![IHC-P analysis of human breast carcinoma tissue using GTX11901 AKT (phospho Ser473) antibody [104A282]. Dilution : 1:250 Antigen retrieval : Heat induced antigen retrieval (HIER) using 10mM sodium citrate buffer (pH 6.0) IHC-P analysis of human breast carcinoma tissue using GTX11901 AKT (phospho Ser473) antibody [104A282]. Dilution : 1:250 Antigen retrieval : Heat induced antigen retrieval (HIER) using 10mM sodium citrate buffer (pH 6.0)](https://www.genetex.com/upload/website/prouct_img/normal/GTX11901/GTX11901_377_IHC-P_w_23060519_696.webp)
IHC-P analysis of human breast carcinoma tissue using GTX11901 AKT (phospho Ser473) antibody [104A282]. Dilution : 1:250 Antigen retrieval : Heat induced antigen retrieval (HIER) using 10mM sodium citrate buffer (pH 6.0)
AKT (phospho Ser473) antibody [104A282]
GTX11901
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetAKT1
Overview
- SupplierGeneTex
- Product NameAKT (phospho Ser473) antibody [104A282] - Orthogonal Validated
- Delivery Days Customer9
- Application Supplier NoteIHC-P: 1:200 - 1:250. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
- ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
- CertificationResearch Use Only
- ClonalityMonoclonal
- Clone ID104A282
- Concentration1 mg/ml
- ConjugateUnconjugated
- Gene ID207
- Target nameAKT1
- Target descriptionAKT serine/threonine kinase 1
- Target synonymsAKT; AKT1m; PKB; PKB alpha; PKB-ALPHA; PRKBA; protein kinase B alpha; proto-oncogene c-Akt; RAC; rac protein kinase alpha; RAC-ALPHA; RAC-alpha serine/threonine-protein kinase; RAC-PK-alpha; serine-threonine protein kinase; v-akt murine thymoma viral oncogene homolog 1; v-akt murine thymoma viral oncogene-like protein 1
- HostMouse
- IsotypeIgG1
- Protein IDP31749
- Protein NameRAC-alpha serine/threonine-protein kinase
- Scientific DescriptionThe serine-threonine protein kinase encoded by the AKT1 gene is catalytically inactive in serum-starved primary and immortalized fibroblasts. AKT1 and the related AKT2 are activated by platelet-derived growth factor. The activation is rapid and specific, and it is abrogated by mutations in the pleckstrin homology domain of AKT1. It was shown that the activation occurs through phosphatidylinositol 3-kinase. In the developing nervous system AKT is a critical mediator of growth factor-induced neuronal survival. Survival factors can suppress apoptosis in a transcription-independent manner by activating the serine/threonine kinase AKT1, which then phosphorylates and inactivates components of the apoptotic machinery. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq]
- Storage Instruction-20°C or -80°C,2°C to 8°C
- UNSPSC12352203
References
- High Mobility Group A 1 Expression as a Poor Prognostic Marker Associated with Tumor Invasiveness in Gastric Cancer. Chang HP et al., 2022 May 9, Life (Basel)Read more
- The synthetic flavonoid WYC02-9 inhibits cervical cancer cell migration/invasion and angiogenesis via MAPK14 signaling. Chen YJ et al., 2013 Dec, Gynecol OncolRead more
- Antiparallel segregation of notch components in the immunological synapse directs reciprocal signaling in allogeneic Th:DC conjugates. Luty WH et al., 2007 Jul 15, J ImmunolRead more
- Silencing of caspase-8 and caspase-3 by RNA interference prevents vascular endothelial cell injury in mice with endotoxic shock. Matsuda N et al., 2007 Oct 1, Cardiovasc ResRead more
![IHC-P analysis of human breast carcinoma tissue using GTX11901 AKT (phospho Ser473) antibody [104A282]. Dilution : 1:250 Antigen retrieval : Heat induced antigen retrieval (HIER) using 10mM sodium citrate buffer (pH 6.0) IHC-P analysis of human breast carcinoma tissue using GTX11901 AKT (phospho Ser473) antibody [104A282]. Dilution : 1:250 Antigen retrieval : Heat induced antigen retrieval (HIER) using 10mM sodium citrate buffer (pH 6.0)](https://www.genetex.com/upload/website/prouct_img/normal/GTX11901/GTX11901_378_IHC-P_w_23060519_368.webp)
![WB analysis of 3T3 cells treated with and without PDGF (50 ng/ml) using GTX11901 AKT (phospho Ser473) antibody [104A282] and AKT1 antibody. Dilution : 2 microg/ml WB analysis of 3T3 cells treated with and without PDGF (50 ng/ml) using GTX11901 AKT (phospho Ser473) antibody [104A282] and AKT1 antibody. Dilution : 2 microg/ml](https://www.genetex.com/upload/website/prouct_img/normal/GTX11901/GTX11901_891_WB_w_23060519_790.webp)
![WB analysis of untreated (lane 1) and PDGF treated (lane 2) NIH-3T3 lysate using GTX11901 AKT (phospho Ser473) antibody [104A282]. Dilution : 2 microg/ml WB analysis of untreated (lane 1) and PDGF treated (lane 2) NIH-3T3 lysate using GTX11901 AKT (phospho Ser473) antibody [104A282]. Dilution : 2 microg/ml](https://www.genetex.com/upload/website/prouct_img/normal/GTX11901/GTX11901_892_WB_w_23060519_856.webp)
![WB analysis of NIH3T3 (1), HeLa (2),COS7 (3) and Jurkat (4) cell lysate using GTX82762 AKT1 antibody [3A3].](https://www.genetex.com/upload/website/prouct_img/normal/GTX82762/GTX82762_20170912_WB_w_23061322_461.webp)


![IP analysis of MCF-7 cells using GTX10438 AKT1 antibody [PKB-175]. Lane 1 : IP from MCF-7 cells using10 microL antibody Lane 2 : IP from MCF-7 cells using10 microL nonrelevant antibody Lane 3 : MCF-7 whole cell lysate](https://www.genetex.com/upload/website/prouct_img/normal/GTX10438/GTX10438_20170605_IP_w_23060120_654.webp)
