Our broad portfolio consists of multiplex panels that allow you to choose, within the panel, analytes that best meet your needs. On a separate tab you can choose the premixed cytokine format or a single plex kit.
Cell Signaling Kits & MAPmates™
Choose fixed kits that allow you to explore entire pathways or processes. Or design your own kits by choosing single plex MAPmates™, following the provided guidelines.
The following MAPmates™ should not be plexed together:
-MAPmates™ that require a different assay buffer
-Phospho-specific and total MAPmate™ pairs, e.g. total GSK3β and GSK3β (Ser 9)
-PanTyr and site-specific MAPmates™, e.g. Phospho-EGF Receptor and phospho-STAT1 (Tyr701)
-More than 1 phospho-MAPmate™ for a single target (Akt, STAT3)
-GAPDH and β-Tubulin cannot be plexed with kits or MAPmates™ containing panTyr
.
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Select A Species, Panel Type, Kit or Sample Type
To begin designing your MILLIPLEX® MAP kit select a species, a panel type or kit of interest.
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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Species
Panel Type
Selected Kit
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96-Well Plate
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Add Additional Reagents (Buffer and Detection Kit is required for use with MAPmates)
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48-602MAG
Buffer Detection Kit for Magnetic Beads
1 Kit
Space Saver Option Customers purchasing multiple kits may choose to save storage space by eliminating the kit packaging and receiving their multiplex assay components in plastic bags for more compact storage.
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Millistak+® HC Pro
Fully synthetic depth filters for clarification and downstream filtration applicationsMore
Fully synthetic depth filters for clarification and downstream filtration applications Less
C190242Fully synthetic depth filters for clarification and downstream filtration applications
Millistak+® HC Pro (high capacity synthetic media) is a family of synthetic depth filters providing a cleaner and more consistent depth filtration media over current diatomaceous earth (DE) and cellulose (CE) based filter offerings. Multiple media grades are available for primary and secondary clarification as well as downstream filtration applications.
Features & Benefits
Synthetic materials of construction
Reduce TOC extractables and pre-use flush volume requirements by 50%
No beta glucans to interfere with limulous amoebocyte lysate (LAL) testing for bacterial endotoxins
Lot to lot consistency for successful development and implementation of robust clarification processes
Depth filter media formulation & design
Provide as much as two times the filtration capacity with equivalent filter retention properties over commercial DE-based benchmarks
Improved HCP impurity clearance
Disposable Pod device
Flexible, modular format offers scalability from 5 to 12,000 liters or more
Robust device format; easy to use and set up
The Emprove® Program
The Emprove® Program complements the product portfolio through
Comprehensive documentation to support qualification, risk assessment and process optimization needs.
Consolidation of product specific testing, quality and regulatory information to simplify compliance requirements.
Convenient 24/7 access to up-to-date product information.
Media Grade
D0SP
C0SP
X0SP
Surface Area
23 cm2
23 cm2
23 cm2
Materials of Construction
Depth Filter Media
Silica Filter Aid with Polyacrylic Fiber
Filter non-woven
Polypropylene
N/A
N/A
Pod Housings
Glass Filled Polypropylene
Inlet, Vent and Outlet Connections
Female Luer
Pod (Device) dimensions
Length
3.5" (8.9 cm)
Height
2.6" (6.6 cm)
Thickness
1.6” (4.1 cm)
Maximum Operating Pressure
50 psid (3.5 bar) @ ≤40°C
Maximum Differential Pressure
Forward
30 psid (2.1 bar) @ 40 °C
Reverse
15 psid (1.0 bar) @ 40 °C
Sterilization
Sterilization 2 cycles of 60 minutes at 123 °C 1 cycle of 60 minutes at 123 °C
Toxicity
All component materials meet the requirements of the current USP <88> biological reactivity test for class VI plastics.
Bacterial Endotoxin
Bacterial Endotoxin < 0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test
Pressure Equipment Directive 2014/68/EU3
Devices and associated holders are designed and manufactured in accordance with the sound engineering practices (SEP) cited in Article 4(3) of 2014/68/EU
