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Masterflex+Single-use+Flow+Sensor
Numéro de catalogue:
(TEST0563.1545)
Fournisseur:
TESTO
Description:
Lux meter testo 545 can measure the illuminance of all common light sources quickly, easily and precisely to ensure productivity, performance and health in workplaces. By automatically calculating the time and point average value, the Lux meter shows all relevant information at a glance.
UOM:
1 * 1 ST
Numéro de catalogue:
(BOSSBS-2436R-A488)
Fournisseur:
Bioss
Description:
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]
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-2436R-A647)
Fournisseur:
Bioss
Description:
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]
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-11421R-FITC)
Fournisseur:
Bioss
Description:
Neuromedin U is a neuropeptide with high activity on smooth muscle. It is widely expressed in gastrointestinal systems and central nervous system (CNS). Peripheral activities of neuromedin U include smooth muscle stimulation, ion transport alterations in the gut and the regulation of local blood flow and adrenocortical function. Neuromedin U receptors 1 and 2 (NMUR1 and NMUR2) are multi-pass membrane proteins that belong to the G-protein coupled receptor 1 family of proteins. Both NMUR1 and NMUR2 act as receptors for the neuromedin U neuropeptide. NMUR1 is detected in peripheral organs, particularly in urogenital and gastrointestinal systems, with highest levels in testis. It’s expression in CNS is low, but the protein has been detected in cerebellum, hippocampus, dorsal root ganglia and spinal cord. NMUR2 is predominantly detected in central nervous system with highest levels detected in medulla oblongata, spinal cord and thalamus. It may also be detected in testis but has low levels of expression in peripheral tissues.
UOM:
1 * 100 µl
Fournisseur:
TESTO
Description:
Sonde de précision, Pénétration, −50...+150 °C, Ø×L: 5×115 mm
Fournisseur:
Lenz Laborglas GmbH & CO.KG
Description:
En verre borosilicaté 3.3 transparent DURAN®.
Fournisseur:
Ludwig Schneider GmbH & CO. KG
Description:
Sonde de température, Class A, −90...+400 °C, Ø×L: 3×400 mm
Numéro de catalogue:
(612-3858)
Fournisseur:
Brand
Description:
Pipette pour usage répétitif, ergonomique et durable, permettant un pipetage intensif rapide et simple et, en association avec la marque PD-Tips (dix tailles différentes de 0,1 µl à 50 ml), elle garantie jusqu'à 49 distributions répétées à partir d'une seule aspiration. Également compatible avec les pointes Combitips®, Combitips® plus et d'autres pointes à usage répétitif standard.
UOM:
1 * 1 ST
Numéro de catalogue:
(TEST0618.0071)
Fournisseur:
TESTO
Description:
Flexible and high-precision for temperature measurements: The digital temperature probe with flexible probe shaft (together with the compatible measuring instrument) is ideal for carrying out measurements in locations that are difficult to access and in liquids.
UOM:
1 * 1 ST
New Product
Numéro de catalogue:
(SENA0096647494951)
Fournisseur:
SenseAnywhere
Description:
The SenseAnywhere AccessPoint is an economic plug and play device that connects SenseAnywhere’s wireless Sensors to the Cloud service of SenseAnywhere.
UOM:
1 * 1 ST
Numéro de catalogue:
(620-0717)
Fournisseur:
TESTO
Description:
Glass pipe for immersion/penetration probe to protect from corrosive agents, for TEST0628.0015
UOM:
1 * 1 ST
Numéro de catalogue:
(BOSSBS-6334R)
Fournisseur:
Bioss
Description:
ORP8 is a member of the oxysterol-binding protein related protein family. In humans, the gene family consists of 12 members, and extensive splice variation increases the number of encoded protein products substantially. The ORPs have been implicated as sterol sensors that regulate a number of cellular functions including sterol and neutral lipid metabolism, intracellular lipid transport, membrane trafficking and cell signaling. ORP8 has been recently shown to act as a sterol sensor that affects the reverse cholesterol transport process via modulation of ABCA1 expression and macrophage cholesterol efflux.
UOM:
1 * 100 µl
Fournisseur:
VWR Collection
Description:
Ces thermomètres numériques mesurent la température des environnements humides ou secs, notamment les congélateurs, réfrigérateurs, bains-marie, aquariums et incubateurs.
Fournisseur:
HELLMA
Description:
Ces cuves sont conçues avec une chambre pour minimiser la formation de bulles.
Numéro de catalogue:
(BOSSBS-15078R-HRP)
Fournisseur:
Bioss
Description:
C1orf85, also known as Lysosomal protein NCU-G1, is a 406 amino acid single-pass membrane protein that is highly glycosylated on its amino-terminal end. Transcription of the gene encoding C1orf85 is activated by TFEB, a transcription factor that specifically recognizes and binds E-box sequences. There are two isoforms of C1orf85 that are produced as a result of alternative splicing events. The C1orf85 maps to human chromosome 1, the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-0836R-A350)
Fournisseur:
Bioss
Description:
Heterodimerizes with PMS2 to form MutL alpha, a component of the post-replicative DNA mismatch repair system (MMR). DNA repair is initiated by MutS alpha (MSH2-MSH6) or MutS beta (MSH2-MSH6) binding to a dsDNA mismatch, then MutL alpha is recruited to the heteroduplex. Assembly of the MutL-MutS-heteroduplex ternary complex in presence of RFC and PCNA is sufficient to activate endonuclease activity of PMS2. It introduces single-strand breaks near the mismatch and thus generates new entry points for the exonuclease EXO1 to degrade the strand containing the mismatch. DNA methylation would prevent cleavage and therefore assure that only the newly mutated DNA strand is going to be corrected. MutL alpha (MLH1-PMS2) interacts physically with the clamp loader subunits of DNA polymerase III, suggesting that it may play a role to recruit the DNA polymerase III to the site of the MMR. Also implicated in DNA damage signaling, a process which induces cell cycle arrest and can lead to apoptosis in case of major DNA damages. Heterodimerizes with MLH3 to form MutL gamma which plays a role in meiosis.
UOM:
1 * 100 µl
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est toujours affiché et vous avez besoin d'aide, s'il vous plaît appelez-nous au 016 385 011
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