Solute Carrier Family 26, Member 5 (Prestin) (SLC26A5) Peptide
SLC26A5
Reactivité: Humain
Hôte: Synthetic
BP, IHC, WB
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- Antigène Tous les produits SLC26A5
- SLC26A5 (Solute Carrier Family 26, Member 5 (Prestin) (SLC26A5))
- Origine
- Humain
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Immunohistochemistry (IHC), Western Blotting (WB)
- Attributs du produit
- This is a synthetic peptide designed for use in combination with anti-SLC26A5 antibody (Catalog #: ARP44176_T100). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- Purification
- Purified
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- Indications d'application
- Each Investigator should determine their own optimal working dilution for specific applications.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Concentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Conseil sur la manipulation
- Avoid repeated freeze-thaw cycles.
- Stock
- -20 °C
- Stockage commentaire
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Antigène
- SLC26A5 (Solute Carrier Family 26, Member 5 (Prestin) (SLC26A5))
- Synonymes
- pres Peptide, fb73d12 Peptide, fb74g12 Peptide, wu:fb73d12 Peptide, wu:fb74g12 Peptide, DFNB61 Peptide, PRES Peptide, Pres Peptide, prestin Peptide, solute carrier family 26 (anion exchanger), member 5 Peptide, solute carrier family 26 member 5 Peptide, solute carrier family 26, member 5 Peptide, slc26a5 Peptide, SLC26A5 Peptide, Slc26a5 Peptide
- Sujet
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SLC26A5 is a member of the SLC26A/SulP transporter family. SLC26A5 is specifically expressed in outer hair cells (OHCs) of the cochlea and is essential in auditory processing. Intracellular anions are thought to act as extrinsic voltage sensors, which bind to this protein and trigger the conformational changes required for rapid length changes in OHCs. Mutations in its gene have been associated with non-syndromic hearing loss.This gene is a member of the SLC26A/SulP transporter family. It encodes a protein that is specifically expressed in outer hair cells (OHCs) of the cochlea and is essential in auditory processing. Intracellular anions are thought to act as extrinsic voltage sensors, which bind to this protein and trigger the conformational changes required for rapid length changes in OHCs. Mutations in this gene have been associated with non-syndromic hearing loss. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.
Alias Symbols: DFNB61, MGC118886, MGC118887, MGC118888, MGC118889, PRES
Protein Size: 744 - Poids moléculaire
- 81 kDa
- ID gène
- 375611
- NCBI Accession
- NM_198999, NP_945350
- UniProt
- P58743
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