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Hai cercato: Potassium+cyclopentylmethyltrifluoroborate


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Codice catalogo: (ICNA0219031101)
Fornitore: MP Biomedicals
Codice articolo fornitore: 0219031101
Codice articolo locale: ICNA0219031101
Descrizione: Dissolves readily at 5 mg/ml in 0,05 M sodium/potassium phosphate pH 7,0 giving a clear green solution.
UOM: 1 * 1 Mu

MSDS


Codice catalogo: (BOSSBS-1815R-A647)
Fornitore: Bioss
Codice articolo fornitore: BS-1815R-A647
Codice articolo locale: BOSSBS-1815R-A647
Descrizione: Pore-forming (alpha) subunit of voltage-gated inwardly rectifying potassium channel. Channel properties are modulated by cAMP and subunit assembly. Mediates the rapidly activating component of the delayed rectifying potassium current in heart (IKr). Isoforms USO have no channel activity by themself, but modulates channel characteristics by forming heterotetramers with other isoforms which are retained intracellularly and undergo ubiquitin-dependent degradation.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-1815R-HRP)
Fornitore: Bioss
Codice articolo fornitore: BS-1815R-HRP
Codice articolo locale: BOSSBS-1815R-HRP
Descrizione: Pore-forming (alpha) subunit of voltage-gated inwardly rectifying potassium channel. Channel properties are modulated by cAMP and subunit assembly. Mediates the rapidly activating component of the delayed rectifying potassium current in heart (IKr). Isoforms USO have no channel activity by themself, but modulates channel characteristics by forming heterotetramers with other isoforms which are retained intracellularly and undergo ubiquitin-dependent degradation.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-2963R-A555)
Fornitore: Bioss
Codice articolo fornitore: BS-2963R-A555
Codice articolo locale: BOSSBS-2963R-A555
Descrizione: This gene encodes a member of the superfamily of potassium channel proteins that contain two pore-forming P domains. The encoded protein is an outwardly rectifying channel that is sensitive to changes in extracellular pH and is inhibited by extracellular acidification. Also referred to as an acid-sensitive potassium channel, it is activated by the anesthetics halothane and isoflurane. Although three transcripts are detected in northern blots, there is currently no sequence available to confirm transcript variants for this gene.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11728R-A680)
Fornitore: Bioss
Codice articolo fornitore: BS-11728R-A680
Codice articolo locale: BOSSBS-11728R-A680
Descrizione: 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 Signalling, 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.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11728R)
Fornitore: Bioss
Codice articolo fornitore: BS-11728R
Codice articolo locale: BOSSBS-11728R
Descrizione: 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.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-12173R-A647)
Fornitore: Bioss
Codice articolo fornitore: BS-12173R-A647
Codice articolo locale: BOSSBS-12173R-A647
Descrizione: KCNF1 is a multi-pass membrane-bound protein that acts as an ion channel and is generally expressed as a heterotetramer of potassium channeling proteins. Formerly known as kH1, KCNF1 is usually found as a heteromer with three other potassium channel proteins, KCNG3, KV6.3 and KCNV2. As a potassium channel protein, KCNF1 plays a role in regulating apoptosis and proliferation of pulmonary artery smooth muscle (PASM) cells. Bone morphogenetic proteins (BMPs) restrict proliferation and can induce apoptosis in normal human PASM cells and will upregulate expression of KCNF1 in PASM cells in vitro. KCNF1 is expressed in heart, brain, liver, skeletal muscle, kidney and pancreas.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11728R-HRP)
Fornitore: Bioss
Codice articolo fornitore: BS-11728R-HRP
Codice articolo locale: BOSSBS-11728R-HRP
Descrizione: 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.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11728R-CY5)
Fornitore: Bioss
Codice articolo fornitore: BS-11728R-CY5
Codice articolo locale: BOSSBS-11728R-CY5
Descrizione: 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.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11728R-CY7)
Fornitore: Bioss
Codice articolo fornitore: BS-11728R-CY7
Codice articolo locale: BOSSBS-11728R-CY7
Descrizione: 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.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11728R-A350)
Fornitore: Bioss
Codice articolo fornitore: BS-11728R-A350
Codice articolo locale: BOSSBS-11728R-A350
Descrizione: 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.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11728R-A488)
Fornitore: Bioss
Codice articolo fornitore: BS-11728R-A488
Codice articolo locale: BOSSBS-11728R-A488
Descrizione: 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.
UOM: 1 * 100 µl


Codice catalogo: (87815.290)
Fornitore: VWR Chemicals
Codice articolo locale: VWRC87815.290
Descrizione: Starting materials:
Solution A. Copper sulfate R/ Water R
Solution B. anhydrous Sodium carbonate R / Potassium sodium tartrate R/ Sodium hydrogen carbonate R/ anhydrous Sodium sulfate R/ Water R
UOM: 1 * 1 L

Codice catalogo: (BOSSBS-2963R-CY5.5)
Fornitore: Bioss
Codice articolo fornitore: BS-2963R-CY5.5
Codice articolo locale: BOSSBS-2963R-CY5.5
Descrizione: This gene encodes a member of the superfamily of potassium channel proteins that contain two pore-forming P domains. The encoded protein is an outwardly rectifying channel that is sensitive to changes in extracellular pH and is inhibited by extracellular acidification. Also referred to as an acid-sensitive potassium channel, it is activated by the anesthetics halothane and isoflurane. Although three transcripts are detected in northern blots, there is currently no sequence available to confirm transcript variants for this gene.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-2963R-A750)
Fornitore: Bioss
Codice articolo fornitore: BS-2963R-A750
Codice articolo locale: BOSSBS-2963R-A750
Descrizione: This gene encodes a member of the superfamily of potassium channel proteins that contain two pore-forming P domains. The encoded protein is an outwardly rectifying channel that is sensitive to changes in extracellular pH and is inhibited by extracellular acidification. Also referred to as an acid-sensitive potassium channel, it is activated by the anesthetics halothane and isoflurane. Although three transcripts are detected in northern blots, there is currently no sequence available to confirm transcript variants for this gene.
UOM: 1 * 100 µl


Fornitore: MP Biomedicals
Descrizione: CHOD is soluble in cold 50 mM potassium phosphate buffer, pH 7,0. Prepare solutions immediately before use.

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La disponibilità per questo articolo è limitata, ma potrebbe essere disponibile in un magazzino vicino a voi. Si prega di assicurarsi che si è effettuato l'accesso al sito, in modo che ledisponibilità possano essere visualizzati. Se il call è ancora visualizzato e hai bisogno di assistenza, si prega di telefonare a 1-800-932 - 5000.
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