| 产品详情 |
| Edit |   |
| Antigenic Specificity | Programmed Cell Death 4 (Neoplastic Transformation Inhibitor) (PDCD4) (Ser457), (phosphorylated) |
| Clone | polyclonal |
| Host Species | Rabbit |
| Reactive Species | human, mouse, rat, Xenopus laevis |
| Isotype | n/a |
| Format | unconjugated |
| Size | 25 µL |
| Concentration | n/a |
| Applications | ELISA,Immunohistochemistry (IHC),Western Blotting (WB) |
| Reviews / Ratings | If you have used this antibody, please help fellow researchers by submitting reviews to pAbmAbs and antYbuddY. |
| Description | Pdcd4 pS457 is suitable for Cancer, Immunology and Nuclear Signaling research. Programmed cell death 4 (Pdcd4) is a novel tumor supressor. Pdcd4 directly inhibits the helicase activity of eukaryotic translation initiation factor 4A (eIF4A), a component of the translation initiation complex. Pdcd4 also suppresses the transactivation of activator protein-1 (AP-1)-responsive promoters by c-Jun. Pdcd4 contains two Akt phosphorylation sites, one at Ser67 and the other at Ser457. The phosphorylation of Pdcd4 by Akt causes nuclear translocation of Pdcd4 and a significant decrease in the ability of Pdcd4 to interfere with the transactivation of AP-1-responsive promoters by c-Jun. Synonyms: Death up-regulated gene protein antibody, Dug antibody, H731 antibody, Ma3 antibody, Neoplastic transformation inhibitor antibody, Neoplastic transformation inhibitor protein antibody, Nuclear antigen H731 antibody |
| Immunogen | Anti-Pdcd4 pS457 antibody was prepared from whole rabbit serum produced by repeated immunizations with a synthetic peptide corresponding to amino acids surrounding Ser457 in the human Pdcd4 protein.Immunogen Type: Peptide |
| Other Names | h731|MGC69337|PDCD4|D19Ucla1|Ma3|Tis|Dug|H731 |
| Gene, Accession # | Gene ID: 380222,27250,18569,64031 |
| Catalog # | ABIN1607873 |
| Price | |
| Order / More Info | Programmed Cell Death 4 (Neoplastic Transformation Inhibitor) (PDCD4) (Ser457), (phosphorylated) Antibody from ANTIBODIES-ONLINE GmbH |
| Product Specific References | n/a |
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