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2-(2,4-Dichlorphenoxy)anilin+Hydrochlorid


26 346  results were found

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Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-2960R-A555
Lokale Artikelnummer:: BOSSBS-2960R-A555
Beschreibung:   Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. It is activated by internal ATP and probably plays an important role in potassium homeostasis. The encoded protein has a greater tendency to allow potassium to flow into a cell rather than out of a cell. Mutations in this gene have been associated with antenatal Bartter syndrome, which is characterized by salt wasting, hypokalemic alkalosis, hypercalciuria, and low blood pressure. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].
VE:  1 * 100 µl
Lieferant:  CHEMPUR SILANE
Beschreibung:   N,O-Bis(trimethylsilyl)trifluoracetamid
Artikel-Nr: (FLUO002143-100G)

Lieferant:  FLUOROCHEM
Hersteller-Artikelnummer:: 002143-100G
Lokale Artikelnummer:: FLUO002143-100G
Beschreibung:   2-Brom-5-(trifluormethyl)anilin
VE:  1 * 100 g
Market Source Item This is a MarketSource item. Additional charges may apply
Lieferant:  APOLLO SCIENTIFIC
Beschreibung:   Cyanimidodithiocarbonic acidmonomethyl ester monopotassium salt 95%
Lieferant:  Thermo Scientific
Beschreibung:   4-Chlor-3-iodbenzotrifluorid
Lieferant:  FLUOROCHEM
Beschreibung:   4-Chlor-3-nitrobenzotrifluorid
Lieferant:  FLUOROCHEM
Beschreibung:   4-Brom-2-(trifluormethyl)anilin
Lieferant:  Abcam
Hersteller-Artikelnummer:: AB274883-100
Lokale Artikelnummer:: ABCAAB274883-100
Beschreibung:   Anti-Sodium Potassium ATPase Rabbit Monoclonal Antibody [clone: EP1845Y] (Alexa Fluor® 555)
VE:  1 * 100 µl
Market Source Item This is a MarketSource item. Additional charges may apply

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-6760R-A647
Lokale Artikelnummer:: BOSSBS-6760R-A647
Beschreibung:   Probably important in cardiac repolarization. Associates with KCNE1 (MinK) to form the I(Ks) cardiac potassium current. Elicits a rapidly activating, potassium-selective outward current. Muscarinic agonist oxotremorine-M strongly suppresses KCNQ1/KCNE1 current in CHO cells in which cloned KCNQ1/KCNE1 channels were coexpressed with M1 muscarinic receptors. May associate also with KCNE3 (MiRP2) to form the potassium channel that is important for cyclic AMP-stimulated intestinal secretion of chloride ions, which is reduced in cystic fibrosis and pathologically stimulated in cholera and other forms of secretory diarrhea.
VE:  1 * 100 µl
Lieferant:  Sigma-Aldrich
Hersteller-Artikelnummer:: CRM498-100G
Lokale Artikelnummer:: SUPLCRM498-100G
Beschreibung:   pH/Conductivity CRM - clay soil, Supelco®
VE:  1 * 100 g
Artikel-Nr: (BOSSBS-11728R-CY7)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11728R-CY7
Lokale Artikelnummer:: BOSSBS-11728R-CY7
Beschreibung:   Epilepsy affects about 0.5% of the world’s population and has a large genetic component. Epilepsy results from an electrical hyperexcitability in the central nervous system. Potassium channels are important regulators of electrical signaling, determining the firing properties and responsiveness of a variety of neurons. Benign familial neonatal convulsions (BFNC), an autosomal dominant epilepsy of infancy, has been shown to be caused by mutations in the KCNQ2 or the KCNQ3 potassium channel genes. KCNQ2 and KCNQ3 are voltage-gated potassium channel proteins with six putative transmembrane domains. Both proteins display a broad distribution within the brain, with expression patterns that largely overlap.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11728R-A350
Lokale Artikelnummer:: BOSSBS-11728R-A350
Beschreibung:   Epilepsy affects about 0.5% of the world’s population and has a large genetic component. Epilepsy results from an electrical hyperexcitability in the central nervous system. Potassium channels are important regulators of electrical signaling, determining the firing properties and responsiveness of a variety of neurons. Benign familial neonatal convulsions (BFNC), an autosomal dominant epilepsy of infancy, has been shown to be caused by mutations in the KCNQ2 or the KCNQ3 potassium channel genes. KCNQ2 and KCNQ3 are voltage-gated potassium channel proteins with six putative transmembrane domains. Both proteins display a broad distribution within the brain, with expression patterns that largely overlap.
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-11728R-CY5)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11728R-CY5
Lokale Artikelnummer:: BOSSBS-11728R-CY5
Beschreibung:   Epilepsy affects about 0.5% of the world’s population and has a large genetic component. Epilepsy results from an electrical hyperexcitability in the central nervous system. Potassium channels are important regulators of electrical signaling, determining the firing properties and responsiveness of a variety of neurons. Benign familial neonatal convulsions (BFNC), an autosomal dominant epilepsy of infancy, has been shown to be caused by mutations in the KCNQ2 or the KCNQ3 potassium channel genes. KCNQ2 and KCNQ3 are voltage-gated potassium channel proteins with six putative transmembrane domains. Both proteins display a broad distribution within the brain, with expression patterns that largely overlap.
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-11728R)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11728R
Lokale Artikelnummer:: BOSSBS-11728R
Beschreibung:   Epilepsy affects about 0.5% of the world’s population and has a large genetic component. Epilepsy results from an electrical hyperexcitability in the central nervous system. Potassium channels are important regulators of electrical signaling, determining the firing properties and responsiveness of a variety of neurons. Benign familial neonatal convulsions (BFNC), an autosomal dominant epilepsy of infancy, has been shown to be caused by mutations in the KCNQ2 or the KCNQ3 potassium channel genes. KCNQ2 and KCNQ3 are voltage-gated potassium channel proteins with six putative transmembrane domains. Both proteins display a broad distribution within the brain, with expression patterns that largely overlap.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11728R-A488
Lokale Artikelnummer:: BOSSBS-11728R-A488
Beschreibung:   Epilepsy affects about 0.5% of the world’s population and has a large genetic component. Epilepsy results from an electrical hyperexcitability in the central nervous system. Potassium channels are important regulators of electrical signaling, determining the firing properties and responsiveness of a variety of neurons. Benign familial neonatal convulsions (BFNC), an autosomal dominant epilepsy of infancy, has been shown to be caused by mutations in the KCNQ2 or the KCNQ3 potassium channel genes. KCNQ2 and KCNQ3 are voltage-gated potassium channel proteins with six putative transmembrane domains. Both proteins display a broad distribution within the brain, with expression patterns that largely overlap.
VE:  1 * 100 µl
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11728R-HRP
Lokale Artikelnummer:: BOSSBS-11728R-HRP
Beschreibung:   Epilepsy affects about 0.5% of the world’s population and has a large genetic component. Epilepsy results from an electrical hyperexcitability in the central nervous system. Potassium channels are important regulators of electrical signaling, determining the firing properties and responsiveness of a variety of neurons. Benign familial neonatal convulsions (BFNC), an autosomal dominant epilepsy of infancy, has been shown to be caused by mutations in the KCNQ2 or the KCNQ3 potassium channel genes. KCNQ2 and KCNQ3 are voltage-gated potassium channel proteins with six putative transmembrane domains. Both proteins display a broad distribution within the brain, with expression patterns that largely overlap.
VE:  1 * 100 µl
Preis auf Anfrage
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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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