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(\u00B1)-1,2-Pentandiol


37 871  results were found

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Lieferant:  APOLLO SCIENTIFIC
Beschreibung:   4'-Nitro-3'-(trifluormethyl)acetanilid 97%
Lieferant:  APOLLO SCIENTIFIC
Beschreibung:   Methyl 2-bromo-5-fluoro-3-nitrobenzoate

Lieferant:  Alfa Aesar
Hersteller-Artikelnummer:: H52733.03
Lokale Artikelnummer:: ALFAH52733.03
Beschreibung:   trans-N-Boc-4-cyano-L-proline methyl ester 97%
VE:  1 * 1 g
Lieferant:  Brady
Beschreibung:   B-7569 vinyl is ideal for indoor/outdoor facility labels, including 5S labels, safety labels, warning labels, pipe markers, equipment labels and visual workplace labels.
Artikel-Nr: (MILFXX2702550)

Lieferant:  Merck
Hersteller-Artikelnummer:: XX2702550
Lokale Artikelnummer:: MILFXX2702550
Beschreibung:   Simultaneously vacuum filter 12 samples for rapid analysis of retentate or filtrate. Numbered positions on the filter plate assure accurate sample tracking. Sealing stoppers maintain vacuum on unused sample cups. Accessory extension barrels increase sample volumes from 15 to 50 ml.
VE:  1 * 1 ST

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-12093R-CY5
Lokale Artikelnummer:: BOSSBS-12093R-CY5
Beschreibung:   Cyclic nucleotide-gated (CNG) cation channels are heteromeric complexes made up of principal alpha and modulatory beta subunits (1,2). The alpha subunits consist of CNG1-3 and form functional cation channels by themselves (1,2). The beta subunits consist of CNG4-6 and, unlike the alpha subunits, do not form functional channels, but rather modify the properties of channels (1,2). CNG channels are essential components of olfactory and visual transduction (1,2). In olfactory neurons, CNG2, CNG4.3 and CNG5 form Ca2+ permeable channels, which open and depolarize the cell in response to cAMP (1-3). In rod photoreceptors, CNG1 and CNG4.1 combine to form Ca ion permeable channels, which give rise to a current in response to cGMP (1-3). CNG3 and CNG6 are expressed in cone receptors and may combine to form a native cGMP-activated channel (2,3). CNG channels have been implicated in other areas (4-6). CNG1 is also expressed in medium-sized and small-sized arteries, suggesting a role for CNG in the regulation of arterial blood pressure and of blood supply to different regions (4). CNG1, CNG4.1 and CNG4.2 have been detected in the rat pineal gland (5). CNG2, CNG4.3 and CNG5 are present in GT1 cell lines and may play a role in the secretion of gonadotropin-releasing hormone (6).
VE:  1 * 100 µl
Artikel-Nr: (APOSOR7584-250MG)

Lieferant:  APOLLO SCIENTIFIC
Hersteller-Artikelnummer:: OR7584-250MG
Lokale Artikelnummer:: APOSOR7584-250MG
Beschreibung:   3-(Thien-2-yl)aniline 96%
VE:  1 * 250 mg

Lieferant:  US Biological
Hersteller-Artikelnummer:: 129398
Lokale Artikelnummer:: USBI129398
Beschreibung:   Anti-MAPK12 Rabbit Polyclonal Antibody
VE:  1 * 100 µG

Lieferant:  APOLLO SCIENTIFIC
Hersteller-Artikelnummer:: OR32008-1G
Lokale Artikelnummer:: APOSOR32008-1G
Beschreibung:   N-Ethyl-5-(1-phenoxyethyl)-1H-pyrazole-1-carboxamide 95%
VE:  1 * 1 g

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-8302R-A647
Lokale Artikelnummer:: BOSSBS-8302R-A647
Beschreibung:   GLT8D2 (glycosyltransferase 8 domain-containing protein 2), also known as GALA4A, is a 349 amino acid single-pass type II membrane protein. A member of the glycosyltransferase 8 family, GLT8D2 is encoded by a gene that maps to human chromosome 12q23.3. Encoding over 1,100 genes within 132 million base pairs, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis, Noonan syndrome, Kniest dysplasia and trisomy 12p. Chromosome 12 is also home to a homeobox gene cluster, which encodes crucial transcription factors for morphogenesis, as well as the natural killer complex gene cluster, which encodes C-type lectin proteins that mediate the NK cell response to MHC I interaction.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-8302R-CY3
Lokale Artikelnummer:: BOSSBS-8302R-CY3
Beschreibung:   GLT8D2 (glycosyltransferase 8 domain-containing protein 2), also known as GALA4A, is a 349 amino acid single-pass type II membrane protein. A member of the glycosyltransferase 8 family, GLT8D2 is encoded by a gene that maps to human chromosome 12q23.3. Encoding over 1,100 genes within 132 million base pairs, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis, Noonan syndrome, Kniest dysplasia and trisomy 12p. Chromosome 12 is also home to a homeobox gene cluster, which encodes crucial transcription factors for morphogenesis, as well as the natural killer complex gene cluster, which encodes C-type lectin proteins that mediate the NK cell response to MHC I interaction.
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-8302R)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-8302R
Lokale Artikelnummer:: BOSSBS-8302R
Beschreibung:   GLT8D2 (glycosyltransferase 8 domain-containing protein 2), also known as GALA4A, is a 349 amino acid single-pass type II membrane protein. A member of the glycosyltransferase 8 family, GLT8D2 is encoded by a gene that maps to human chromosome 12q23.3. Encoding over 1,100 genes within 132 million base pairs, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis, Noonan syndrome, Kniest dysplasia and trisomy 12p. Chromosome 12 is also home to a homeobox gene cluster, which encodes crucial transcription factors for morphogenesis, as well as the natural killer complex gene cluster, which encodes C-type lectin proteins that mediate the NK cell response to MHC I interaction.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-8302R-A555
Lokale Artikelnummer:: BOSSBS-8302R-A555
Beschreibung:   GLT8D2 (glycosyltransferase 8 domain-containing protein 2), also known as GALA4A, is a 349 amino acid single-pass type II membrane protein. A member of the glycosyltransferase 8 family, GLT8D2 is encoded by a gene that maps to human chromosome 12q23.3. Encoding over 1,100 genes within 132 million base pairs, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis, Noonan syndrome, Kniest dysplasia and trisomy 12p. Chromosome 12 is also home to a homeobox gene cluster, which encodes crucial transcription factors for morphogenesis, as well as the natural killer complex gene cluster, which encodes C-type lectin proteins that mediate the NK cell response to MHC I interaction.
VE:  1 * 100 µl
Lieferant:  VWR Chemicals
Beschreibung:   Natrium-L(+)-ascorbat ≥99%, TECHNICAL

Lieferant:  Alfa Aesar
Hersteller-Artikelnummer:: 12889.09
Lokale Artikelnummer:: ALFA12889.09
Beschreibung:   Rubidiumnitrat ≥99,8% (Metall-Basis)
VE:  1 * 10 g
Lieferant:  APOLLO SCIENTIFIC
Beschreibung:   6-Bromo-2-(methylsulphonyl)-1,2,3,4-tetrahydroisoquinoline 95%
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 call 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 call 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.
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
Dieses Produkt wurde von Ihrer Organisation gesperrt. Bitte kontaktieren Sie Ihren Einkauf für weitere Informationen.
Dieses Produkt ist Ersatz für den von Ihnen gewünschten Artikel.
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