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RPGRIP1L
RPGRIP1 likeCORS3, FTM, JBTS7, KIAA1005, MKS5, NPHP8, PPP1R134
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). [provided by RefSeq, Jun 2016]
Top validated antibodies |
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| Proteintech Group |  55160-1-AP |
20 references | Polyclonal |
WB
EL
IP
IHC
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| Invitrogen Antibodies | 55160-1-AP |
Polyclonal |
WB
ICC
IP
IHC
OA
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| antibodies-online | ABIN2036007 |
Polyclonal |
WB
EL
IHC
FC
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| NovoPro Bioscience Inc. | 114805 |
Polyclonal |
WB
EL
IP
IHC
|
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| FineTest Biotech | FNab07404 |
Polyclonal |
WB
EL
IP
IHC
|
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