Recombinant Human Contactin-1 Fc Chimera Protein, CF Summary
Details of Functionality
Measured by its binding ability in a functional ELISA. Immobilized Recombinant Human (rh) NrCAM Fc Chimera
(Catalog #
2034-NR)
at 1 μg/mL (100 μL/well) can bind rhContactin-1 Fc Chimera with a linear range of 0.3-20 ng/mL.
Source
Spodoptera frugiperda, Sf 21 (baculovirus)-derived human Contactin-1 protein
Human Contactin-1 (Glu21-Ser993) Accession # CAA79696
>90%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Endotoxin Note
<1.0 EU per 1 μg of the protein by the LAL method.
Applications/Dilutions
Dilutions
Binding Activity2
Bioactivity
Theoretical MW
135 kDa. Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
SDS-PAGE
135-150 kDa, reducing conditions
Publications
Read Publication using 904-CN in the following applications:
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
12 months from date of receipt, -20 to -70 °C as supplied.
1 month, 2 to 8 °C under sterile conditions after reconstitution.
3 months, -20 to -70 °C under sterile conditions after reconstitution.
Buffer
Lyophilized from a 0.2 μm filtered solution in PBS.
Purity
>90%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Reconstitution Instructions
Reconstitute at 100 μg/mL in sterile PBS.
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Human Contactin-1 Fc Chimera Protein, CF
CNTN1
contactin 1
Contactin1
Contactin-1
F11
F3
F3cam
Glycoprotein gp135
GP135
Neural cell surface protein F3
Background
Contactin-1 (CNTN1), also known as F3 and F11, is an approximately 135 kDa GPI-anchored member of the Contactin family of neuronal adhesion glycoproteins (1). Mature human Contactin-1 contains 6 Ig-like domains and 4 fibronectin type III-like domains, and it shares 96% amino acid (aa) sequence identity with mouse and rat Contactin-1 (2, 3). Alternative splicing generates an isoform with an 11 aa deletion N-terminal to the first Ig-like domain and another isoform that is substituted and truncated following the sixth Ig-like domain. A soluble form of Contactin-1 is released into the cerebrospinal fluid (4). Contactin-1 is expressed on neurons and their precursors at sites of glial cell contact with neuronal processes (5-7). Within paranodal regions of the axon, Contactin-1 associates in cis with the transmembrane protein Caspr (7). It binds in trans to other neuronal adhesion proteins (e.g. NrCAM, Neurofascin, Tenascin R), the phosphatase PTPRZ, and the chondroitin sulfate CS-E (8-13). It also binds and activates both Notch-1 and Notch-2 (14). Ligation of Contactin-1 promotes neurite outgrowth, adhesion to Schwann cells, axon myelination, and differentiation of oligodendrocytes and cerebellar granule neurons, but it can also negatively regulate neurogenesis in the ventricular zone (4, 6-9, 12-14). In cancer, Contactin-1 is up-regulated by VEGF-C and is required for VEGF R3/Flt-4 induced tumor cell invasion and metastasis (15).
Shimoda, Y. and K. Watanabe (2009) Cell Adh. Migr. 3:64.
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