Human/Mouse/Rat Contactin-2/TAG1 Antibody Summary
Leu29-Asn1012
Accession # Q02246
Applications
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Scientific Data
Detection of Human, Mouse, and Rat Contactin‑2/TAG1 by Western Blot. Western blot shows lysates of human cerebellum tissue, mouse brain tissue, and rat brain tissue. PVDF membrane was probed with 1 µg/mL of Goat Anti-Human/Mouse/Rat Contactin-2/TAG1 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF1714) followed by HRP-conjugated Anti-Goat IgG Secondary Antibody (Catalog # HAF017). A specific band was detected for Contactin-2/TAG1 at approximately 135 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.
Contactin‑2/TAG1 in Human Brain. Contactin-2/TAG1 was detected in immersion fixed paraffin-embedded sections of human brain (cortex) using Goat Anti-Human/Mouse/Rat Contactin-2/TAG1 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF1714) at 15 µg/mL overnight at 4 °C. Tissue was stained using the Anti-Goat HRP-DAB Cell & Tissue Staining Kit (brown; Catalog # CTS008) and counterstained with hematoxylin (blue). Specific staining was localized to neuronal processes. View our protocol for Chromogenic IHC Staining of Paraffin-embedded Tissue Sections.
Detection of Human Contactin‑2/TAG1 by Simple WesternTM. Simple Western lane view shows lysates of human brain (cerebellum and hippocampus), loaded at 0.2 mg/mL. A specific band was detected for Contactin‑2/TAG1 at approximately 160 kDa (as indicated) using 20 µg/mL of Goat Anti-Human/Mouse/Rat Contactin‑2/TAG1 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF1714). This experiment was conducted under reducing conditions and using the 12-230 kDa separation system.
Reconstitution Calculator
Preparation and Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Background: Contactin-2/TAG1
Contactin-2 (CNTN2), also called TAG-1 (transient axonal glycoprotein), TAX1 (transiently-expressed axonal glycoprotein), or axonin-1, is a 135 kDa glycosyl‑phosphatidylinositol (GPI)- anchored cell adhesion molecule that belongs to the contactin subfamily within the immunoglobulin (Ig) protein superfamily (1‑3). Human Contactin-2 cDNA encodes a 28 amino acid (aa) signal peptide, a 984 aa mature secreted protein with six Ig-like domains followed by four fibronectin type III‑like repeats, and a 28 aa C-terminal GPI anchor pro-sequence. GPI-specific phospholipase activity can release soluble, active Contactin-2 from the membrane (2). Mature human Contactin-2 shares approximately 93%, 93% and 75% aa sequence identity with human, rat and chicken Contactin-2, respectively. During development, Contactin-2 is expressed by a subset of neuronal populations in the central nervous system (CNS) and peripheral nervous system (PNS), particularly during initial phases of axon outgrowth (3‑5). Both the 135 kDa form and a 90 kDa form are also upregulated in response to CNS injury in the adult (6). Data support a role for Contactin-2 in axon pathfinding, neurite outgrowth and adhesion, especially in the CNS (3‑6). In mature myelinated fibers, Contactin‑2 is expressed by oligodendrocytes and Schwann cells, which are myelinating glial cells of the CNS and PNS, respectively (7, 8). It is enriched in the juxtaparanodal regions, where it recruits caspr2 (Contactin‑associated protein 2), a transmembrane neurexin involved in cell adhesion and intercellular communication (7‑10). The axonal Contactin‑2 interacts in cis with caspr2, and in trans with another Contactin‑2 on the glial membrane (8). This ternary complex is required for the accumulation and organization of K+ channels in the juxtaparanodes (9).
- Wolfer, D. & R. J. Giger (1994) Swissprot Accession # Q61330.
- Hasler, T.H. et al. (1993) Eur. J. Biochem. 211:329.
- Karagogeos, D. (2003) Front. Biosci.8:s1304.
- Liu, Y. & M.C. Halloran (2005) J. Neurosci. 25:10556.
- Denaxa, M. et al. (2005) Dev. Biol. 288:87.
- Soares, S. et al. (2005) Eur. J. Neurosci. 21:1169.
- Traka, M. et al. (2002) J. Neurosci. 22:3016.
- Poliak, S. and E. Peles (2003) Nature Reviews Neurosci. 4:968.
- Traka, M. et al. (2003) J. Cell Biol. 162:1161.
- Poliak, S. et al. (2003) J. Cell Biol. 162:1149.
Product Datasheets
Citations for Human/Mouse/Rat Contactin-2/TAG1 Antibody
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
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Citations: Showing 1 - 10
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Nkx2-5 Loss of Function in the His-Purkinje System Hampers Its Maturation and Leads to Mechanical Dysfunction
Authors: Choquet, C;Sicard, P;Vahdat, J;Nguyen, THM;Kober, F;Varlet, I;Bernard, M;Richard, S;Kelly, RG;Lalev�e, N;Miquerol, L;
Journal of cardiovascular development and disease
Species: Mouse
Sample Types: Whole Tissue
Applications: IHC -
p75NTR prevents the onset of cerebellar granule cell migration via RhoA activation
Authors: Juan P Zanin, Wilma J Friedman
eLife
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The m6 A Readers YTHDF1 and YTHDF2 Synergistically Control Cerebellar Parallel Fiber Growth by Regulating Local Translation of the Key Wnt5a Signaling Components in Axons
Authors: Jun Yu, Yuanchu She, Lixin Yang, Mengru Zhuang, Peng Han, Jianhui Liu et al.
Advanced Science
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Nkx2-5 defines distinct scaffold and recruitment phases during formation of the murine cardiac Purkinje fiber network
Authors: C Choquet, RG Kelly, L Miquerol
Nat Commun, 2020-10-20;11(1):5300.
Species: Mouse
Sample Types: Whole Tissue
Applications: IHC -
Dorsal-to-Ventral Cortical Expansion Is Physically Primed by Ventral Streaming of Early Embryonic Preplate Neurons
Authors: K Saito, M Okamoto, Y Watanabe, N Noguchi, A Nagasaka, Y Nishina, T Shinoda, A Sakakibara, T Miyata
Cell Rep, 2019-11-05;29(6):1555-1567.e5.
Species: Mouse
Sample Types: Whole Tissue
Applications: IHC -
Genetic analysis of the organization, development and plasticity of corneal innervation in mice
Authors: N Bouheraoua, S Fouquet, M Teresa Mar, D Karagogeos, L Laroche, A Chédotal
J. Neurosci., 2018-12-26;0(0):.
Species: Transgenic Mouse
Sample Types: Whole Embryo
Applications: IHC -
Deletion of Nkx2-5 in trabecular myocardium reveals the developmental origins of pathological heterogeneity associated with ventricular non-compaction cardiomyopathy
Authors: C Choquet, THM Nguyen, P Sicard, E Buttigieg, TT Tran, F Kober, I Varlet, R Sturny, MW Costa, RP Harvey, C Nguyen, P Rihet, S Richard, M Bernard, RG Kelly, N Lalevée, L Miquerol
PLoS Genet., 2018-07-06;14(7):e1007502.
Species: Mouse
Sample Types: Whole Tissue
Applications: IHC -
hPSC Modeling Reveals that Fate Selection of Cortical Deep Projection Neurons Occurs in the Subplate
Authors: MZ Ozair, C Kirst, BL van den Be, A Ruzo, T Rito, AH Brivanlou
Cell Stem Cell, 2018-06-21;0(0):.
Species: Human
Sample Types: Whole Tissue
Applications: IHC -
Segregation of Central Ventricular Conduction System Lineages in Early SMA+ Cardiomyocytes Occurs Prior to Heart Tube Formation
Authors: Caroline Choquet, Laetitia Marcadet, Sabrina Beyer, Robert G. Kelly, Lucile Miquerol
Journal of Cardiovascular Development and Disease
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Floor plate-derived neuropilin-2 functions as a secreted semaphorin sink to facilitate commissural axon midline crossing
Authors: Berenice Hernandez-Enriquez, Zhuhao Wu, Edward Martinez, Olav Olsen, Zaven Kaprielian, Patricia F. Maness et al.
Genes & Development
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Lewis(x) and alpha2,3-sialyl glycans and their receptors TAG-1, Contactin, and L1 mediate CD24-dependent neurite outgrowth.
Authors: Lieberoth A, Splittstoesser F, Katagihallimath N, Jakovcevski I, Loers G, Ranscht B, Karagogeos D, Schachner M, Kleene R
J. Neurosci., 2009-05-20;29(20):6677-90.
Species: Mouse
Sample Types: Tissue Homogenates, Whole Cells
Applications: ICC, Immunoprecipitation, Neutralization
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