Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
The protein encoded by OTOA is specifically expressed in the inner ear, and is located at the interface between the apical surface of the inner ear sensory epithelia and their overlying acellular gels. Additionally we are shipping OTOA Proteins (4) and OTOA Kits (1) and many more products for this protein.
Showing 10 out of 36 products:
Mouse (Murine) Polyclonal OTOA Primary Antibody for IHC (p), WB - ABIN655100
Shahin, Walsh, Rayyan, Lee, Higgins, Dickel, Lewis, Thompson, Baker, Nord, Stray, Gurwitz, Avraham, King, Kanaan: Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families. in European journal of human genetics : EJHG 2010
Show all 3 references for ABIN655100
Human Polyclonal OTOA Primary Antibody for EIA, IHC (p) - ABIN953947
Zwaenepoel, Mustapha, Leibovici, Verpy, Goodyear, Liu, Nouaille, Nance, Kanaan, Avraham, Tekaia, Loiselet, Lathrop, Richardson, Petit: Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22. in Proceedings of the National Academy of Sciences of the United States of America 2002
Show all 2 references for ABIN953947
A description of two novel OTOA mutations that were discovered in three consanguineous Pakistani families segregating autosomal recessive non-syndromic hearing impairment.
Large deletions in OTOA gene is associated with hearing loss.
Otoancorin is defective in autosomal recessive deafness DFNB22
The protein encoded by this gene is specifically expressed in the inner ear, and is located at the interface between the apical surface of the inner ear sensory epithelia and their overlying acellular gels. It is prposed that this protein is involved in the attachment of the inner ear acellular gels to the apical surface of the underlying nonsensory cells. Mutations in this gene are associated with autosomal recessive deafness type 22 (DFNB22). Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
, cancer/testis antigen 108