PLS1
Plastins are a family of actin-binding proteins that are conserved throughout eukaryote evolution and expressed in most tissues of higher eukaryotes. In humans, two ubiquitous plastin isoforms (L and T) have been identified. The protein encoded by this gene is a third distinct plastin isoform, which is specifically expressed at high levels in the small intestine. Alternatively spliced transcript variants varying in the 5' UTR, but encoding the same protein, have been found for this gene. [provided by RefSeq]
Full Name
plastin 1 (I isoform)
Function
Actin-bundling protein. In the inner ear, it is required for stereocilia formation. Mediates liquid packing of actin filaments that is necessary for stereocilia to grow to their proper dimensions.
Biological Process
Actin filament bundle assemblyManual Assertion Based On ExperimentIBA:GO_Central
Actin filament network formationManual Assertion Based On ExperimentIBA:GO_Central
Auditory receptor cell stereocilium organizationISS:UniProtKB
Intestinal D-glucose absorptionIEA:Ensembl
Positive regulation of multicellular organism growthIEA:Ensembl
Positive regulation of protein localization to plasma membraneISS:UniProtKB
Regulation of microvillus lengthIEA:Ensembl
Terminal web assemblyIEA:Ensembl
Vestibular receptor cell stereocilium organizationISS:UniProtKB
Actin filament network formationManual Assertion Based On ExperimentIBA:GO_Central
Auditory receptor cell stereocilium organizationISS:UniProtKB
Intestinal D-glucose absorptionIEA:Ensembl
Positive regulation of multicellular organism growthIEA:Ensembl
Positive regulation of protein localization to plasma membraneISS:UniProtKB
Regulation of microvillus lengthIEA:Ensembl
Terminal web assemblyIEA:Ensembl
Vestibular receptor cell stereocilium organizationISS:UniProtKB
Cellular Location
Cytoplasm
Cell projection, stereocilium
Cell projection, stereocilium
Involvement in disease
Deafness, autosomal dominant, 76 (DFNA76):
A form of non-syndromic deafness characterized by mild to profound sensorineural hearing loss and variable age at onset. Sensorineural hearing loss results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information.
A form of non-syndromic deafness characterized by mild to profound sensorineural hearing loss and variable age at onset. Sensorineural hearing loss results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information.
PTM
Phosphorylated.
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Anti-PLS1 antibodies
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Target: PLS1
Host: Mouse
Antibody Isotype: IgG2b, κ
Specificity: Human
Clone: 3G10
Application*: WB
More Infomation
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For Research Use Only. Not For Clinical Use.
(P): Predicted
* Abbreviations
- AActivation
- AGAgonist
- APApoptosis
- BBlocking
- BABioassay
- BIBioimaging
- CImmunohistochemistry-Frozen Sections
- CIChromatin Immunoprecipitation
- CTCytotoxicity
- CSCostimulation
- DDepletion
- DBDot Blot
- EELISA
- ECELISA(Cap)
- EDELISA(Det)
- ESELISpot
- EMElectron Microscopy
- FFlow Cytometry
- FNFunction Assay
- GSGel Supershift
- IInhibition
- IAEnzyme Immunoassay
- ICImmunocytochemistry
- IDImmunodiffusion
- IEImmunoelectrophoresis
- IFImmunofluorescence
- IGImmunochromatography
- IHImmunohistochemistry
- IMImmunomicroscopy
- IOImmunoassay
- IPImmunoprecipitation
- ISIntracellular Staining for Flow Cytometry
- LALuminex Assay
- LFLateral Flow Immunoassay
- MMicroarray
- MCMass Cytometry/CyTOF
- MDMeDIP
- MSElectrophoretic Mobility Shift Assay
- NNeutralization
- PImmunohistologyp-Paraffin Sections
- PAPeptide Array
- PEPeptide ELISA
- PLProximity Ligation Assay
- RRadioimmunoassay
- SStimulation
- SESandwich ELISA
- SHIn situ hybridization
- TCTissue Culture
- WBWestern Blot
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