Pejvakin / PJVK antibody

Principal name

Pejvakin / PJVK antibody

Alternative names for Pejvakin / PJVK antibody

DFNB59, Gm1001, Autosomal recessive deafness type 59 protein

SwissProt ID

Q0ZLH2 (Mouse), Q0ZLH3 (Human)

Gene ID

381375 (Dfnb59)

Available reactivities

Hu (Human), Ms (Mouse)

Available hosts


Available applications

Frozen Sections (C), Paraffin Sections (P), Western blot / Immunoblot (WB)

Background of Pejvakin / PJVK antibody

FUNCTION: Essential in the activity of auditory pathway neurons. DISEASE: 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. MISCELLANEOUS: 'Pejvak' means 'echo' in Persian.

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Catalog No.    

DFNB59 overexpression lysate

DFNB59 overexpression lysate  
0.1 mg / €280.00
  OriGene Technologies, Inc.

1 Item(s)

per page
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