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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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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Description
Overview
Hydrolyzes β1,4-glucan linkages in cellulose. Has been used to isolate intact cells and protoplasts from plant tissues.
Note: 1 KU = 1000 units.
Catalogue Number
219466
Brand Family
Calbiochem®
References
References
Takebe, I., et al. 1968. Plant Cell Physiol.9, 115. Tomita, Y., et al. 1968. J. Ferment. Technol.46, 701.
Product Information
CAS number
9012-54-8
Activity
≥10,000 units/g dry weight.
Unit of Definition
One unit is a measure of decomposing activity using a filter paper substrate at 40°C, pH 4.0.
EC number
3.2.1.4
Form
Yellowish white solid
Applications
Biological Information
Physicochemical Information
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
R Phrase
R: 42
May cause sensitization by inhalation.
S Phrase
S: 22-24-36/37
Do not breathe dust. Avoid contact with skin. Wear suitable protective clothing and gloves.
Product Usage Statements
Storage and Shipping Information
Ship Code
Blue Ice Only
Toxicity
Harmful
Storage
+2°C to +8°C
Do not freeze
Ok to freeze
Special Instructions
Following reconstitution, aliquot and freeze (-20°C) for long term storage or refrigerate (4°C) for short term storage. Stock solutions are stable for up to 3 days at 4°C or for up to 1 month at -20°C.
CELLULYSIN® Cellulase, Trichoderma viride Certificates of Analysis
Title
Lot Number
219466
References
Reference overview
Takebe, I., et al. 1968. Plant Cell Physiol.9, 115. Tomita, Y., et al. 1968. J. Ferment. Technol.46, 701.
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
05-June-2008 RFH
Description
Hydrolyzes b1,4-glucan linkages in cellulose. Has been used to isolate intact cells and protoplasts from plant tissues.
Form
Yellowish white solid
CAS number
9012-54-8
EC number
3.2.1.4
Activity
≥10,000 units/g dry weight.
Unit definition
One unit is a measure of decomposing activity using a filter paper substrate at 40°C, pH 4.0.
Solubility
H₂O
Storage
+2°C to +8°C
Do Not Freeze
Ok to freeze
Special Instructions
Following reconstitution, aliquot and freeze (-20°C) for long term storage or refrigerate (4°C) for short term storage. Stock solutions are stable for up to 3 days at 4°C or for up to 1 month at -20°C.
Toxicity
Harmful
References
Takebe, I., et al. 1968. Plant Cell Physiol.9, 115. Tomita, Y., et al. 1968. J. Ferment. Technol.46, 701.
