Protocadherin-15 (PCDH15) Peptide
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- Target See all PCDH15 products
- PCDH15 (Protocadherin-15 (PCDH15))
- Peptide Type
- Synthetic
- Origin
- Mammalian
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
- Sequence
- HSIVVQVQCI NKKVGTIIYH EVRIVVRDRN DNSPTFKHES YYATVNELTP
- Characteristics
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A synthetic peptide for use as a blocking control in assays to test for specificity of PCDH15 antibody,
Alternative Names: PCDH15 control peptide, PCDH15 antibody Blocking Peptide, Anti-PCDH15 Blocking Peptide, Protocadherin 15 Blocking Peptide, RP11-449J3.2 Blocking Peptide, DFNB23 Blocking Peptide, DKFZp667A1711 Blocking Peptide, USH1F Blocking Peptide, PCDH15, PCDH-15, PCDH 15, PCDH-15 Blocking Peptide, PCDH 15 Blocking Peptide - Purification
- Serum
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- Application Notes
- Optimal conditions should be determined by the investigator
- Restrictions
- For Research Use only
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- 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.
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- Target
- PCDH15 (Protocadherin-15 (PCDH15))
- Synonyms
- CDHR15 Peptide, DFNB23 Peptide, USH1F Peptide, BB078305 Peptide, ENSMUSG00000046980 Peptide, Gm9815 Peptide, Ush1f Peptide, av Peptide, nmf19 Peptide, protocadherin-15 Peptide, protocadherin related 15 Peptide, protocadherin-15 Peptide, protocadherin 15 Peptide, PCDH15 Peptide, CpipJ_CPIJ005081 Peptide, Pcdh15 Peptide
- Background
- PCDH15 is a member of the cadherin superfamily. Family members encode integral membrane proteins that mediate calcium-dependent cell-cell adhesion. PCDH15 consists of a signal peptide, 11 extracellular calcium-binding domains, a transmembrane domain and a unique cytoplasmic domain. It plays an essential role in maintenance of normal retinal and cochlear function. Mutations in this gene have been associated with hearing loss, which is consistent with its location at the Usher syndrome type 1F (USH1F) critical region on chromosome 10.
- Molecular Weight
- 80 kDa
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