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Lieferant: 3M
Beschreibung: Leichte, stilvoll gestaltete Schutzbrille Die Virtua™ AP-Schutzbrille verfügt über ein stromlinienförmiges Rundum-Design für hervorragende Abdeckung und ein gutes Sichtfeld.

Artikel-Nr: (BOSSBS-11715R-CY3)
Lieferant: Bioss
Beschreibung: CLN8, a 286 amino acid transmembrane protein, localizes mainly to the endoplasmic reticulum, but also partially to the ER-Golgi intermediate compartment (ERGIC). Mutations in the CLN8 gene cause neuronal ceroid lipofuscinosis 8 and progressive epilepsy with mental retardation (EPMR). Both disorders are forms of neuronal ceroid-lipofuscinose (NCL), a group of progressive neurodegenerative diseases found in children, characterized by failure of psychomotor development, impaired vision, seizures and premature death. The CLN8 protein is one of eight proteins in the CLN family, including CLN1-CLN7, which are associated with NCL.
VE: 1 * 100 µl


Artikel-Nr: (BOSSBS-11715R-FITC)
Lieferant: Bioss
Beschreibung: CLN8, a 286 amino acid transmembrane protein, localizes mainly to the endoplasmic reticulum, but also partially to the ER-Golgi intermediate compartment (ERGIC). Mutations in the CLN8 gene cause neuronal ceroid lipofuscinosis 8 and progressive epilepsy with mental retardation (EPMR). Both disorders are forms of neuronal ceroid-lipofuscinose (NCL), a group of progressive neurodegenerative diseases found in children, characterized by failure of psychomotor development, impaired vision, seizures and premature death. The CLN8 protein is one of eight proteins in the CLN family, including CLN1-CLN7, which are associated with NCL.
VE: 1 * 100 µl


Artikel-Nr: (BOSSBS-11715R-CY5)
Lieferant: Bioss
Beschreibung: CLN8, a 286 amino acid transmembrane protein, localizes mainly to the endoplasmic reticulum, but also partially to the ER-Golgi intermediate compartment (ERGIC). Mutations in the CLN8 gene cause neuronal ceroid lipofuscinosis 8 and progressive epilepsy with mental retardation (EPMR). Both disorders are forms of neuronal ceroid-lipofuscinose (NCL), a group of progressive neurodegenerative diseases found in children, characterized by failure of psychomotor development, impaired vision, seizures and premature death. The CLN8 protein is one of eight proteins in the CLN family, including CLN1-CLN7, which are associated with NCL.
VE: 1 * 100 µl


Artikel-Nr: (BOSSBS-11715R-A680)
Lieferant: Bioss
Beschreibung: CLN8, a 286 amino acid transmembrane protein, localizes mainly to the endoplasmic reticulum, but also partially to the ER-Golgi intermediate compartment (ERGIC). Mutations in the CLN8 gene cause neuronal ceroid lipofuscinosis 8 and progressive epilepsy with mental retardation (EPMR). Both disorders are forms of neuronal ceroid-lipofuscinose (NCL), a group of progressive neurodegenerative diseases found in children, characterised by failure of psychomotor development, impaired vision, seizures and premature death. The CLN8 protein is one of eight proteins in the CLN family, including CLN1-CLN7, which are associated with NCL.
VE: 1 * 100 µl


Artikel-Nr: (MMMASCCS07SGAF-GRN)
Lieferant: 3M
Beschreibung: 3M™ Solus™ CCS-Sicherheitsbrillen sind randlose Schutzbrillen mit limettengrünen Bügeln und einem Corded Control System (CCS) zum Anbringen von Ohrstöpseln mit Kabel. Die Linse aus Polycarbonat verfügt auf beiden Seiten über eine Scotchgard™ Antibeschlag- und Antikratzbeschichtung für längere Haltbarkeit und bessere Sicht.
VE: 1 * 1 ST


Artikel-Nr: (111-1841)
Lieferant: VWR Collection
Beschreibung: Moderne Vollsichtbrille, die speziell für schmale Gesichtsformen konzipiert wurde. Sie besteht aus einer PC-Scheibe, einem PVC-Rahmen und einem Polyester/Gummi-Kopfband und ermöglicht einen exzellenten Rundumblick.
VE: 1 * 1 ST


Artikel-Nr: (BOSSBS-11332R-CY7)
Lieferant: Bioss
Beschreibung: Glutamic acid rich protein (GARP) is a soluble protein localized to the outer segments of the rod photoreceptor. It forms a subunit of cyclic nucleotide-gated (CNG) channels, nonselective cation channels, which play important roles in both visual and olfactory signal transduction. When associated with CNGA1, it is involved in the regulation of ion flow into the rod photoreceptor outer segment (ROS), in response to light-induced alteration of the levels of intracellular cGMP. There are 3 isoforms produced by alternative splicing. Isoform GARP2 is a high affinity rod photoreceptor phosphodiesterase (PDE6)-binding protein that modulates its catalytic properties; it is a regulator of spontaneous activation of rod PDE6, thereby serving to lower rod photoreceptor 'dark noise' and allowing these sensory cells to operate at the single photon detection limit. Defects in GARP are the cause of retinitis pigmentosa type 25 (RP25). RP leads to degeneration of retinal photoreceptor cells. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well.
VE: 1 * 100 µl


Artikel-Nr: (BOSSBS-11332R-CY5)
Lieferant: Bioss
Beschreibung: Glutamic acid rich protein (GARP) is a soluble protein localized to the outer segments of the rod photoreceptor. It forms a subunit of cyclic nucleotide-gated (CNG) channels, nonselective cation channels, which play important roles in both visual and olfactory signal transduction. When associated with CNGA1, it is involved in the regulation of ion flow into the rod photoreceptor outer segment (ROS), in response to light-induced alteration of the levels of intracellular cGMP. There are 3 isoforms produced by alternative splicing. Isoform GARP2 is a high affinity rod photoreceptor phosphodiesterase (PDE6)-binding protein that modulates its catalytic properties; it is a regulator of spontaneous activation of rod PDE6, thereby serving to lower rod photoreceptor 'dark noise' and allowing these sensory cells to operate at the single photon detection limit. Defects in GARP are the cause of retinitis pigmentosa type 25 (RP25). RP leads to degeneration of retinal photoreceptor cells. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well.
VE: 1 * 100 µl


Artikel-Nr: (BOSSBS-11332R-A488)
Lieferant: Bioss
Beschreibung: Glutamic acid rich protein (GARP) is a soluble protein localized to the outer segments of the rod photoreceptor. It forms a subunit of cyclic nucleotide-gated (CNG) channels, nonselective cation channels, which play important roles in both visual and olfactory signal transduction. When associated with CNGA1, it is involved in the regulation of ion flow into the rod photoreceptor outer segment (ROS), in response to light-induced alteration of the levels of intracellular cGMP. There are 3 isoforms produced by alternative splicing. Isoform GARP2 is a high affinity rod photoreceptor phosphodiesterase (PDE6)-binding protein that modulates its catalytic properties; it is a regulator of spontaneous activation of rod PDE6, thereby serving to lower rod photoreceptor 'dark noise' and allowing these sensory cells to operate at the single photon detection limit. Defects in GARP are the cause of retinitis pigmentosa type 25 (RP25). RP leads to degeneration of retinal photoreceptor cells. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well.
VE: 1 * 100 µl


Lieferant: VWR Collection
Beschreibung: Diese Kaltlichtquelle mit kompaktem und stabilem Aluminiumgehäuse und temperaturgeregeltem Lüfter liefert eine optimale und homogene Ausleuchtung der Lichtleiter. Sie eignet sich daher ideal für Hochgeschwindigkeitsaufnahmen in einer Vielzahl von Anwendungsbereichen wie Qualitätssicherung, industrielle Endoskopie und Bildverarbeitung sowie Reinraum-Anwendungen. Die Helligkeit übersteigt bei weitem die Helligkeit einer herkömmlichen 250-W-Halogen-Lichtquelle. Voraussichtliche LED-Lebensdauer von 50000 Stunden.

Artikel-Nr: (BOSSBS-11715R-A555)
Lieferant: Bioss
Beschreibung: CLN8, a 286 amino acid transmembrane protein, localizes mainly to the endoplasmic reticulum, but also partially to the ER-Golgi intermediate compartment (ERGIC). Mutations in the CLN8 gene cause neuronal ceroid lipofuscinosis 8 and progressive epilepsy with mental retardation (EPMR). Both disorders are forms of neuronal ceroid-lipofuscinose (NCL), a group of progressive neurodegenerative diseases found in children, characterized by failure of psychomotor development, impaired vision, seizures and premature death. The CLN8 protein is one of eight proteins in the CLN family, including CLN1-CLN7, which are associated with NCL.
VE: 1 * 100 µl


Artikel-Nr: (BOSSBS-13507R-CY5)
Lieferant: Bioss
Beschreibung: G protein-coupled receptors (GPCRs), also designated seven transmembrane (7TM) receptors and heptahelical receptors, are a protein family which interact with G proteins (heterotrimeric GTPases) to synthesize intracellular second messengers such as diacylglycerol, cyclic AMP, inositol phosphates, and calcium ions. Their diverse biological functions range from vision and olfaction to neuronal and endocrine signaling and are involved in many pathological conditions. G protein receptor 84 (GPR84), a member of the GCPR 1 family, is an orphan GCPR expressed in bone marrow, brain, heart, muscle, colon, thymus, spleen, kidney, liver, placenta, intestine, lung and peripheral blood leukocytes. In activated T cells, GPR84 regulates early interleukin-4 (IL-4) gene expression.
VE: 1 * 100 µl


Artikel-Nr: (BOSSBS-13518R-CY5)
Lieferant: Bioss
Beschreibung: G protein-coupled receptors (GPCRs), also designated seven transmembrane (7TM) receptors and heptahelical receptors, are a protein family which interact with G proteins (heterotrimeric GTPases) to synthesize intracellular second messengers such as diacylglycerol, cyclic AMP, inositol phosphates, and calcium ions. Their diverse biological functions range from vision and olfaction to neuronal and endocrine signaling and are involved in many pathological conditions. G protein receptor 128 (GPR128), a member of the secretin family of GCPRs with a GPS domain in its N-terminal domain, may mediate signaling processes to the interior of the cell via activation of G proteins. GPR128 represents an allopeptide which may be involved in T cell mediated transplant rejection as it is able to stimulate 2.102 T cells.
VE: 1 * 100 µl


Artikel-Nr: (BOSSBS-13517R-CY5)
Lieferant: Bioss
Beschreibung: G protein-coupled receptors (GPCRs), also designated seven transmembrane (7TM) receptors and heptahelical receptors, are a protein family which interact with G proteins (heterotrimeric GTPases) to synthesize intracellular second messengers such as diacylglycerol, cyclic AMP, inositol phosphates, and calcium ions. Their diverse biological functions range from vision and olfaction to neuronal and endocrine signaling and are involved in many pathological conditions. G protein receptor 128 (GPR128), a member of the secretin family of GCPRs with a GPS domain in its N-terminal domain, may mediate signaling processes to the interior of the cell via activation of G proteins. GPR128 represents an allopeptide which may be involved in T cell mediated transplant rejection as it is able to stimulate 2.102 T cells.
VE: 1 * 100 µl


Lieferant: VWR Collection
Beschreibung: Diese lüfterlose Kaltlichtquelle mit passiver Kühlung und kompaktem, stabilem Aluminiumgehäuse liefert eine optimale und homogene Ausleuchtung der Lichtleiter. Sie eignet sich daher ideal für Hochgeschwindigkeitsaufnahmen in einer Vielzahl von Anwendungsbereichen wie Qualitätssicherung, industrielle Endoskopie und Bildverarbeitung sowie Reinraum-Anwendungen. Die Helligkeit übersteigt bei weitem die Helligkeit einer herkömmlichen 250-W-Halogen-Lichtquelle. Voraussichtliche LED-Lebensdauer 50000 Stunden.

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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.
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