RXRB Antibody (Hinge Peptide)
Mouse Monoclonal Antibody
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application
| WB, IHC-P |
---|---|
Primary Accession | P28702 |
Reactivity | Human, Mouse, Rat |
Host | Mouse |
Clonality | Monoclonal |
Calculated MW | 57kDa |
Dilution | IHC-P (1:50), WB (1:1000), |
Gene ID | 6257 |
---|---|
Other Names | Retinoic acid receptor RXR-beta, Nuclear receptor subfamily 2 group B member 2, Retinoid X receptor beta, RXRB, NR2B2 |
Target/Specificity | Specific for the ~48k RXR-0 protein |
Reconstitution & Storage | Long term: -20°C; Short term: +4°C; Avoid freeze-thaw cycles. |
Precautions | RXRB Antibody (Hinge Peptide) is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | RXRB |
---|---|
Synonyms | NR2B2 |
Function | Receptor for retinoic acid. Retinoic acid receptors bind as heterodimers to their target response elements in response to their ligands, all-trans or 9-cis retinoic acid, and regulate gene expression in various biological processes. The RAR/RXR heterodimers bind to the retinoic acid response elements (RARE). |
Cellular Location | Nucleus. Cytoplasm |
Tissue Location | Expressed in aortic endothelial cells (at protein level) (PubMed:28167758). Expressed in monocytes (PubMed:26463675) Expressed in a variety of tumor cell lines |
Volume | 50 µl |
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Provided below are standard protocols that you may find useful for product applications.
Background
Receptor for retinoic acid. Retinoic acid receptors bind as heterodimers to their target response elements in response to their ligands, all-trans or 9-cis retinoic acid, and regulate gene expression in various biological processes. The RAR/RXR heterodimers bind to the retinoic acid response elements (RARE) composed of tandem 5'-AGGTCA-3' sites known as DR1-DR5 (By similarity). Specifically binds 9-cis retinoic acid (9C-RA).
References
Leid M.,et al.Cell 68:377-395(1992).
Leid M.,et al.Cell 71:887-887(1992).
Fleischhauer K.,et al.Nucleic Acids Res. 20:1801-1801(1992).
Numasawa T.,et al.Submitted (MAY-1998) to the EMBL/GenBank/DDBJ databases.
Kaighin V.A.,et al.Submitted (DEC-2010) to the EMBL/GenBank/DDBJ databases.
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