
Phospho-SNAI1 (Ser246) Rabbit Polyclonal Antibody#abs130660
Please note that the price mentioned above is only for your reference. For detailed pricing information, kindly reach out to our sales representative, Vecent. We suggest contacting Vecent for an accurate quote. Data Examples Western blot analysis of SNAI1 phosphorylation expression in HT29 whole...
Description
Catalog-specification | Delivery time | USD price |
abs130660-50ug | 1-2 Weeks | 201 |
abs130660-100ug | 1-2 Weeks | 301 |
Please note that the price mentioned above is only for your reference. For detailed pricing information, kindly reach out to our sales representative, Vecent. We suggest contacting Vecent for an accurate quote.
Overview | |
Description | During postimplantation development, this protein plays multiple crucial roles. It not only participates in the formation and preservation of embryonic mesoderm but also potentially contributes to chondrogenesis and epithelial-mesenchymal inductive interactions. Its involvement spans various aspects of development and demonstrates its significance in these processes. |
Other names | The protein SNA is also known as Snail homolog 1 (SNAI1) or Snail 1 zinc finger protein. It is encoded by the SNAIL1 gene and is a transcriptional repressor that plays a crucial role in embryonic development, epithelial-mesenchymal transition, and tumor progression. SNA is homologous to the Snail protein found in Drosophila, hence the name Snail homolog 1 (Drosophila). Other names for SNA include SLUGH2, SNAI, snai1, SNAI1_HUMAN, Snail 1 homolog, and Zinc finger protein SNAI1. Its function is to regulate cell adhesion, migration, and differentiation by directly targeting E-cadherin, a cell-cell adhesion protein. SNA also interacts with other transcription factors, such as Twist and Slug, to regulate gene expression. Its overexpression has been implicated in multiple types of cancers, making it a potential target for cancer therapy. |
Source | Rabbit |
Specificity | The Phospho-SNAI1 (Ser246) Antibody specifically recognizes the phosphorylated Serine 246 residue on endogenous levels of SNAI1. It does not detect non-phosphorylated SNAI1. |
| Reactivity | Human;Mouse |
Predictive reaction species | Rabbit;Horse; |
| Antigen | SNAI1 |
Application | The recommended dilution for Western blot is 1:500-1:2000, for Immunofluorescence/Immunocytochemistry is 1:100-1:500, and for Enzyme-Linked Immunosorbent Assay using peptide is 1:20000-1:40000. You can obtain similar information by rearranging the text in different ways. |
| Immunogen | A synthesized peptide has been developed from the human SNAI1 protein, specifically targeting the phosphorylation site of Serine 246. The composition of the peptide closely resembles that of the original protein, ensuring its effectiveness in biological systems. This development marks an important step in understanding the function of the SNAI1 protein and its role in various pathological conditions. The use of synthetic peptides in research and clinical applications has proven to be a valuable tool for investigating the cell signaling pathways, protein-protein interactions and drug discovery. The synthesized peptide is expected to have potential applications in the development of novel therapies for various diseases. |
Properties | |
| MW | 29kDa |
| Concentration | 1mg/ml |
Purification | The purified rabbit serum was used to obtain the antibody through a process of sequential chromatography on affinity columns for phospho- and non-phospho-peptides. The resultant antibody is highly specific and of superior quality. |
Clonality | Polyclonal Antibody |
| Stability & Storage | To maintain the quality of the product, it is advised to store it at a temperature of -20 °C for a period of one year. It is important to avoid subjecting the product to multiple freeze/thaw cycles. |
Storage buffer | The storage condition for Rabbit IgG is as follows: it should be stored at a temperature of -20 °C in phosphate buffered saline with a pH of 7.4. Additionally, it should contain 150mM NaCl, 0.02% sodium azide, and 50% glycerol. It is important to note that this product remains stable for a period of 12 months starting from the date of receipt. |
Target | |
Background | The protein in question plays a pivotal role in many fundamental cellular processes such as embryonic mesoderm formation, induction of the epithelial to mesenchymal transition (EMT), cell migration, survival, and growth arrest. It binds to various gene promoters including the E-cadherin/CDH1 promoter, where it associates with histone demethylase, KDM1A, to initiate transcriptional repression and a decrease in dimethylated H3K4 levels. Additionally, it forms complexes with EGR1 and SP1 to up-regulate CDKN2B in response to tetradecanoyl phorbol acetate (TPA) exposure. It may also act as an individual activator of the CDKN2B promoter. In summary, the protein has a diverse array of functions in cellular processes such as gene transcription, cell migration, and growth control. |
Tissue specificity | Expressed in a variety of tissues with the highest expression in kidney. Expressed in mesenchymal and epithelial cell lines. |
| Posttranslational modification | Phosphorylated by GSK3B. Once phosphorylated, it becomes a target for BTRC ubiquitination. Phosphorylation by CSNK1E, probably at Ser-104, provides the priming site for the subsequent phosphorylation by GSK3B, probably at Ser-100 and Ser-96. Phosphorylation by PAK1 may modulate its transcriptional activity by promoting increased accumulation in the nucleus. Phosphorylation at Ser-11 and Ser-92 positively regulates its functions in induction of EMT and cell survival, respectively. Phosphorylation by LATS2, upon mitotic stress, oncogenic stress or Hippo pathway activation, occurs in the nucleus and promotes nuclear retention and stabilization of total cellular protein level.Ubiquitinated on Lys-98, Lys-137 and Lys-146 by FBXL14 and BTRC leading to degradation. BTRC-triggered ubiquitination requires previous GSK3B-mediated SNAI1 phosphorylation. Ubiquitination induced upon interaction with NOTCH1 or TP53/p53 is mediated by MDM2.O-GlcNAcylation at Ser-112 is enhanced in hyperglycaemic conditions, it opposes phosphorylation by GSK3B, and stabilizes the protein.ADP-ribosylation by PARP1 increases protein half-life and may be involved in TGFB-induced SNAI1 up-regulation. |
Celluar localization | Nucleus; |
| UniPort | O95863 |
Data Examples

Western blot analysis of SNAI1 phosphorylation expression in HT29 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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