14 is a member of the KLHL family. The kelch motif was initially discovered in Kelch. In this protein there are six copies of the motif. It has been shown for one member that it is related to Galactose Oxidase for which a structure has been solved. Two isoforms of this protein exist - 70kDa and 43kDa.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11945R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11945R-HRP
Lokale Artikelnummer::
BOSSBS-11945R-HRP
Beschreibung:
Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf52 gene product has been provisionally designated C12orf52 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9948R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9948R-A680
Lokale Artikelnummer::
BOSSBS-9948R-A680
Beschreibung:
Encoding over 1100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf42 gene product has been provisionally designated C12orf42 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8229R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8229R-A350
Lokale Artikelnummer::
BOSSBS-8229R-A350
Beschreibung:
Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The FAM101A gene product has been provisionally designated FAM101A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9946R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9946R-A750
Lokale Artikelnummer::
BOSSBS-9946R-A750
Beschreibung:
Encoding over 1100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf29 gene product has been provisionally designated C12orf29 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9953R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9953R-A680
Lokale Artikelnummer::
BOSSBS-9953R-A680
Beschreibung:
Encoding over 1100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf61 gene product has been provisionally designated C12orf61 pending further characterisation.
VE:
1 * 100 µl
Lieferant:
ANSELL HEALTH CARE
Beschreibung:
Diese gestrickten Nylon-Handschuhe verfügen über eine Nitrilschaumbeschichtung an der Innenhand.
Artikel-Nr:
(BLDPBD15063-10G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD15063-10G
Lokale Artikelnummer::
BLDPBD15063-10G
Beschreibung:
3,4-Difluorbenzophenon 98%
VE:
1 * 10 g
Artikel-Nr:
(BOSSBS-5049R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5049R-CY5.5
Lokale Artikelnummer::
BOSSBS-5049R-CY5.5
Beschreibung:
Catalyzes the first step in the oxidation of the side chain of sterol intermediates; the 27-hydroxylation of 5-beta-cholestane-3-alpha,7-alpha,12-alpha-triol. Has also a vitamin D3-25-hydroxylase activity.
VE:
1 * 100 µl
Artikel-Nr:
(1.10648.0001)
Lieferant:
Merck
Hersteller-Artikelnummer::
1.10648.0001
Lokale Artikelnummer::
MERC1.10648.0001
Beschreibung:
MQuant® (MQ) Teststäbchen stellen ein Labor auf nur wenigen Quadratmillimetern dar. Als Screening-Verfahren bieten die Teststäbchen dem Anwender einen raschen Überblick darüber, ob und welche weiterführende Analysen notwendig sind. Diese gezielte Vorauswahl hilft viele zeit- und kostenaufwendige Analysen einzusparen. Die Stäbchen, die aus einer biologisch abbaubaren Polyesterfolie bestehen sowie der geringe Reagenzieninhalt in den Reaktionszonen ermöglichen eine problemlose Entsorgung.
VE:
1 * 100 Tests
Lieferant:
Brady
Beschreibung:
FreezerBondz™ Etiketten sind aus sehr flachem Material. Sie können sowohl auf gefrorenen Oberflächen als auch bei Raumtemperatur auf Flächen, die in Flüssigstickstoff (-196 °C) gelagert werden, angebracht werden. Lichtundurchlässig genug, um den HIPAA-Anforderungen zum Schutz von Patienteninformationen zu entsprechen.
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Brom-2-(4-morpholino)pyridin 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.
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