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MilliporeSigma™ Mouse anti-Prestin, Clone: 3A2.2,

Catalog No. MABN746MI Shop All MilliporeSigma Products
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Mouse Monoclonal Antibody

Specifically detects Prestin clone: 3A2.2 in Mouse samples, and it is validated for Western Blotting

Prestin is a motor protein that converts auditory stimuli to length changes in outer hair cells and mediates sound amplification in the mammalian hearing organ. Prestin is a bidirectional voltage-to-force converter that can operate at microsecond rates. It uses cytoplasmic anions as extrinsic voltage sensors, probably chloride and bicarbonate to translocate anions toward or away from the extracellular plasma membrane surface. As a consequence, this translocation triggers conformational changes in Prestin that ultimately alter its surface area in the plane of the plasma membrane. Prestin acts as an incomplete transporter. It swings anions across the membrane, but does not allow these anions to dissociate and escape to the extracellular space and in that process it helps to modulate the electro-physical signals necessary for hearing. Prestin is expressed in outer hair cells and localized to the cell membrane. Mutations in Prestin can lead to deafness.
TRUSTED_SUSTAINABILITY

Specifications

Antigen Prestin
Applications Western Blot
Classification Monoclonal
Clone 3A2.2
Formulation Purified mouse monoclonal IgMκ in buffer containing PBS with 0.05% sodium azide.
Gene Accession No. P58743
Gene Symbols SLC26A5; PRES
Host Species Mouse
Immunogen Linear peptide corresponding to human Prestin.
Purification Method Purified by Ion-Exchange Chromatography
Quantity 100 μg
Regulatory Status RUO
Research Discipline Neuroscience
Primary or Secondary Primary
Gene ID (Entrez) NP_001161434
Target Species Mouse
Content And Storage Stable for one year at 2°C to 8°C from date of receipt.
Form Purified
Isotype IgM κ
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