Recombinant Human SIX1 protein (denatured) (His tag N-Terminus)
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Recombinant Human SIX1 protein (denatured) (His tag N-Terminus) is a Human Full Length protein, in the 1 to 284 aa range, expressed in Escherichia coli, with >85%, suitable for SDS-PAGE.
View Alternative Names
Homeobox protein SIX1, Sine oculis homeobox homolog 1, SIX1
- SDS-PAGE
Unknown
SDS-PAGE - Recombinant Human SIX1 protein (denatured) (His tag N-Terminus) (AB134521)
15% SDS-PAGE analysis of ab134521 (3ug)
Reactivity data
Sequence info
Properties and storage information
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
SIX1 influences cell proliferation survival and differentiation. As part of a transcriptional complex it interacts frequently with cofactors like EYA1 to execute its roles in developmental processes. These interactions allow SIX1 to impact gene targets that are important for tissue morphogenesis. The malfunctioning of these processes can lead to developmental disorders highlighting its role in the regulatory networks that govern organogenesis.
Pathways
Several essential biological processes involve SIX1 including the Wnt/β-catenin and TGF-β signaling pathways. In these pathways SIX1 sometimes regulates or interacts with proteins such as β-catenin enhancing transcriptional activation essential for cell fate determination. In the TGF-β pathway SIX1 influences epithelial-mesenchymal transition (EMT) an important event in embryogenesis and metastasis. These pathway involvements indicate its importance in maintaining cellular homeostasis and signaling balance.
Specifications
Form
Liquid
General info
Function
Transcription factor that is involved in the regulation of cell proliferation, apoptosis and embryonic development (By similarity). Plays an important role in the development of several organs, including kidney, muscle and inner ear (By similarity). Depending on context, functions as a transcriptional repressor or activator (By similarity). Lacks an activation domain, and requires interaction with EYA family members for transcription activation (PubMed : 15141091). Mediates nuclear translocation of EYA1 and EYA2 (PubMed : 19497856). Binds the 5'-TCA[AG][AG]TTNC-3' motif present in the MEF3 element in the MYOG promoter and CIDEA enhancer (PubMed : 15141091, PubMed : 19497856, PubMed : 23435380, PubMed : 27923061). Regulates the expression of numerous genes, including MYC, CCND1 and EZR (By similarity). Acts as an activator of the IGFBP5 promoter, probably coactivated by EYA2 (By similarity). Repression of precursor cell proliferation in myoblasts is switched to activation through recruitment of EYA3 to the SIX1-DACH1 complex (By similarity). During myogenesis, seems to act together with EYA2 and DACH2 (By similarity). Regulates the expression of CCNA1 (PubMed : 15123840). Promotes brown adipocyte differentiation (By similarity).
Sequence similarities
Belongs to the SIX/Sine oculis homeobox family.
Post-translational modifications
Phosphorylated during interphase; becomes hyperphosphorylated during mitosis. Hyperphosphorylation impairs binding to promoter elements.. Ubiquitinated by the anaphase promoting complex (APC), leading to its proteasomal degradation.
Subcellular localisation
Nucleus
Target data
Product promise
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