RPGRIP1-Like (RPGRIP1L) (Middle Region) Peptide
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- Target See all RPGRIP1L products
- RPGRIP1L (RPGRIP1-Like (RPGRIP1L))
- Protein Region
- Middle Region
- Origin
- Human
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Sequence
- VLAPRPKPRQ RLTPVDKKVS FVDIMPHQSD ETSPPPEDRK EISPEVEHIP
- Characteristics
- This is a synthetic peptide designed for use in combination with anti- RPGRIP1L Antibody. 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.
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- Application Notes
- Optimal working dilution should be determined by the investigator.
- 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.
- Storage
- -20 °C
- Storage Comment
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- RPGRIP1L (RPGRIP1-Like (RPGRIP1L))
- Synonyms
- si:ch1073-301i20.1 Peptide, mks5 Peptide, cors3 Peptide, jbts7 Peptide, nphp8 Peptide, CORS3 Peptide, FTM Peptide, JBTS7 Peptide, MKS5 Peptide, NPHP8 Peptide, 1700047E16Rik Peptide, 4931437C01 Peptide, Ftm Peptide, Nphp8 Peptide, RGD1311099 Peptide, RPGRIP1 like Peptide, RPGRIP1-like Peptide, Protein fantom Peptide, Rpgrip1-like Peptide, RPGRIP1L Peptide, rpgrip1l Peptide, mks-5 Peptide, Rpgrip1l Peptide
- Background
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The protein encoded by this gene can localize to the basal body-centrosome complex or to primary cilia and centrosomes in ciliated cells. The encoded protein has been found to interact with nephrocystin-4. Defects in this gene are a cause of Joubert syndrome type 7 (JBTS7) and Meckel syndrome type 5 (MKS5). Two transcript variants encoding different isoforms have been found for this gene.
Alias Symbols: FTM, MKS5, CORS3, JBTS7, NPHP8, PPP1R134
Protein Size: 1315 - Gene ID
- 23322
- NCBI Accession
- NM_001127897, NP_001121369
- UniProt
- Q68CZ1
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