SLC26A5 Antibody (PACO20496)
- SKU:
- PACO20496
- Product Type:
- Antibody
- Reactivity:
- Human
- Mouse
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Applications:
- ELISA
- WB
- Antibody Type:
- Polyclonal Antibody
- Conjugation:
- Unconjugated
Frequently bought together:
Description
SLC26A5 Antibody (PACO20496)
The SLC26A5 Polyclonal Antibody (PACO20496) is a valuable tool for researchers studying SLC26A5, a protein involved in ion transport in the inner ear. This antibody, produced in rabbits, exhibits high reactivity with human samples and has been validated for use in Western blot applications. By binding specifically to the SLC26A5 protein, this antibody enables precise detection and analysis in various cell types, making it an essential component for investigations in auditory physiology and related fields.
SLC26A5, also known as prestin, is crucial for the function of outer hair cells in the cochlea, where it is responsible for electromotility and the amplification of sound signals. Understanding the role of SLC26A5 is key to unraveling the mechanisms of hearing and developing treatments for hearing disorders. Research targeting SLC26A5 has the potential to advance our knowledge of auditory function and contribute to the development of innovative therapies for hearing loss and other related conditions.
| Antibody Name: | SLC26A5 Antibody (PACO20496) |
| Antibody SKU: | PACO20496 |
| Size: | 50ul |
| Host Species: | Rabbit |
| Tested Applications: | ELISA, WB |
| Recommended Dilutions: | ELISA:1:1000-1:2000, WB:1:200-1:1000 |
| Species Reactivity: | Human, Mouse, Rat |
| Immunogen: | Synthetic peptide of human SLC26A5 |
| Form: | Liquid |
| Storage Buffer: | -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol |
| Purification Method: | Antigen affinity purification |
| Clonality: | Polyclonal |
| Isotype: | IgG |
| Conjugate: | Non-conjugated |
 | Gel: 6%SDS-PAGE,Lysate: 40 μgPrimary antibody: PACO20496(SLC26A5 Antibody) at dilution 1/200 dilution,Secondary antibody: Goat anti rabbit IgG at 1/8000 dilution,Exposure time: 3 minutes. |
| Background: | This gene encodes a member of the SLC26A/SulP transporter family. The protein functions as a molecular motor in motile outer hair cells (OHCs) of the cochlea, inducing changes in cell length that act to amplify sound levels. The transmembrane protein is an incomplete anion transporter, and does not allow anions to cross the cell membrane but instead undergoes a conformational change in response to changes in intracellular Cl- levels that results in a change in cell length. |
| Synonyms: | solute carrier family 26 (anion exchanger), member 5 |
| UniProt Protein Function: | 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, it can operate at microsecond rates. It uses cytoplasmic anions as extrinsic voltage sensors, probably chloride and bicarbonate. After binding to a site with millimolar affinity, these anions are translocated across the membrane in response to changes in the transmembrane voltage. They move towards the extracellular surface following hyperpolarization, and towards the cytoplasmic side in response to depolarization. As a consequence, this translocation triggers conformational changes in the protein that ultimately alter its surface area in the plane of the plasma membrane. The area decreases when the anion is near the cytoplasmic face of the membrane (short state), and increases when the ion has crossed the membrane to the outer surface (long state). So, it 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. Salicylate, an inhibitor of outer hair cell motility, acts as competitive antagonist at the prestin anion-binding site (). |
| UniProt Protein Details: | |
| NCBI Summary: | This gene encodes a member of the SLC26A/SulP transporter family. The protein functions as a molecular motor in motile outer hair cells (OHCs) of the cochlea, inducing changes in cell length that act to amplify sound levels. The transmembrane protein is an incomplete anion transporter, and does not allow anions to cross the cell membrane but instead undergoes a conformational change in response to changes in intracellular Cl- levels that results in a change in cell length. The protein functions at microsecond rates, which is several orders of magnitude faster than conventional molecular motor proteins. Mutations in this gene are potential candidates for causing neurosensory deafness. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Nov 2009] |
| UniProt Code: | P58743 |
| NCBI GenInfo Identifier: | 269784651 |
| NCBI Gene ID: | 375611 |
| NCBI Accession: | NP_001161434.1 |
| UniProt Secondary Accession: | P58743,Q496J2, Q7Z7F3, Q86UF8, Q86UF9, Q86UG0 |
| UniProt Related Accession: | P58743 |
| Molecular Weight: | 81 kDa |
| NCBI Full Name: | prestin isoform e |
| NCBI Synonym Full Names: | solute carrier family 26 member 5 |
| NCBI Official Symbol: | SLC26A5Â Â |
| NCBI Official Synonym Symbols: | PRES; DFNB61Â Â |
| NCBI Protein Information: | prestin |
| UniProt Protein Name: | Prestin |
| UniProt Synonym Protein Names: | Solute carrier family 26 member 5 |
| Protein Family: | Prestin |
| UniProt Gene Name: | SLC26A5Â Â |
| UniProt Entry Name: |
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