RPGRIP1L Antibody / Protein fantom
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).
Product Specifications
UniProt
Q68CZ1
Host
Rabbit
Immunogen
E. coli-derived recombinant human protein (amino acids E608-D1264) was used as the immunogen for the RPGRIP1L antibody.
Clonality
Polyclonal
Isotype
IgG
Applications
WB, FACS, Direct ELISA
Format
Antigen affinity purified
Buffer
0.5mg/ml if reconstituted with 0.2ml sterile DI water
Reconstitution
Limitations
This RPGRIP1L antibody is available for research use only.
Product Datasheet
https://cdn.gentaur.com/products/800/51409693/datasheet/rq7857.pdf
CAS Number
9007-83-4
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