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.
If you have chosen panel analytes and then choose a premix or single plex kit, you will lose that customization.
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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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Fibronectin, Bovine Plasma Certificates of Analysis
Title
Lot Number
341631
Data Sheet
Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.
Revision
08-December-2010 RFH
Description
Native fibronectin purified from pooled bovine plasma. Effective agent for promoting attachment of cells to commonly-used culture substrates.
Form
Liquid
Formulation
In 150 mM NaCl, 20 mM sodium phosphate buffer, pH 7.3.
Concentration Label
Please refer to vial label for lot-specific concentration
Recommended reaction conditions
Protocol for Coating of Tissue Culture Plates with Fibronectin
This protocol is provided only as a guideline; optimal conditions should be determined as needed. This procedure is based on the use of 21 cm2 dishes and 1 mg fibronectin, which is a sufficient quantity to coat 10 dishes at 5 µg/cm2.
1. Thaw the fibronectin by placing the vial in a 37°C water bath until it is completely thawed. Be VERY careful during the thawing process. DO NOT DISTURB OR REMOVE THE VIAL AT ANY TIME DURING THE THAWING PERIOD. If the vial is disturbed or removed prior to complete thawing, the product will gel and be unusable. DO NOT VORTEX. DO NOT SHAKE AFTER THAWING. Mix very gently after thawing.
2. After thawing, bring the solution to a final volume of 20 ml with sterile, serum-free medium that has been pre-heated to 37°C. This yields a fibronectin solution of 50 µg/ml.
3. Add 2 ml to each of 10 tissue culture dishes and swirl gently to completely coat the entrie growth surface.
4. Incubate the dishes at room temperature for ~45 min to permit binding of the fibronectin to the growth surfaces.
5. Tilt each dish and remove the fibronecting using a sterile pipette. Do not permit the pipette tip to disturb the growth surface.
6. Add the cell suspension in medium directly to the fibronectin-coated dishes and incubate under conditions appropriate to the cells.
CAS number
86088-83-7
Purity
single band by SDS-PAGE
Storage
Avoid freeze/thaw
-20°C
Do Not Freeze
Ok to freeze
Special Instructions
Following initial thaw, aliquot and freeze (-20°C).