DFNB59
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Official Full Name
deafness, autosomal recessive 59
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Overview
The protein encoded by this gene is a member of the gasdermin family, a family which is found only in vertebrates. The encoded protein is required for the proper function of auditory pathway neurons. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal recessive type 59 (DFNB59). -
Synonyms
DFNB59; deafness, autosomal recessive 59; pejvakin; autosomal recessive deafness type 59 protein; PJVK;
Species | Cat.# | Product name | Source (Host) | Tag | Protein Length | Price |
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Human | DFNB59-977H | Recombinant Human DFNB59 | Mammalian Cell | His | ||
Human | DFNB59-2794H | Recombinant Human DFNB59 Protein, His (Fc)-Avi-tagged | HEK293 | His (Fc)-Avi | ||
Human | DFNB59-2794H-B | Recombinant Human DFNB59 Protein Pre-coupled Magnetic Beads | HEK293 |
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