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Recombinant Human CNTN4 Protein, N-His

Catalog #:   YHJ19201 Specific References (50) DATASHEET
Applications: ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Expression system: E. coli
Accession: Q8IWV2
Protein length: Arg731-Asp980
Overview

Catalog No.

YHJ19201

Expression system

E. coli

Species

Homo sapiens (Human)

Protein length

Arg731-Asp980

Predicted molecular weight

30.33 kDa

Nature

Recombinant

Endotoxin level

Please contact with the lab for this information.

Purity

>90% as determined by SDS-PAGE.

Accession

Q8IWV2

Applications

ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress

Form

Lyophilized

Storage buffer

Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.

Reconstitution

Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.

Shipping

In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.

Stability and Storage

Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.

Alternative Names

Contactin-4, BIG-2, Brain-derived immunoglobulin superfamily protein 2, CNTN4

Data Image
  • SDS-PAGE
    SDS PAGE for recombinant Human CNTN4 protein
References

Finding Potential Drug Targets for Pre-Eclampsia Using Mendelian Randomisation and Colocalisation Analysis., PMID:40028697

Identification of Genetic Factors Related With Nonhereditary Colorectal Polyposis and Its Recurrence Through Genome-Wide Association Study., PMID:39629711

Contactin-4 suppresses antitumor T cell responses by engaging amyloid precursor protein., PMID:39392894

Contactin proteins in cerebrospinal fluid show different alterations in dementias., PMID:39317877

Proteomics of left ventricular structure in the Multi-Ethnic Study of Atherosclerosis., PMID:39263947

CNTN4 modulates neural elongation through interplay with APP., PMID:38745463

Whole-genome resequencing of Chinese indigenous sheep provides insight into the genetic basis underlying climate adaptation., PMID:38565986

Potential Schizophrenia Disease-Related Genes Prediction Using Metagraph Representations Based on a Protein-Protein Interaction Keyword Network: Framework Development and Validation., PMID:37966892

Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders., PMID:37120522

MiR-148a-3p attenuates apoptosis and inflammation by targeting CNTN4 in atherosclerosis., PMID:36544657

Value of Immunohistochemical Expression of Apelin, Succinate Dehydrogenase B, Chromogranin B, Human Epidermal Growth Factor Receptor-2, Contactin 4, and Succinyl-CoA Synthetase Subunit Beta in Differentiating Metastatic From Non-Metastatic Pheochromocytoma and Paraganglioma., PMID:35574028

The expression discrepancy and characteristics of long non-coding RNAs in peripheral blood leukocytes from amyotrophic lateral sclerosis patients., PMID:35364800

Members of the vertebrate contactin and amyloid precursor protein families interact through a conserved interface., PMID:34958801

The autism risk gene CNTN4 modulates dendritic spine formation., PMID:34415325

Several Fusion Genes Identified in a Spermatic Cord Leiomyoma With Rearrangements of Chromosome Arms 3p and 21q., PMID:34183386

Multi-omics analysis of genomics, epigenomics and transcriptomics for molecular subtypes and core genes for lung adenocarcinoma., PMID:33750346

Genetic risk score constructed from common genetic variants is associated with cardiovascular disease risk in type 2 diabetes mellitus., PMID:33350037

Exploring the Role of Contactins across Psychological, Psychiatric and Cardiometabolic Traits within UK Biobank., PMID:33182605

Genetic determinants of ammonia-induced acute lung injury in mice., PMID:33050709

Neuronal migration genes and a familial translocation t (3;17): candidate genes implicated in the phenotype., PMID:32028920

Intragenic CNTN4 copy number variants associated with a spectrum of neurobehavioral phenotypes., PMID:31422286

Clinical and Molecular Characterization of Two Patients with CNTN6 Copy Number Variations., PMID:30508811

A Meta-Analysis Including Pre-selected Sequence Variants Associated With Seven Traits in Three French Dairy Cattle Populations., PMID:30459810

Heterogeneity of Cell Surface Glutamate and GABA Receptor Expression in Shank and CNTN4 Autism Mouse Models., PMID:29970989

Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study., PMID:29503163

Genetic variants in PPARGC1B and CNTN4 are associated with thromboxane A2 formation and with cardiovascular event free survival in the Anglo-Scandinavian Cardiac Outcomes Trial (ASCOT)., PMID:29258006

Expression of Contactin 4 Is Associated With Malignant Behavior in Pheochromocytomas and Paragangliomas., PMID:28938490

Nanomechanics of multidomain neuronal cell adhesion protein contactin revealed by single molecule AFM and SMD., PMID:28821864

Investigating the effect of different transducer stiffness values on the contactin complex detachment by steered molecular dynamics., PMID:28651183

Single nucleotide polymorphisms in an Indian cohort and association of CNTN4, MMP2 and SNTB1 variants with oral cancer., PMID:28595731

Constitutional 3p26.3 terminal microdeletion in an adolescent with neuroblastoma., PMID:28402723

A current view on contactin-4, -5, and -6: Implications in neurodevelopmental disorders., PMID:28064060

Body mass index change in gastrointestinal cancer and chronic obstructive pulmonary disease is associated with Dedicator of Cytokinesis 1., PMID:28044437

Psychophysiological endophenotypes to characterize mechanisms of known schizophrenia genetic loci., PMID:27995817

Distortion of the normal function of synaptic cell adhesion molecules by genetic variants as a risk for autism spectrum disorders., PMID:27743928

Investigating the effects of copy number variants on reading and language performance., PMID:27186239

Polymorphism of rs3737597 in DISC1 Gene on Chromosome 1q42.2 in sALS Patients: a Chinese Han Population Case-Control Study., PMID:27052956

GWAS and transcriptional analysis prioritize ITPR1 and CNTN4 for a serum uric acid 3p26 QTL in Mexican Americans., PMID:27039371

Combined Whole Methylome and Genomewide Association Study Implicates CNTN4 in Alcohol Use., PMID:26146898

Contactin-4 mediates axon-target specificity and functional development of the accessory optic system., PMID:25959733

Single gene microdeletions and microduplication of 3p26.3 in three unrelated families: CNTN6 as a new candidate gene for intellectual disability., PMID:25606055

Neurodevelopmental disorders associated with dosage imbalance of ZBTB20 correlate with the morbidity spectrum of ZBTB20 candidate target genes., PMID:25062845

Gene-rich large deletions are overrepresented in POAG patients of Indian and Caucasian origins., PMID:24764060

Dysregulated expression of lipid storage and membrane dynamics factors in Tia1 knockout mouse nervous tissue., PMID:24659297

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations., PMID:24529757

ChIP-seq analysis of histone H3K9 trimethylation in peripheral blood mononuclear cells of membranous nephropathy patients., PMID:24345872

Genetic factors associated with gemcitabine pharmacokinetics, disposition, and toxicity., PMID:24225399

A genome-wide survey of transgenerational genetic effects in autism., PMID:24204716

Association study of 167 candidate genes for schizophrenia selected by a multi-domain evidence-based prioritization algorithm and neurodevelopmental hypothesis., PMID:23922650

Sphingosine-1-phosphate can promote mast cell hyper-reactivity through regulation of contactin-4 expression., PMID:23904439

Datasheet
$ 313
Product specifications
100 μg 313 1 mg 1629

Contact Information

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For research use only. Not for human or drug use.

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Recombinant Human CNTN4 Protein, N-His [YHJ19201]
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