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  • C8239 - Anti-α-N-Catenin antibody produced in rabbit

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C8239 Sigma-Aldrich

Anti-α-N-Catenin antibody produced in rabbit

IgG fraction of antiserum, buffered aqueous solution

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Properties

Related Categories Alphabetical Index, Antibodies, Antibodies for Cell Biology, Antibodies to Adhesion Molecules and Related Proteins, Antibodies to Cell and Organelle Proteins,
conjugate   unconjugated
clone   polyclonal
biological source   rabbit
application(s)   microarray: suitable
  western blot: 1:1,000 using cytosolic fraction of mouse brain
species reactivity   mouse
mol wt   antigen 102 kDa
form   buffered aqueous solution
shipped in   dry ice
storage temp.   −20°C
antibody form   IgG fraction of antiserum
antibody product type   primary antibodies
UniProt accession no.   Q61301
Gene Information   mouse ... Ctnna2(12386)

Description

General description

The catenins (α, β, γ) are cytoplasmic proteins found in varying developing and adult tissues. α- N-catenin is a cadherin-binding protein, that plays a crucial role in cadherin-mediated cell-cell adhesion. It is widely expressed in the nervous system. α-Catenin (CAP102, 102 kDa), originally described as an E-cadherin associated protein, has been shown to associate with N-cadherin and P-cadherin. Within its conserved region α-catenin shows 30% identity to vinculin. There are at least two subtypes of α-catenin: α-E-catenin and α-N-catenin (102 kDa). The predominant form is α-E-catenin. Alternative spliced forms of α-N-catenin include α-N-catenin I and α-N-catenin II. The ratio of the two isoforms changes during development: isoforms II is more abundant than isoform I in early embryonic development, whereas isoform I is predominant in the adult stage.

Immunogen

synthetic peptide corresponding to a region located near the N-terminus of human α-N-catenin (amino acids 171-186) conjugated to KLH. This sequence is identical in mouse and chicken α-N-catenin. It is not found in α-E-catenin, β-catenin, and γ-catenin.

Application

α-N-Catenin antibody is suitable for microarray and western blot at a dilution of 1:1,000 by using cytosolic fraction of mouse brain.

Physical form

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

Packaging

200 μL in glass insert

Biochem/physiol Actions

Catenins bind directly or indirectly to the conserved cytoplasmic tail domain of the cell adhesion cadherins. The association of catenins to cadherins produces a complex, which is linked to the actin filament network. Catenins/cadherin complexes play an important role in mediating cell adhesion, transduction of cell-cell contact positional signals to the cell interior, and may play a crucial role in cell differentiation. The expression of α-N-catenin is more restricted and this form predominates in the brain and is localized at synaptic junctions.

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
2

Documents

Certificate of Analysis (COA)

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Protocols & Articles

Articles

Antibody Basics

Immunoglobulins (Igs) are produced by B lymphocytes and secreted into plasma. The Ig molecule in monomeric form is a glycoprotein with a molecular weight of approximately 150 kDa that is shaped more ...
Keywords: Affinity chromatography, Centrifugation, Chromatography, Digestions, Direct immunofluorescence, Gene expression, High performance liquid chromatography, Immunofluorescence, Ion Exchange, Microscopy, Precipitation, Purification, Rheumatology, Scanning electron microscopy

Protocols

Western Blot Protocol | Immunoblotting Protocol

Western Blotting refers to the electrophoretic transfer of proteins from sodium dodecyl sulfate polyacrylamide gels to sheets of PVDF or nitrocellullose membrane, followed by immunodetection of prote...
Keywords: AGE, Buffers, Cell disruption, Detection methods, Detergents, Dialysis, Electroblotting, Electrophoresis, Enzyme activity, Gel electrophoresis, Immunoprecipitation, PAGE, Protein extraction, Purification, Sample preparations, Western blot

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Peer-Reviewed Papers
15

References

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