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DFNB59

  • Official Full Name

    deafness, autosomal recessive 59

  • 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
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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