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The protein encoded by CEACAM16 is a secreted glycoprotein that in mouse interacts with tectorial membrane proteins in the inner ear. Additionally we are shipping CEACAM16 Kits (4) and CEACAM16 Proteins (3) and many more products for this protein.
Showing 10 out of 22 products:
Human Monoclonal CEACAM16 Primary Antibody for cELISA, FACS - ABIN1381739
Kammerer, Rüttiger, Riesenberg, Schäuble, Krupar, Kamp, Sunami, Eisenried, Hennenberg, Grunert, Bress, Battaglia, Schrewe, Knipper, Schneider, Zimmermann: Loss of mammal-specific tectorial membrane component carcinoembryonic antigen cell adhesion molecule 16 (CEACAM16) leads to hearing impairment at low and high frequencies. in The Journal of biological chemistry 2012
Show all 2 references for ABIN1381739
Dog (Canine) Polyclonal CEACAM16 Primary Antibody for WB - ABIN2782041
Zebhauser, Kammerer, Eisenried, McLellan, Moore, Zimmermann: Identification of a novel group of evolutionarily conserved members within the rapidly diverging murine Cea family. in Genomics 2005
Data indicate that a heterozygous missense mutation, c.505G>A (p.G169R) in exon 3 of the CEACAM16 gene (carcinoembryonic antigen-related cell adhesion molecule 16) was identified in autosomal dominant nonsyndromic hearing loss family.
CEACAM16 can probably form higher order structures with other tectorial membrane proteins such as alpha-tectorin (show TECTA Antibodies) and beta-tectorin (show TECTB Antibodies) and influences the physical properties of the tectorial membrane
data identify CEACAM16 as an alpha-tectorin-interacting protein that concentrates at the point of attachment of the TM to the stereocilia and, when mutated, results in ADNSHL at the DFNA4 locus
The data of this study indicated that CEACAM16 is required for striated (show NSDHL Antibodies)-sheet matrix formation. Its continual expression may stabilize the noncollagenous TM matrix.
The protein encoded by this gene is a secreted glycoprotein that in mouse interacts with tectorial membrane proteins in the inner ear. The encoded adhesion protein is found in cochlear outer hair cells and appears to be important for proper hearing over an extended frequency range. Defects in this gene likely are a cause of non-syndromic autosomal dominant hearing loss.
carcinoembryonic antigen-related cell adhesion molecule 16
, carcinoembryonic antigen like-2 protein
, chromosome 1 GSS clone AHTH152
, CEA-related cell adhesion molecule 16
, B-cell leukemia/lymphoma 3