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Choisissez des Panels configurables & des Kits préconfigurés - OU - des MAPmate™ de signalisation cellulaire
Concevez vos kits MILLIPLEX® MAP et obtenez leur prix.
Panels configurables & Kits préconfigurés
Notre large gamme est constituée de panels multiplex qui vous permettent de choisir, au sein d'un panel, les analytes qui répondent le mieux à vos besoins. Sur un autre onglet, vous pouvez choisir un format cytokine préconfiguré ou un kit Simplex.
Kits de signalisation cellulaire & MAPmate™
Choisissez des kits préconfigurés qui permettent d'explorer l'ensemble des voies ou des processus. Ou concevez vos propres kits en choisissant des Simplex MAPmate™ et en suivant les instructions fournies.
Les MAPmate™ suivants ne peuvent pas être utilisés ensemble : -des MAPmate™ qui nécessitent des tampons différents -des paires de MAPmate™ totaux et phospho-spécifiques, par ex. GSK3β total et GSK3β (Ser 9) -des MAPmate™ PanTyr et spécifiques d'un site, par ex. Récepteur Phospho-EGF et phospho-STAT1 (Tyr701) -Plus d'un phospho-MAPmate™ pour une seule cible (Akt, STAT3). -GAPDH et β-Tubuline ne peuvent pas être utilisés avec les kits ou les MAPmate™ contenant panTyr.
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Sélectionner une espèce, un type de panel, un kit ou un type d'échantillon
Pour commencer à concevoir votre kit MILLIPLEX® MAP, sélectionnez une espèce, un type de panel ou un kit d'intérêt.
Custom Premix Selecting "Custom Premix" option means that all of the beads you have chosen will be premixed in manufacturing before the kit is sent to you.
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96-Well Plate
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Ajouter des réactifs supplémentaires (Un kit "Buffer and Detection Kit" est nécessaire pour une utilisation avec les MAPmate™)
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48-602MAG
Buffer Detection Kit for Magnetic Beads
1 Kit
Option de gain de place Nos clients qui commandent plusieurs kits peuvent choisir d'économiser de l'espace de stockage en éliminant l'emballage de chaque kit et de recevoir les composants de leur essai multiplex conditionnés sous poches en plastique pour un stockage plus compact.
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Vous pouvez maintenant concevoir un autre kit personnalisé, choisir un kit pré-configuré, régler vos achats ou fermer l'outil de commande.
Attention: We have moved. Merck Millipore products are no longer available for purchase on MerckMillipore.com.Learn More
Flow refers to the time it takes for a particular flow stream to pass through the filter. The flow rate of a filter is important in determining how rapidly filtration can be completed. Although flow rate generally decreases with pore size among membranes of a single type, membranes with the same pore rating, but made from different materials or by different methods, can have very different flow rates. Flow rate differences can be caused by differences in thickness, porosity, and pore architecture.
After a microporous membrane is produced, flow rate or flow time is measured using an ideal liquid or gas. Hydrophilic filters are usually tested with water. Hydrophobic membranes are usually tested with an alcohol. Membranes to be used for air filtration can be tested with dry air or dry nitrogen. By using ideal liquids and gases, the flow properties of the filter can be assessed independently of particulates or other contaminants that could clog the pores. If there is nothing in the sample stream to clog the pores, the flow rate should remain constant. For ultrafiltration, there are special considerations on flow rate.
Flow Rate and Ultrafiltration
During ultrafiltration, it is important to balance flow rate with retention to obtain optimal performance. With ultrafiltration membranes the term more commonly used is flux. A membrane’s flux is defined as flow divided by the membrane area. The reason that flux is used with ultrafiltration membranes is the need for scalability. Ultrafiltration membranes are commonly used in the purification of expensive biomolecules. Separations are investigated on a small scale in the laboratory before being scaled up to larger volumes in a production setting. Characterizing separations on the basis of flux makes is easier to convert a lab scale investigation to a production scale process.
Using membranes with higher NMWL ratings will increase the flow rate, but at the same time lower the retention. A membrane should be selected for the required retention, coupled with the desired flow rate. This is determined by:
Surface area
Macrosolute type
Solubility
Concentration and diffusivity
Membrane type
Temperature effects on viscosity
Pressure
When concentration polarization is rate-controlling, flux is affected by solute concentration, fluid velocity, flow channel dimensions, and temperature.
Air and Gases
Since sterility is a common requirement of vent membranes, pore rating is an important consideration. Please note that the mechanism of bacterial retention by hydrophobic membranes in a gas stream differs from that for hydrophilic membranes. Bacteria and other pathogens float in air attached to particles (aerosol or dust). Consequently, in air filtration, pathogens can be rejected by membranes with pore sizes larger than the pathogen alone. Membranes with pore sizes up to 5.0 µm are claimed to exhibit >99.99% bacterial retention efficiency by some suppliers. Similar claims exist for viral retention on 0.2 µm membranes. Therefore, membranes with larger pore sizes are used in less critical applications, yielding the benefits of higher flow rate.
When comparing the air flow rates of different membranes, it is important to note the units in which flow rate is reported and any differences in the conditions under which testing was done. Small changes in pressure and temperature can dramatically affect reported air flow rates.
Liquid
Liquid flow is measured by placing the filter into an appropriate holder, adding a defined volume of liquid to the holder, and then pulling the liquid through the filter with a constant vacuum. Flow thus depends on the nature of the liquid, the surface area of the membrane, and the vacuum level. To compare different membranes, the same liquid and vacuum level should be used.
While water and alcohols can be used to test flow rate in large scale testing, they may not provide enough discrimination in predicting membrane performance when a more complex solution such as serum or cell culture medium is to be processed. For specific applications, it is appropriate to use other test solutions. Since complex solutions, such as cell culture media, are considerably more expensive than water or alcohols, sampling plans and test protocols should balance the amount of extra data required against the additional cost.