Sensorineural Hearing Loss (SHL)
Sensorineural hearing loss (SNHL) is a type of hearing loss, or deafness, in which the root cause lies in the inner ear or sensory organ or the vestibulocochlear nerve or neural part. SNHL accounts for about 90% of hearing loss reported. SNHL may occurs as a consequence of damaged or deficient cochlear hair cell function. The hair cells may be abnormal at birth, or damaged during the lifetime of an individual. There are both external causes of damage, like noise trauma and infection, and intrinsic abnormalities, like deafness genes.
Studies showed that the BALB/c mouse strain as an animal model for the study of progressive sensorineural hearing loss, mice ranging in age from young adult through middle age were studied. Aspirin-induced hearing loss as a model of sensorineural hearing loss is with sensorineural deafness, and there are large individual differences in the amount of temporary hearing loss induced by fixed doses of aspirin.
Organism species: Pan-species (General)
|PRODUCT TYPE||CATALOG NO.||PRODUCT NAME||APPLICATIONS|
|Proteins||N/A||Recombinant Sensorineural Hearing Loss (SHL)||Antigenic Transformation Customized Service Offer|
|Antibodies||N/A||Monoclonal Antibody to Sensorineural Hearing Loss (SHL)||Monoclonal Antibody Customized Service Offer|
|N/A||Polyclonal Antibody to Sensorineural Hearing Loss (SHL)||Polyclonal Antibody Customized Service Offer|
|Assay Kits||N/A||CLIA Kit for Sensorineural Hearing Loss (SHL)||CLIA Kit Customized Service Offer|
|N/A||ELISA Kit for Sensorineural Hearing Loss (SHL)||ELISA Kit Customized Service Offer|