Recombinant Phospho-IκB-α (Ser36) Monoclonal Antibody (AN301280L)
 
                        For research use only.
| Verified Samples | Verified Samples in IHC: Human colon | 
| Dilution | IHC 1:500-1:1000 | 
| Isotype | IgG,κ | 
| Host | Rabbit | 
| Reactivity | Human, Mouse, Rat | 
| Applications | IHC | 
| Clonality | Monoclonal;Recombinant | 
| Immunogen | A synthetic peptide corresponding to residues around (Ser36) of Human Phospho-IκB-α | 
| Abbre | IκB-α | 
| Synonyms | EDAID, MAD, IKBA, MAD-3, NFKBI, IKB alpha, NFKBIA, EDAID2, I kappa B alpha, IkappaBalpha, I-kappa-B-alpha, IKBalpha, IkB-alpha, MAD 3, NF kappa B inhibitor alpha, MAD3, alpha, Major histocompatibility complex enhancer-binding protein MAD3, NF-kappa-B inhibitor alpha, Nuclear factor of kappa light chain gene enhancer in B cells, Nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor alpha, nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, pIκBα | 
| Swissprot | |
| Cellular Localization | Cytoplasm, Nucleus, Shuttles between the nucleus and the cytoplasm by a nuclear localization signal (NLS) and a CRM1-dependent nuclear export. | 
| Concentration | 0.2 mg/mL | 
| Buffer | PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant. | 
| Purification Method | Protein A | 
| Research Areas | Signal Transduction, Epigenetics and Nuclear Signaling, Cancer, Immunology | 
| Clone No. | B1043 | 
| Conjugation | Unconjugated | 
| Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. | 
| Shipping | Ice bag | 
| background | This gene encodes a member of the NF-kappa-B inhibitor family, which contain multiple ankrin repeat domains. The encoded protein interacts with REL dimers to inhibit NF-kappa-B/REL complexes which are involved in inflammatory responses. The encoded protein moves between the cytoplasm and the nucleus via a nuclear localization signal and CRM1-mediated nuclear export. Mutations in this gene have been found in ectodermal dysplasia anhidrotic with T-cell immunodeficiency autosomal dominant disease. | 
Other Clones
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Other Formats
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Unconjugated
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