CPLANE1 Antibodies

AND CPLANE1 ELISA kits, CPLANE1 Proteins

Many biological assays use antibodies to detect CPLANE1, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with CPLANE1 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop CPLANE1 antibodies...

We validate the specificity of these antibodies to CPLANE1 by testing them on tissues known to express CPLANE1 positively and negatively. Browse below to find the CPLANE1 antibody that suites your experiment. We have 0 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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CPLANE1 Infographic by Boster Bio

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CPLANE1 Overview

Facts about Ciliogenesis and planar polarity effector 1.

Ciliogenesis and planar polarity effector 1 (CPLANE1)

Involved in ciliogenesis (PubMed:25877302). Involved in the establishment of cell polarity required for directional cell migration.

Proposed to behave in association with the CPLANE (ciliogenesis and planar polarity effectors) complicated. Involved in recruitment of peripheral IFT-A proteins to basal bodies (By similarity).

Gene Information

Human
Gene Name:	CPLANE1
Uniprot:	Q9H799
Entrez:	65250

Family

Belongs to:

No superfamily

Alternative Names

Ciliogenesis and planar polarity effector 1

Molecular Weight

Mass (kDA):
361.746 kDA

Genomic Context


Human

Location:	5p13.2
Sequence:	5; NC_000005.10 (37063928..37249499, complement)

Subcellular Localizations

Membrane; Multi-pass membrane protein. Cell projection, cilium. Localizes to the ciliary transition zone.

Diseases

Joubert syndrome 17 (JBTS17)

PTMs

Phosphoprotein

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/CPLANE1

References

PMID: 23012439 by Srour M., et al. Mutations in TMEM231 cause Joubert syndrome in French Canadians.

PMID: 24178751 by Lopez E., et al. C5orf42 is the major gene responsible for OFD syndrome type VI.