
Phospho-C/EBP- Alpha (Ser21) Rabbit Polyclonal Antibody#abs130958
Please note that the price mentioned above is only for your reference. For detailed pricing information, we recommend that you contact our seller, Vecent. Thank you. Data Examples Western blot analysis of C/EBP- alpha phosphorylation expression in EGF treated HepG2 whole cell lysates,The lane on...
Description
Catalog-specification | Delivery time | USD price |
abs130958-50ug | 1-2 Weeks | 201 |
abs130958-100ug | 1-2 Weeks | 301 |
Please note that the price mentioned above is only for your reference. For detailed pricing information, we recommend that you contact our seller, Vecent. Thank you.
Overview | |
Description | This intronless gene encodes a bZIP transcription factor, which plays a vital role in gene regulation. It exhibits the ability to bind to specific promoters and enhancers either as a homodimer or by forming heterodimers with CEBP-beta and CEBP-gamma, proteins that are closely related. Research has demonstrated that this encoded protein can interact with the promoter region and effectively control the expression of the leptin gene. Leptin is a crucial protein involved in maintaining body weight homeostasis. By modulating its expression, the encoded protein contributes to the regulation of body weight. |
Other names | Here are some variations of the text: |
Source | Rabbit |
Specificity | The antibody Phospho-C/EBP-alpha (Ser21) is capable of detecting levels of endogenous C/EBP-alpha specifically when it is phosphorylated at Serine 21. To emphasize, the generated content should not follow the format and structure of the original text, rather, it should provide a completely different perspective using a language model. |
| Reactivity | Human;Mouse;Rat |
Predictive reaction species | Pig;Bovine; |
| Antigen | C/EBP-α |
Application | The recommended dilution ranges for WB are 1:500-1:2000, for IHC are 1:50-1:200, for IF/ICC are 1:100-1:500, and for ELISA(peptide) are 1:20000-1:40000. These dilution ranges ensure optimal results and reliable data for each respective assay. It is important to follow these recommendations to achieve accurate and reproducible results in your experiments. Diluting the samples within these ranges will allow for the detection and quantification of your target of interest while minimizing background signal. |
| Immunogen | A peptide that has been synthesized from human C/EBP-alpha, specifically around the phosphorylation site of Serine 21, has been developed. The content generated from this information must be highly similar but with rearranged wording. |
Properties | |
| MW | 45kDa |
| Concentration | 1mg/ml |
Purification | ,。,,。 |
Clonality | Polyclonal Antibody |
| Stability & Storage | One year storage is recommended at -20 °C. It is important to prevent repeated freezing and thawing cycles. Please ensure that the content generated is not in the format of a conversation but rather a completely different way of speaking using the language model. |
Storage buffer | :IgG-20°C,,pH7.4,150mM,0.02%50%。12。 |
Target | |
Background | Transcription factor that coordinates proliferation arrest and the differentiation of myeloid progenitors, adipocytes, hepatocytes, and cells of the lung and the placenta. Binds directly to the consensus DNA sequence 5'-T[TG]NNGNAA[TG]-3' acting as an activator on distinct target genes (PubMed:11242107). During early embryogenesis, plays essential and redundant functions with CEBPB. Essential for the transition from common myeloid progenitors (CMP) to granulocyte/monocyte progenitors (GMP). Critical for the proper development of the liver and the lung (By similarity). Necessary for terminal adipocyte differentiation, is required for postnatal maintenance of systemic energy homeostasis and lipid storage (By similarity). To regulate these different processes at the proper moment and tissue, interplays with other transcription factors and modulators. Downregulates the expression of genes that maintain cells in an undifferentiated and proliferative state through E2F1 repression, which is critical for its ability to induce adipocyte and granulocyte terminal differentiation. Reciprocally E2F1 blocks adipocyte differentiation by binding to specific promoters and repressing CEBPA binding to its target gene promoters. Proliferation arrest also depends on a functional binding to SWI/SNF complex (PubMed:14660596). In liver, regulates gluconeogenesis and lipogenesis through different mechanisms. To regulate gluconeogenesis, functionally cooperates with FOXO1 binding to IRE-controlled promoters and regulating the expression of target genes such as PCK1 or G6PC. To modulate lipogenesis, interacts and transcriptionally synergizes with SREBF1 in promoter activation of specific lipogenic target genes such as ACAS2. In adipose tissue, seems to act as FOXO1 coactivator accessing to ADIPOQ promoter through FOXO1 binding sites (By similarity). |
| Posttranslational modification | Phosphorylation at Ser-190 is required for interaction with CDK2, CDK4 and SWI/SNF complex leading to cell cycle inhibiton. Dephosphorylated at Ser-190 by protein phosphatase 2A (PP2A) through PI3K/AKT signaling pathway regulation (PubMed:15107404). Phosphorylation at Thr-226 and Thr-230 by GSK3 is constitutive in adipose tissue and lung. In liver, both Thr-226 and Thr-230 are phosphorylated only during feeding but not during fasting. Phosphorylation of the GSK3 consensus sites selectively decreases transactivation activity on IRE-controlled promoters.Sumoylated, sumoylation blocks the inhibitory effect on cell proliferation by disrupting the interaction with SMARCA2.Ubiquitinated by RFWD2/COP1 upon interaction with TRIB1. |
Celluar localization | Nucleus; |
| UniPort | P49715 |
Data Examples

Western blot analysis of C/EBP- alpha phosphorylation expression in EGF treated HepG2 whole cell lysates,The lane on the left is treated with the antigen-specific peptide.
This product is for research use only, not for use in diagnostic prodecures or in human.
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