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1-Cyclopropyl-4-piperidinone
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1-Cyclopropyl-4-piperidinone
Artikel-Nr:
(BOSSBS-12177R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12177R-CY3
Lokale Artikelnummer::
BOSSBS-12177R-CY3
Beschreibung:
Voltage-gated K+ channels in the plasma membrane are important regulators of electrical signaling, controlling the repolarization and the frequency of action potentials in neurons, muscles and other excitable cells. KCNT2 is a 1,135 amino acid multi-pass transmembrane protein belonging to the potassium channel family (calcium-activated subfamily) of proteins. KCNT2 produces rapidly activating outward rectifier potassium currents in reponse to high intracellular sodium and chloride levels. Its channel activity is inhibited by ATP, inhalation anesthetics, such as isoflourane, and upon stimulation of G-protein coupled receptors, such as mAChR M1 and GluR-1. There are four isoforms of KCNT2 that are produced as a result of alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5875R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5875R-A488
Lokale Artikelnummer::
BOSSBS-5875R-A488
Beschreibung:
Protease. May regulate the surface expression of some potassium channels by retaining them in the endoplasmic reticulum (By similarity).
VE:
1 * 100 µl
Artikel-Nr:
(MMMAH540AV)
Lieferant:
3M
Hersteller-Artikelnummer::
H540AV
Lokale Artikelnummer::
MMMAH540AV
Beschreibung:
Die Kapselgehörschützer sind speziell für starke Lärmbelastung konzipiert und vereinen effektiven Schutz mit höchstem Tragekomfort. Das Modell H540AV mit Kopfband ist im Hi-VIZ-Design für hohe Sichtbarkeit. Der Vorteil wie Gespräche und Warnsignale sind dennoch gut verständlich. Durch eine akustische Verbindung zwischen dem Kapselinnenraum und dem Schalenzwischenraum wird zudem eine optimale Niederfrequenzdämmung erreicht.
VE:
1 * 1 ST
Artikel-Nr:
(87764.180)
Lieferant:
VWR Chemicals
Lokale Artikelnummer::
VWRC87764.180
Beschreibung:
Aluminiumchlorid Reag. Ph. Eur. 1002701
VE:
1 * 100 mL
Artikel-Nr:
(BOSSBS-13192R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13192R-CY3
Lokale Artikelnummer::
BOSSBS-13192R-CY3
Beschreibung:
Fibronectins are multi-domain glycoproteins that bind to a variety of substances including collagen, actin, heparin, DNA, fibrin and fibronectin receptors. They are involved in a diverse array of important functions such as blood coagulation, wound healing, cell adhesion, cell differentiation and migration. FNDC4 (Fibronectin type III domain-containing protein 4), also known as FRCP1 (Fibronectin type III repeat-containing protein 1), is a 234 amino acid membrane protein that contains one fibronectin type-III domain, which serves as a binding site for DNA, heparin or the cell surface. The gene encoding FNDC4 is localized to human chromosome two, which houses over 1,400 genes and comprises nearly 8% of the human genome.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13192R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13192R
Lokale Artikelnummer::
BOSSBS-13192R
Beschreibung:
Fibronectins are multi-domain glycoproteins that bind to a variety of substances including collagen, actin, heparin, DNA, fibrin and fibronectin receptors. They are involved in a diverse array of important functions such as blood coagulation, wound healing, cell adhesion, cell differentiation and migration. FNDC4 (Fibronectin type III domain-containing protein 4), also known as FRCP1 (Fibronectin type III repeat-containing protein 1), is a 234 amino acid membrane protein that contains one fibronectin type-III domain, which serves as a binding site for DNA, heparin or the cell surface. The gene encoding FNDC4 is localized to human chromosome two, which houses over 1,400 genes and comprises nearly 8% of the human genome.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-2436R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2436R-CY5.5
Lokale Artikelnummer::
BOSSBS-2436R-CY5.5
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. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins and is found associated with the sulfonylurea receptor SUR. Mutations in this gene are a cause of familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder characterized by unregulated insulin secretion. Defects in this gene may also contribute to autosomal dominant non-insulin-dependent diabetes mellitus type II (NIDDM), transient neonatal diabetes mellitus type 3 (TNDM3), and permanent neonatal diabetes mellitus (PNDM). Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq]
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-2436R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2436R-CY7
Lokale Artikelnummer::
BOSSBS-2436R-CY7
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. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins and is found associated with the sulfonylurea receptor SUR. Mutations in this gene are a cause of familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder characterized by unregulated insulin secretion. Defects in this gene may also contribute to autosomal dominant non-insulin-dependent diabetes mellitus type II (NIDDM), transient neonatal diabetes mellitus type 3 (TNDM3), and permanent neonatal diabetes mellitus (PNDM). Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq]
VE:
1 * 100 µl
Artikel-Nr:
(84750.600)
Lieferant:
VWR Chemicals
Lokale Artikelnummer::
VWRC84750.600
Beschreibung:
Linearitätsstandards in dauerhaft versiegelten UV-Küvetten oder in 100-ml-Braunglasflaschen.
VE:
1 * 1 SET
Lieferant:
Alfa Aesar
Beschreibung:
Natriumhexafluoroaluminat ≥99,5% (Metall-Basis)
Artikel-Nr:
(BOSSBS-1856R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1856R-A350
Lokale Artikelnummer::
BOSSBS-1856R-A350
Beschreibung:
Endopeptidase that degrades various components of the extracellular matrix, such as collagen type III and fibronectin. Activates progelatinase A. Involved in the matrix remodeling of blood vessels. Isoform short cleaves fibronectin and also collagen type III, but at lower rate. It has no effect on type I, II, IV and V collagen. However, upon interaction with CSPG4, it may be involved in degradation and invasion of type I collagen by melanoma cells.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-2436R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2436R-A488
Lokale Artikelnummer::
BOSSBS-2436R-A488
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. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins and is found associated with the sulfonylurea receptor SUR. Mutations in this gene are a cause of familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder characterized by unregulated insulin secretion. Defects in this gene may also contribute to autosomal dominant non-insulin-dependent diabetes mellitus type II (NIDDM), transient neonatal diabetes mellitus type 3 (TNDM3), and permanent neonatal diabetes mellitus (PNDM). Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq]
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-2436R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2436R-A647
Lokale Artikelnummer::
BOSSBS-2436R-A647
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. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins and is found associated with the sulfonylurea receptor SUR. Mutations in this gene are a cause of familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder characterized by unregulated insulin secretion. Defects in this gene may also contribute to autosomal dominant non-insulin-dependent diabetes mellitus type II (NIDDM), transient neonatal diabetes mellitus type 3 (TNDM3), and permanent neonatal diabetes mellitus (PNDM). Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq]
VE:
1 * 100 µl
Artikel-Nr:
(USBI135136)
Lieferant:
US Biological
Hersteller-Artikelnummer::
135136
Lokale Artikelnummer::
USBI135136
Beschreibung:
Anti-UROS Rabbit Polyclonal Antibody
VE:
1 * 100 µG
Artikel-Nr:
(BOSSBS-12181R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12181R-CY3
Lokale Artikelnummer::
BOSSBS-12181R-CY3
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. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins and is found associated with the sulfonylurea receptor SUR. Mutations in this gene are a cause of familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder characterized by unregulated insulin secretion. Defects in this gene may also contribute to autosomal dominant non-insulin-dependent diabetes mellitus type II (NIDDM), transient neonatal diabetes mellitus type 3 (TNDM3), and permanent neonatal diabetes mellitus (PNDM). Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq]
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-3348R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3348R-CY3
Lokale Artikelnummer::
BOSSBS-3348R-CY3
Beschreibung:
PSD 93 is believed to participate in the clustering of certain proteins, including N-methyl-D-aspartate (NMDA) receptors and shaker-type potassium channels at the synaptic membrane. There are two principal modes of interaction between PSD 93 and other proteins. NMDA receptors and shaker-type potassium channels both share C-terminal sequence homology consisting of a threonine/serine-X-valine-COOH (T/SXV) motif. Other neuronal proteins that share this motif (beta 1 adrenergic receptor, some serotonin receptors, some sodium channel subunits, and additional potassium channel subunits) may interact with PSD 93 by binding to its PDZ domains. Neuronal nitric oxide synthase (nNOS), which lacks the T/SXV motif but which has its own PDZ domain, has been shown to associate with PSD 93 in vitro through a pseudo-homotypic PDZ-PDZ interaction.
VE:
1 * 100 µl
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.
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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