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ProteinTech/Phospho-AKT (Ser473) Monoclonal antibody/150ul/66444-1-Ig
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Tested ApplicationsPositive WB detected inCalyculin A treated HEK-293T cells, HEK-293 cells,Jurkat cells,Calyculin A treated PC-3 cells,TPA treated Jurkat cellsPositive IHC detected inhuman breast cancer tissueNote: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0Recommended dilutionApplicationDilutionWestern Blot (WB)WB : 1:2000-1:10000Immunohistochemistry (IHC)IHC : 1:100-1:400Sample-dependent, check data in validation data galleryPublished ApplicationsWBSee 200 publications belowIHCSee 22 publications belowIFSee 1 publications belowProduct Information66444-1-Ig targets Phospho-AKT (Ser473) inWB, IHC, IF, ELISA applications and shows reactivity with human,mouse samples.Tested Reactivityhuman,mouseCited Reactivity chicken, human, mouse, ratHost / IsotypeMouse / IgG1ClassMonoclonalTypeAntibodyImmunogenPeptideFull Namev-akt murine thymoma viral oncogene homolog 1Observed molecular weight 60-62 kDaGenBank accession numberNM_005163Gene symbolAKT1Gene ID (NCBI)207ConjugateUnconjugatedFormLiquidPurification MethodProtein A purificationStorage BufferPBS with 0.02% sodium azide and 50% glycerol pH 7.3.Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for-20oC storage.Background Information1) What is AKT?The serine/threonine kinase B AKT pathway (also known as the PI3K-Akt pathway) plays a vital role in the regulation of cellular processes, including cell proliferation, survival, and growth – processes that are essential for oncogenesis. Mutation of the regulator proteins PI3K and PTEN causes uncontrolled disruption within the PI3-kinase pathway, leading to the development of human cancers (1,2; see also AKT pathway poster for more details).2) phospho-AKT and FAQsA) What is the best way to normalize phosphorylated proteins analyzed by western blot?Normalize phospho-AKT and total AKT with your loading control (e.g. Actin, tubulin), then calculate the phospho/total ratio using these normalized values. Put more simply:1. Calculate the ratio of band intensities of a phospho-AKT band: the loading control.2. Calculate the ratio of band intensities of total AKT: loading control.3. Divide ratio obtained #1 by #2 to obtain a normalized value for comparison among different conditions. This procedure allows one to distinguish between a change in AKT expression and a change in the ratio of phospho-AKT.* If you are looking at the differences in a phospho-AKT expression resulting from an experimental condition (e.g., knockdown), you should also show the expression of total AKT to distinguish between a change in AKT expression (transcription/translation level) and a change in the AKT phosphorylation status.B) What is the observed molecular weight for AKT and phospho-AKT?Molecular Weight AKT – 56 kDaMolecular Weight phospho-AKT – 60 kDa (Figure 1)Figure 1. WB: HEK-293 cell lysate was subjected to SDS PAGE followed by western blot with 60203-2-Ig (AKT antibody) and 66444-1-Ig (AKT-phospho-S473 antibody) at a dilution of 1:4000 incubated at room temperature for 1.5 hours.C) Are there any special WB conditions to optimize staining of a phospho-AKT?Since this is a phosphorylated protein, 5% BSA is recommended over non-fat milk as a blocking agent.D) What are good positive and negative controls for a phospho-AKT?- Positive Control: HEK293 cells- Negative Control: Treatment with PI3K inhibitors (e.g. wortmannin)E) What species does this antibody react with?Our internal testing has confirmed that it reacts with the human and mouse forms of phospho-AKT.Reactivity with the human form is also supported by the literature’s citations of this antibody.References:1. Perturbations of the AKT signaling pathway in human cancer.2. Targeting the PI3K-Akt pathway in human cancer: rationale and promise.ProtocolsProduct Specific ProtocolsWB protocol for Phospho-AKT (Ser473) antibody 66444-1-IgDownload protocolIHC protocol for Phospho-AKT (Ser473) antibody 66444-1-IgDownload protocolStandard ProtocolsClick here to view our Standard Protocols
Proteintech Group 由一群当时积极从事 NIH 资助研究的科学家于 2001 年创立。最初的创始人之一和现任首席执行官 Jason Li 博士在公司成立期间是伊利诺伊大学芝加哥分校的免疫学副教授。他谈到 Proteintech 成立背后的原因:
“我们抱负的核心是一家由科学家组成的公司;一家为研究人员提供优势的抗体供应商,而不是投资者。”
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