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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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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This Anti-Tie1, C-Terminal Rabbit pAb is validated for use in ELISA, Immunoblotting, Immunofluorescence, Immunohistochemistry for the detection of Tie1, C-Terminal.
More>>This Anti-Tie1, C-Terminal Rabbit pAb is validated for use in ELISA, Immunoblotting, Immunofluorescence, Immunohistochemistry for the detection of Tie1, C-Terminal. Less<<
Anti-Tie1, C-Terminal Rabbit pAb MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.
Anti-Tie1, C-Terminal Rabbit pAb Certificates of Analysis
Title
Lot Number
610200
References
Reference overview
Korhoene, J., et al. 1995. Blood 86, 1828. Iwama, A., et al. 1993. Biochem. Biophys. Res. Commun. 195, 301. Sato, T.N., et al. 1993. Proc. Natl. Acad. Sci. USA 90, 12056. deVries, C., et al. 1992. Science 255, 989. Partenen, J., et al. 1992. Mol. Cell Biol. 12, 1698.
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
07-July-2008 JSW
Synonyms
Anti-Tunica Internal Endothelial Cell Kinase, Anti-Tyrosine Protein Kinase Receptor
A family of receptor tyrosine kinases, TIE1 and TIE2, have been identified in vascular endothelium and hematopoietic cells. TIEs may represent the earliest endothelial cell lineage marker and may regulate the endothelial cell proliferation, differentiation, and proper patterning during vasculogenesis. Tie-1 is a type 1 membrane receptor protein specifically expressed in developing vascular endothelial cells. The extracellular portion of Tie-1 (amino acid residues 25-279) contains 3 fibronectin type III-like, 2 Ig-like C2-type, and 3 EGF-like domains.
Host
Rabbit
Immunogen species
Human
Immunogen
a synthetic peptide corresponding to a amino acids at the C-terminus of human Tie1
Isotype
IgG
Species
bovine, human, mouse, rat
Form
Liquid
Formulation
In PBS, 0.1% BSA, pH 7.4.
Concentration Label
Please refer to vial label for lot-specific concentration
Preservative
None
Comments
Variables associated with assay conditions will dictate the optimal working dilution.
Storage
Avoid freeze/thaw -20°C
Do Not Freeze
Ok to freeze
Special Instructions
Following initial thaw, aliquot and freeze (-20°C).
Toxicity
Standard Handling
References
Korhoene, J., et al. 1995. Blood 86, 1828. Iwama, A., et al. 1993. Biochem. Biophys. Res. Commun. 195, 301. Sato, T.N., et al. 1993. Proc. Natl. Acad. Sci. USA 90, 12056. deVries, C., et al. 1992. Science 255, 989. Partenen, J., et al. 1992. Mol. Cell Biol. 12, 1698.
