RPGRIP1L 产品
(RPGRIP1-Like (RPGRIP1L))
Categories
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. [provided by RefSeq, Jul 2008].
antibodies-online.com stands for high-quality research products. Search, find and order tools with extensive validation data, images, references. Our scientific customer service is always at your disposal if you have any questions about the selection or application of our products.
Featured RPGRIP1L Categories
RPGRIP1L 抗体
High quality antibodies with extensive validation data.
Recommended RPGRIP1L 抗体
Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human, Mouse, Rat
Application
WB, IHC, ICC, IF
Validations
- (3)
Cat. No.
ABIN6264825
Quantity
100 μL
Datasheet
Datasheet
Reactivity
Human
Application
WB, ELISA
Validations
- (1)
Cat. No.
ABIN334483
Quantity
100 μg
Datasheet
Datasheet
Reactivity
Human
Application
WB, ELISA, IF (cc), IF (p), IHC (fro), IHC (p), ICC
Validations
Cat. No.
ABIN1385221
Quantity
100 μL
Datasheet
Datasheet
Recommended RPGRIP1L ELISA试剂盒
Recommended RPGRIP1L 蛋白
Product
Reactivity
Source
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Source
Tobacco (Nicotiana tabacum)
Validations
Cat. No.
ABIN3092708
Quantity
1 mg
Datasheet
Datasheet
Reactivity
Mouse
Source
Tobacco (Nicotiana tabacum)
Validations
Cat. No.
ABIN3136445
Quantity
1 mg
Datasheet
Datasheet
Latest Publications for our RPGRIP1L Products
: "Superresolution Pattern Recognition Reveals the Architectural Map of the Ciliary Transition Zone." in: Scientific reports, Vol. 5, pp. 14096, (2015) (PubMed).: "CEP162 is an axoneme-recognition protein promoting ciliary transition zone assembly at the cilia base." in: Nature cell biology, Vol. 15, Issue 6, pp. 591-601, (2013) (PubMed).
: "Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome." in: Nature genetics, Vol. 39, Issue 7, pp. 882-8, (2007) (PubMed).
Synonyms and alternative names related to RPGRIP1L
RPGRIP1 like (RPGRIP1L), RPGRIP1-like (rpgrip1l), RPGRIP1 like (rpgrip1l), Protein fantom (mks-5), Rpgrip1-like (Rpgrip1l), RPGRIP1 like (Rpgrip1l), 1700047E16Rik, 4931437C01, cors3, CORS3, FTM, Ftm, jbts7, JBTS7, mks5, MKS5, nphp8, NPHP8, Nphp8, RGD1311099, si:ch1073-301i20.1Protein level used designations for RPGRIP1L
- RPGRIP1-like
- proteasome activator complex subunit 4
- protein fantom-like
- RPGR-interacting protein 1-like protein
- fantom homolog
- nephrocystin-8
- protein fantom
- RPGRIP1-like protein
- fantom
You are here:
