RPGRIP1-Like (RPGRIP1L) (Middle Region) Peptid
RPGRIP1L
Reaktivität: Human
Wirt: Synthetic
BP, WB
Produktnummer ABIN5672173
Kurzübersicht für RPGRIP1-Like (RPGRIP1L) (Middle Region) Peptid (ABIN5672173)
Target
RPGRIP1L
(RPGRIP1-Like (RPGRIP1L))
Spezies
Human
Quelle
Synthetic
Applikation
Blocking Peptide (BP), Western Blotting (WB)
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Protein Region
- Middle Region
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Sequenz
- VLAPRPKPRQ RLTPVDKKVS FVDIMPHQSD ETSPPPEDRK EISPEVEHIP
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Produktmerkmale
- 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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RPGRIP1-Like (RPGRIP1L) peptide
RPGRIP1L Reaktivität: Human, Hund Wirt: Synthetic BP, Imm
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Applikationshinweise
- Optimal working dilution should be determined by the investigator.
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Lyophilized
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Rekonstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
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Lagerung
- -20 °C
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Informationen zur Lagerung
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- RPGRIP1L (RPGRIP1-Like (RPGRIP1L))
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Hintergrund
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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 -
Gen-ID
- 23322
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NCBI Accession
- NM_001127897, NP_001121369
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UniProt
- Q68CZ1
Target
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