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Recombinant Mouse Contactin-4 Protein, CF

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Product Details

Summary
Reactivity MuSpecies Glossary
Applications Bioactivity
Format
Carrier-Free

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Recombinant Mouse Contactin-4 Protein, CF Summary

Details of Functionality
Measured by its ability to enhance neurite outgrowth of E16-E18 rat embryonic cortical neurons. Immobilized Recombinant Mouse Contactin-4 (as a 3 μL droplet containing 100 ng) on a nitrocellulose coated microplate is sufficient to significantly enhance neurite outgrowth.
Source
Chinese Hamster Ovary cell line, CHO-derived mouse Contactin-4 protein
Asp19-Gly999 (Ile64Leu), with a C-terminal 6-His tag
Accession #
N-terminal Sequence
Asp19
Protein/Peptide Type
Recombinant Proteins
Purity
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Endotoxin Note
<0.01 EU per 1 μg of the protein by the LAL method.

Applications/Dilutions

Dilutions
  • Bioactivity
Theoretical MW
109.5 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
135-155 kDa, reducing conditions

Packaging, Storage & Formulations

Storage
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
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Reconstitution Instructions
Reconstitute at 300 μg/mL in PBS.

Notes

This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.

Alternate Names for Recombinant Mouse Contactin-4 Protein, CF

  • AXCAM
  • axonal-associated cell adhesion molecule
  • BIG-2
  • BIG-2Brain-derived immunoglobulin superfamily protein 2
  • CNTN4
  • contactin 4
  • Contactin4
  • Contactin-4
  • MGC33615
  • neural cell adhesion protein BIG-2

Background

Contactin-4 (CNTN4), also known as BIG-2 (brain-derived immunoglobulin superfamily molecule 2), is an axonal cell adhesion molecule (AxCAM) that belongs to the contactin family, a subfamily of the Ig superfamily (1, 2). The contactin family comprises six members (CNTN1/F3, CNTN2/TAG-1, CNTN3/BIG-1, CNTN4/BIG-2, CNTN5/NB-2 and CNTN6/NB-3) that are characterized by the presence of six Ig like domains, four fibronectin type III-like repeats, and a glycosylphosphatidylinositol (GPI)-anchoring domain (1-4). Contactins are membrane-anchored proteins that can be released as soluble proteins by GPI-specific phospholipase D and are able to promote neurite outgrowth in their soluble form (2). Potential 1026, 705, and 498 amino acid (aa) isoforms of mouse CNTN4 have been described (1, 5). Only the longest isoform includes the C-terminal GPI anchoring sequence. It shares 97% aa identity with rat and 95% aa identity with human, equine and bovine CNTN4 in its mature 981 aa form. It also shares 42-64% aa identity with other CNTN family members, showing highest identity with CNTN3. CNTN4 is expressed throughout the brain, but minor amounts are also detected in small intestine, thyroid, uterus and testis (2, 4). Family members display overlapping but distinct expression patterns in rat brain and are suggested to influence the formation and maintenance of specific neuronal networks (2). In the olfactory bulb, CNTN4 is expressed in specific sensory neurons in a mosaic pattern that is closely correlated with odorant receptor choice, and is thought important for odor mapping (6, 7). In humans, disruption of CNTN4 has been implicated in the 3p deletion syndrome characterized by developmental and growth delay, and in autism spectrum disorder (8-10).

  1. Mimmack, M. L. et al. (1997) Brain Res. Mol. Brain Res. 47:345.
  2. Yoshihara, Y. et al. (1995) J. Neurobiol. 28:51.
  3. Ogawa, J. et al. (1996) Neurosci. Lett. 218:173.
  4. Hansford, L.M. et al. (2003) Cytogenet. Genome Res. 101:17.
  5. Swissprot Accession #Q69Z26.
  6. Saito, H. et al. (1998) Brain Res. Dev. Brain Res. 110:69.
  7. Kaneko-Goto, T. et al. (2008) Neuron 57:834.
  8. Fernandez, T. et al. (2004) Am. J. Hum. Genet. 74:1286.
  9. Fernandez, T. et al. (2008) Am. J. Hum. Genet. 146A:2746.
  10. Roohi, J. et al. (2008) J. Med Genet. doi:10.1136/jmg.2008.057505.

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