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| Cat.No | ACP10668 | Target Name | TRIOBP |
|---|---|---|---|
| Target Synonyms | TRIOBP; KIAA1662; TARA; HRIHFB2122; TRIO and F-actin-binding protein; Protein Tara; Trio-associated repeat on actin | Form | Lyophilized powder |
| Expression System | Custom Production. Please inquire and provide the desire expression system. | Protein Length | Partial |
| Purity | >85% (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 | Q9H2D6 |
|---|
Uniprot Id
Q9H2D6
Target Species
Human
Target Name
TRIOBP
Target Full Name
TRIO and F-actin-binding protein
Target Function
May regulate actin cytoskeletal organization, cell spreading and cell contraction by directly binding and stabilizing filamentous F-actin. The localized formation of TARA and TRIO complexes coordinates the amount of F-actin present in stress fibers. May also serve as a linker protein to recruit proteins required for F-actin formation and turnover.
Target Involvement
Deafness, autosomal recessive, 28 (DFNB28)
Target Subcellular Location
Nucleus. Cytoplasm, cytoskeleton.; [Isoform 1]: Nucleus. Cytoplasm, cytoskeleton, microtubule organizing center, centrosome. Midbody.
Target Tissue Specificity
Widely expressed. Highly expressed in heart and placenta. Isoform 3 is expressed in fetal brain, retina and cochlea but is not detectable in the other tissues.
Target Synonyms
TRIOBP; KIAA1662; TARA; HRIHFB2122; TRIO and F-actin-binding protein; Protein Tara; Trio-associated repeat on actin
Target Background
This gene encodes a protein with an N-terminal pleckstrin homology domain and a C-terminal coiled-coil region. The protein interacts with trio, which is involved with neural tissue development and controlling actin cytoskeleton organization, cell motility and cell growth. The protein also associates with F-actin and stabilizes F-actin structures. Mutations in this gene have been associated with a form of autosomal recessive nonsyndromic deafness. Multiple alternatively spliced transcript variants that would encode different isoforms have been found for this gene, however some transcripts may be subject to nonsense-mediated decay (NMD).
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