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| Cat.No | ACP00214 | Target Name | FBXO22 |
|---|---|---|---|
| Target Synonyms | F-box protein FBX22p44 | Form | Liquid or Lyophilized powder |
| Expression System | E.coli | Expression Range | 1-403aa |
| Mol Weight | 50.6 kDa | Protein Length | Full length |
| Purity | Greater than 85% as determined by SDS-PAGE. | Storage Buffer | 5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0. |
| Target Species | Human | Uniprot ID | Q8NEZ5 |
|---|
Uniprot Id
Q8NEZ5
Target Species
Human
Target Name
FBXO22
Target Full Name
F-box only protein 22
Target Function
Substrate-recognition component of the SCF (SKP1-CUL1-F-box protein)-type E3 ubiquitin ligase complex. Promotes the proteasome-dependent degradation of key sarcomeric proteins, such as alpha-actinin (ACTN2) and filamin-C (FLNC), essential for maintenance of normal contractile function.
Target Subcellular Location
Cytoplasm, myofibril, sarcomere, Z line.
Target Tissue Specificity
Predominantly expressed in liver, also enriched in cardiac muscle.
Target Research Area
Cell Biology
Target Synonyms
0610033L19Rik; 1600016C16Rik; F box only protein 22; F box protein 22; F box protein FBX22p44 ; F-box only protein 22; F-box protein FBX22p44; FBX22; FBX22_HUMAN; FBXO 22; FBXO22; FIST domain containing 1; FISTC1; FLJ13986; MGC124731; MGC31799
Target Background
This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class and, as a transcriptional target of the tumor protein p53, is thought to be involved in degradation of specific proteins in response to p53 induction. Alternative splicing results in multiple transcript variants.
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