Full Product Name
Chicken CNTN1 Polyclonal Antibody
Product Synonym Names
Neural cell recognition molecule F11
Product Gene Name
anti-CNTN1 antibody
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Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
3D Structure
ModBase 3D Structure for Q12860
Species Reactivity
Human, Mouse, Rat
Purity/Purification
Immunogen Affinity Purified
Form/Format
Liquid; 0.1MxPBS, 50% Glycerol, pH7.5
Concentration
200 ug/ml (lot specific)
Immunogen
Recombinant Human CNTN1 Protein
Preparation and Storage
Store at 4 degree C for frequent use. Store at -20 degree C to -70 degree C for 6 months.
Other Notes
Small volumes of anti-CNTN1 antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Applications Tested/Suitable for anti-CNTN1 antibody
Western Blot (WB), Immunohistochemistry (IHC)
NCBI/Uniprot data below describe general gene information for CNTN1. It may not necessarily be applicable to this product.
NCBI GenBank Nucleotide #
NP_001242993.1
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UniProt Primary Accession #
Q12860
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UniProt Related Accession #
Q12860[Other Products]
NCBI Official Full Name
contactin-1 isoform 3
NCBI Official Synonym Full Names
contactin 1
NCBI Official Symbol
CNTN1 [Similar Products]
NCBI Official Synonym Symbols
F3; GP135; MYPCN
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NCBI Protein Information
contactin-1
UniProt Protein Name
Contactin-1
UniProt Synonym Protein Names
Glycoprotein gp135; Neural cell surface protein F3
UniProt Gene Name
CNTN1 [Similar Products]
UniProt Entry Name
CNTN1_HUMAN
NCBI Summary for CNTN1
The protein encoded by this gene is a member of the immunoglobulin superfamily. It is a glycosylphosphatidylinositol (GPI)-anchored neuronal membrane protein that functions as a cell adhesion molecule. It may play a role in the formation of axon connections in the developing nervous system. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]
UniProt Comments for CNTN1
CNTN1: Contactins mediate cell surface interactions during nervous system development. Involved in the formation of paranodal axo-glial junctions in myelinated peripheral nerves and in the signaling between axons and myelinating glial cells via its association with CNTNAP1. Participates in oligodendrocytes generation by acting as a ligand of NOTCH1. Its association with NOTCH1 promotes NOTCH1 activation through the released notch intracellular domain (NICD) and subsequent translocation to the nucleus. Interaction with TNR induces a repulsion of neurons and an inhibition of neurite outgrowth. Defects in CNTN1 are the cause of Compton-North congenital myopathy (CNCM). CNCM is a familial lethal form of congenital onset muscle weakness, inherited in an autosomal-recessive fashion and characterized by a secondary loss of beta2-syntrophin and alpha-dystrobrevin from the muscle sarcolemma, central nervous system involvement, and fetal akinesia. Belongs to the immunoglobulin superfamily. Contactin family. 3 isoforms of the human protein are produced by alternative splicing.
Protein type: Cell adhesion; Membrane protein, GPI anchor
Chromosomal Location of Human Ortholog: 12q11-q12
Cellular Component: membrane; plasma membrane
Molecular Function: carbohydrate binding; glycoprotein binding
Biological Process: axon guidance; Notch signaling pathway; cerebellum development; cell adhesion
Disease: Myopathy, Congenital, Compton-north
Research Articles on CNTN1
1. Findings suggest that PLP1 and CNTN1 gene variations modulate specific aspects of callosal microstructure that are in line with their gene function.
Precautions
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Disclaimer
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