Overview
- Product nameAnti-ARNT+ARNT2 antibody
- DescriptionRabbit polyclonal to ARNT+ARNT2
- Tested applicationsELISA, IHC-P, WB more details
- Species reactivityReacts with: Human
Predicted to work with: Mouse, Rat, Zebrafish
- Immunogen
KLH conjugated synthetic peptide: KTGTVKKEGQQSSMRCA, corresponding to N terminal amino acids 214-228 of Human ARNT/ARNT2 containing a predicted sumoylation site.
- Positive controlK562 cell line lysate and human breast carcinoma tissue.
Properties
- FormLiquid
- Storage instructionsShipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
- Storage bufferPreservative: 0.09% Sodium Azide
Constituents: PBS -
Concentration information loading... - PurityProtein G purified
- Purification notesab71719 is purified through a protein G column, eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS.
- Clonality Polyclonal
- IsotypeIgG
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Research Areas
Applications
Our Abpromise guarantee covers the use of ab71719 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
| Application | Notes |
|---|---|
| ELISA | |
| IHC-P | |
| WB |
IHC-P: 1/50 - 1/100.
WB: 1/250 - 1/500. Detects a band of approximately 78 kDa and 86kDa
Not yet tested in other applications.
Optimal dilutions/concentrations should be determined by the end user.
Target
- RelevanceThe aryl hydrocarbon (Ah) receptor is involved in the induction of several enzymes that participate in xenobiotic metabolism. The ligand-free, cytosolic form of the Ah receptor is complexed to heat shock protein 90. Binding of ligand, which includes dioxin and polycyclic aromatic hydrocarbons, results in translocation of the ligand-binding subunit only to the nucleus. Induction of enzymes involved in xenobiotic metabolism occurs through binding of the ligand-bound Ah receptor to xenobiotic responsive elements in the promoters of genes for these enzymes. This gene encodes a protein that forms a complex with the ligand-bound Ah receptor, and is required for receptor function. The encoded protein has also been identified as the beta subunit of a heterodimeric transcription factor, hypoxia-inducible factor 1 (HIF1). A t(1;12)(q21;p13) translocation, which results in a TEL-ARNT fusion protein, is associated with leukemia. Sumoylation of ARNT modulates the ability of ARNT to interact with cooperative molecules such as PML, thereby regulating the transcriptional role of ARNT. This exemplifies a crucial role of protein sumoylation in modulating protein-protein interactions.
- Cellular localizationNuclear
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Database links
- Entrez Gene: 9915 Human
- Entrez Gene: 405 Human
- Entrez Gene: 405 Human
- Entrez Gene: 405 Human
- Entrez Gene: 11864 Mouse
- Entrez Gene: 11863 Mouse
- Entrez Gene: 25243 Rat
- Entrez Gene: 25242 Rat
- Entrez Gene: 64277 Zebrafish
- Omim: 606036 Human
- Omim: 126110 Human
- SwissProt: Q9HBZ2 Human
- SwissProt: P27540 Human
- SwissProt: P27540 Human
- SwissProt: P27540 Human
- SwissProt: Q61324 Mouse
- SwissProt: P53762 Mouse
- SwissProt: Q78E60 Rat
- SwissProt: P41739 Rat
- SwissProt: Q9DG12 Zebrafish
see all
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Alternative names
- ARNT protein 2 antibodyARNT2 antibodyAryl hydrocarbon receptor nuclear translocator antibody
- Aryl hydrocarbon receptor nuclear translocator 2 antibodyBHLHE2 antibodyDioxin receptor, nuclear translocator antibodyHIF1B antibodyHIF1BETA antibodyTANGO antibody
see all
Anti-ARNT+ARNT2 antibody images
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Anti-ARNT+ARNT2 antibody (ab71719) at 1/250 dilution + K562 cell line lysate at 12.5 µg
Predicted band size : 78 kDa
Observed band size : 78 kDa
Additional bands at : 65 kDa. We are unsure as to the identity of these extra bands. -
ab71719, at 1/50 dilution, staining ARNT2 in formalin fixed, paraffin embedded human breast carcinoma tissue by Immunohistochemistry. ab71719 was peroxidase conjugated to the secondary antibody, followed by DAB staining
References for Anti-ARNT+ARNT2 antibody (ab71719)
ab71719 has not yet been referenced specifically in any publications.



