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Search Thermo Fisher Scientific
Reconstitute in 100 µL of sterile water. Centrifuge to remove any insoluble material.
The peptide is homologous in rat.
Specificity of this antibody: Pejvakin.
Essential in the activity of auditory pathway neurons. Defects in PJVK are the cause of non-syndromic sensorineural deafness autosomal recessive type 59 (DFNB59). DFNB59 is a form of sensorineural hearing impairment with absent or severely abnormal auditory brainstem response but normal otoacoustic emissions (auditory neuropathy or auditory dys-synchrony). Auditory neuropathies result from a lesion in the area including the inner hair cells, connections between the inner hair cells and the cochlear branch of the auditory nerve, the auditory nerve itself and auditory pathways of the brainstem. 'Pejvak' means 'echo' in Persian.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: autosomal recessive deafness type 59 protein homolog; deafness, autosomal recessive 59; DFNB59 deafness; Pejvakin; Protein sirtaki
Gene Aliases: Dfnb59; Gm1001; Pjvk
UniProt ID: (Mouse) Q0ZLH2
Entrez Gene ID: (Mouse) 381375, (Rat) 679552
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