CCDC114 Antibodies

AND CCDC114 ELISA kits, CCDC114 Proteins

Many biological assays use antibodies to detect CCDC114, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with CCDC114 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop CCDC114 antibodies...

We validate the specificity of these antibodies to CCDC114 by testing them on tissues known to express CCDC114 positively and negatively. Browse below to find the CCDC114 antibody that suites your experiment. We have 1 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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CCDC114 Infographic by Boster Bio

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CCDC114 (NM_144577) Human Recombinant Protein

$813
Cat # PROTQ96M63
20 µg

CCDC114 Overview

Facts about Coiled-coil domain-containing protein 114.

CCDC114 3D structure. Source: alphafold

Coiled-coil domain-containing protein 114 (CCDC114)

Probable component of the outer dynein arm complex required along the whole axoneme for tethering of outer dynein arms. .

Gene Information

Human
Gene Name:	CCDC114
Uniprot:	Q96M63
Entrez:	93233

Family

Belongs to:

ODA1/DCC2 family

Alternative Names

coiled-coil domain containing 114; FLJ32926

Molecular Weight

Mass (kDA):
75.046 kDA

Genomic Context


Human

Location:	19q13.33
Sequence:	19; NC_000019.10 (48296452..48321971, complement)

Subcellular Localizations

Cell projection, cilium.

Diseases

Ciliary dyskinesia, primary, 20 (CILD20)

Interacting Proteins

C1orf216
CCDC151
HAUS1
HGS
KLC1

LNX1
TXN2

PTMs

Phosphoprotein

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/CCDC114

References

PMID: 23261303 by Onoufriadis A., et al. Splice-Site mutations in the axonemal outer dynein arm docking complex gene CCDC114 cause primary ciliary dyskinesia.

PMID: 23261302 by Knowles M.R., et al. Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesia.