Solute Carrier Family 26, Member 5 (Prestin) (SLC26A5) Peptide
-
- Target See all SLC26A5 products
- SLC26A5 (Solute Carrier Family 26, Member 5 (Prestin) (SLC26A5))
- Peptide Type
- Synthetic
- Origin
- Mammalian
-
Source
- Synthetic
- Application
- Blocking Peptide (BP), Immunohistochemistry (IHC), Western Blotting (WB)
- Sequence
- FSVTISMAKT LANKHGYQVD GNQELIALGL CNSIGSLFQT FSISCSLSRS
- Characteristics
-
A synthetic peptide for use as a blocking control in assays to test for specificity of SLC26 A5 antibody,
Alternative Names: SLC26A5 control peptide, SLC26A5 antibody Blocking Peptide, Anti-SLC26A5 Blocking Peptide, Solute Carrier Family 26 Member 5 Blocking Peptide, Prestin Blocking Peptide, DFNB61 Blocking Peptide, MGC118886 Blocking Peptide, MGC118887 Blocking Peptide, MGC118888 Blocking Peptide, MGC118889 Blocking Peptide, PRES Blocking Peptide, SLC26A5, SLCA5-26, SLCA5 26, SLCA5-26 Blocking Peptide, SLCA5 26 Blocking Peptide
-
-
- Application Notes
- Optimal conditions should be determined by the investigator
- Restrictions
- For Research Use only
-
- Format
- Lyophilized
- Reconstitution
- Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
- Buffer
- PBS
- Handling Advice
- Avoid repeated freeze/thaw cycles.
- Storage
- -20 °C
- Storage Comment
- Store at -20 °C long term.
-
- Target
- SLC26A5 (Solute Carrier Family 26, Member 5 (Prestin) (SLC26A5))
- Synonyms
- 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
- Background
- 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.
- Molecular Weight
- 81 kDa
-