DFNA5 polyclonal, anti-human

Background:
Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene.

Synonyms: DFNA5, ICERE-1, non-syndromic hearing impairment protein 5

Cellular Location: Cytoplasm

Immunogen:
Recombinant protein of human DFNA5

Gene Symbol: DFNA5

Gene ID: 1687

Swiss prot: O60443

Calculated MW: 55kDa

Recommended dilution:
IHC 1:50-200

Purity:
Affinity purification

Storage Buffer:
Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.

Storage:
Store at -20°C. Avoid freeze / thaw cycles.