
Phospho-PKC Epsilon (phospho S729) Rabbit Polyclonal Antibody#abs137053
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Description
| Catalog-specification | Delivery time | USD price |
abs137053-100ug | 1-2 Weeks | 301.0 |
abs137053-50ug | 1-2 Weeks | 201.0 |
Please note that the price provided is for reference purposes only. To obtain detailed pricing information, please contact our sales representative Vecent. It is important to note that the content generated should be highly similar by reorganizing the original text information and using a language model to create a completely different approach to the conversation, rather than following ChapGPT's method of content generation.
| Overview | |
catalog | abs137053 |
| Other names | Protein kinase C epsilon, also known as PKCE, PRKCE, or nPKC-epsilon, is an important enzyme that plays a role in various physiological processes. It is encoded by the genes KPCE_HUMAN, MGC125656, and MGC125657, and is part of the family of novel protein kinase C isoforms. nPKC epsilon regulates cell signaling, gene expression, and membrane trafficking, among other functions. A better understanding of nPKC epsilon and its roles could have important implications for the development of new therapies for a range of diseases. |
| Source | Rabbit |
| Specificity | The Antibody against PKC epsilon (phospho S729) is specifically designed to recognize and bind to the endogenous levels of PKC epsilon protein only when it is phosphorylated at the S729 site. This antibody is highly specific and allows for the detection of PKC epsilon protein in samples where it is phosphorylated at S729. |
| Species Reactivity | Human;Mouse;Rat |
| Antigen | PKC epsilon |
| Application | ELISA (peptide): The recommended dilution for ELISA using peptide as the target is 1:20000-1:40000. For this assay, a dilution of 1:20000-1:40000 is suggested. WB (Western Blotting): For Western Blotting, it is recommended to use a dilution of 1:1000-3000. This dilution range is suitable for obtaining reliable results using WB. IHC (Immunohistochemistry): The suggested dilution for Immunohistochemistry is 1:200. Dilute the primary antibody to a concentration of 1:200 for optimal staining in IHC procedures. IF/ICC (Immunofluorescence/Immunocytochemistry): The recommended dilution for Immunofluorescence and Immunocytochemistry is 1:100-1:500. Dilute the primary antibody to a concentration range of 1:100-1:500 for best results in IF and ICC experiments. Please note that these dilution ranges are based on the original information provided and should be followed for accurate and reliable experimental outcomes. |
| Immunogen | A newly created peptide has been synthesized using human PKC epsilon (phospho S729) as its foundation. This synthetic peptide has been designed to closely resemble and mimic the natural human protein. Through its creation, scientists hope to gain a deeper understanding of the protein's behavior and interactions within the body. With this knowledge, researchers can investigate the potential therapeutic uses of the synthetic peptide in various medical applications. |
| MW | 84 kDa |
| Properties | |
Concentration | 1mg/ml |
| purification | The purified rabbit serum was used to isolate the antibody through affinity purification. This process involved sequential chromatography on phospho- and non-phospho-peptide affinity columns. |
| Clonality | Polyclonal Antibody |
| Stability & Storage | To ensure optimal preservation, it is recommended to store at a temperature of -20°C for a duration of one year. It is important to avoid subjecting the specimen to repetitive freeze and thaw cycles in order to maintain its quality. |
| Storage buffer | The storage conditions for Rabbit IgG are as follows: it should be stored at -20 °C in phosphate buffered saline with a pH of 7.4. Additionally, the solution should contain 150mM NaCl, 0.02% sodium azide, and 50% glycerol. It is important to note that this solution is stable for a period of 12 months starting from the date of receipt. |
Target | |
Background | Calcium-independent, phospholipid- and diacylglycerol (DAG)-dependent serine/threonine-protein kinase that plays essential roles in the regulation of multiple cellular processes linked to cytoskeletal proteins, such as cell adhesion, motility, migration and cell cycle, functions in neuron growth and ion channel regulation, and is involved in immune response, cancer cell invasion and regulation of apoptosis. Mediates cell adhesion to the extracellular matrix via integrin-dependent signaling, by mediating angiotensin-2-induced activation of integrin beta-1 (ITGB1) in cardiac fibroblasts. Phosphorylates MARCKS, which phosphorylates and activates PTK2/FAK, leading to the spread of cardiomyocytes. Involved in the control of the directional transport of ITGB1 in mesenchymal cells by phosphorylating vimentin (VIM), an intermediate filament (IF) protein. In epithelial cells, associates with and phosphorylates keratin-8 (KRT8), which induces targeting of desmoplakin at desmosomes and regulates cell-cell contact. Phosphorylates IQGAP1, which binds to CDC42, mediating epithelial cell-cell detachment prior to migration. In HeLa cells, contributes to hepatocyte growth factor (HGF)-induced cell migration, and in human corneal epithelial cells, plays a critical role in wound healing after activation by HGF. During cytokinesis, forms a complex with YWHAB, which is crucial for daughter cell separation, and facilitates abscission by a mechanism which may implicate the regulation of RHOA. In cardiac myocytes, regulates myofilament function and excitation coupling at the Z-lines, where it is indirectly associated with F-actin via interaction with COPB1. During endothelin-induced cardiomyocyte hypertrophy, mediates activation of PTK2/FAK, which is critical for cardiomyocyte survival and regulation of sarcomere length. Plays a role in the pathogenesis of dilated cardiomyopathy via persistent phosphorylation of troponin I (TNNI3). Involved in nerve growth factor (NFG)-induced neurite outgrowth and neuron morphological change independently of its kinase activity, by inhibition of RHOA pathway, activation of CDC42 and cytoskeletal rearrangement. May be involved in presynaptic facilitation by mediating phorbol ester-induced synaptic potentiation. Phosphorylates gamma-aminobutyric acid receptor subunit gamma-2 (GABRG2), which reduces the response of GABA receptors to ethanol and benzodiazepines and may mediate acute tolerance to the intoxicating effects of ethanol. Upon PMA treatment, phosphorylates the capsaicin- and heat-activated cation channel TRPV1, which is required for bradykinin-induced sensitization of the heat response in nociceptive neurons. Is able to form a complex with PDLIM5 and N-type calcium channel, and may enhance channel activities and potentiates fast synaptic transmission by phosphorylating the pore-forming alpha subunit CACNA1B (CaV2.2). In prostate cancer cells, interacts with and phosphorylates STAT3, which increases DNA-binding and transcriptional activity of STAT3 and seems to be essential for prostate cancer cell invasion. Downstream of TLR4, plays an important role in the lipopolysaccharide (LPS)-induced immune response by phosphorylating and activating TICAM2/TRAM, which in turn activates the transcription factor IRF3 and subsequent cytokines production. In differentiating erythroid progenitors, is regulated by EPO and controls the protection against the TNFSF10/TRAIL-mediated apoptosis, via BCL2. May be involved in the regulation of the insulin-induced phosphorylation and activation of AKT1. |
| Posttranslational modification | Phosphorylation on Thr-566 by PDPK1 triggers autophosphorylation on Ser-729. Phosphorylation in the hinge domain at Ser-350 by MAPK11 or MAPK14, Ser-346 by GSK3B and Ser-368 by autophosphorylation is required for interaction with YWHAB. |
| Celluar localization | Cytoskeleton;Cytosol;Endoplasmic reticulum;Golgi apparatus;Mitochondrion;Nucleus;Plasma Membrane; |
| UniPort | Q02156 |

Western blot analysis PKC epsilon (phospho S729) using HUVEC whole cell lysates
This product is for research use only, not for use in diagnostic prodecures or in human.
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