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Invitrogen™ RPGRIP1L Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA5100049
Description
Antibody detects endogenous levels of total RPGRIP1L.
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 and Meckel syndrome type 5. Two transcript variants encoding different isoforms have been found for this gene.
Specifications
RPGRIP1L | |
Polyclonal | |
Unconjugated | |
RPGRIP1L | |
1700047E16Rik; 4931437C01; CORS3; DKFZp686C0668; fantom; fantom homolog; Ftm; JBTS7; KIAA1005; MKS5; Nephrocystin-8; NPHP8; PPP1R134; Protein fantom; protein phosphatase 1, regulatory subunit 134; RGD1311099; RPGR-interacting protein 1-like protein; RPGRIP1 like; RPGRIP1L; Rpgrip1-like; RPGRIP1-like protein | |
Rabbit | |
Affinity chromatography | |
RUO | |
23322, 244585, 307724 | |
-20°C | |
Liquid |
Immunohistochemistry (Paraffin), Western Blot, Immunocytochemistry | |
1 mg/mL | |
PBS with 50% glycerol and 0.02% sodium azide; pH 7.4 | |
Q68CZ1, Q8CG73 | |
RPGRIP1L | |
A synthesized peptide derived from human RPGRIP1L(Accession Q68CZ1), corresponding to amino acid residues E72-L122. | |
100 μL | |
Primary | |
Human, Mouse, Rat | |
Antibody | |
IgG |
Safety and Handling
WARNING: Cancer - www.P65Warnings.ca.gov
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