Product Name
Contactin 1 (CNTN1), ELISA Kit
Full Product Name
Camel Contactin 1 ELISA Kit
Product Gene Name
CNTN1 elisa kit
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Request for Current Manual Insert
Request Current Manual
Chromosome Location
Chromosome: 12; NC_000012.11 (41086244..41466214). Location: 12q11-q12
3D Structure
ModBase 3D Structure for Q12860
Preparation and Storage
Store all reagents at 2-8 degree C
Product Note
Select online data sheet information is drawn from bioinformatics databases, occasionally resulting in ambiguous or non-relevant product information. It is the responsibility of the customer to review, verify, and evaluate the information to make sure it matches their requirements before purchasing the kit. Our ELISA Kit assays are dynamic research tools and sometimes they may be updated and improved. If the format of this assay is important to you then please request the current manual or contact our technical support team with a presales inquiry before placing an order. We will confirm the current details of the assay. We cannot guarantee the sample manual posted online is the most current manual.
Other Notes
Small volumes of CNTN1 elisa kit 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.
Searchable Terms for CNTN1 purchase
MBS098370 is a ready-to-use microwell, strip-or-full plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the Contactin 1 (CNTN1) ELISA Kit target analytes in
biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing CNTN1. The ELISA analytical biochemical technique of the MBS098370 kit is based on CNTN1 antibody-CNTN1 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect CNTN1 antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, CNTN1. Appropriate sample types may include undiluted body fluids and/or tissue homogenates, secretions. Quality control assays assessing reproducibility identified the intra-assay CV (%) and inter-assay CV(%).
NCBI/Uniprot data below describe general gene information for CNTN1. It may not necessarily be applicable to this product.
NCBI Accession #
NP_001242993.1
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NCBI GenBank Nucleotide #
NM_001256064.1
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UniProt Primary Accession #
Q12860
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UniProt Secondary Accession #
Q12861; Q14030; Q7M4P0; Q8N466; A8K0H9; A8K0Y3[Other Products]
UniProt Related Accession #
Q12860[Other Products]
Molecular Weight
113,320 Da
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
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NCBI Protein Information
contactin-1; glycoprotein gP135; neural cell surface protein F3
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: Membrane protein, GPI anchor; Cell adhesion
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. a completely novel function for F3/Contactin - modulator of neurogenesis
Precautions
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.
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