Having trouble trying to find the right product? Chat with our scientists below - we're here to help!
Select a category to see relevant filters and products
2 results for "USH1C" in Products
USH1C Products
USH1C may be involved in protein-protein interaction. Defects in USH1C are the cause of Usher syndrome type 1c. It is an autosomal recessive sensory defect involving congenital profound sensorineural deafness, vestibular dysfunction, and blindness due to progressive retinitis pigmentosa. Defects in USH1C are also the cause of nonsyndromic recessive deafness.
Reactivity:
Human
Details:
Rabbit IgG Polyclonal
Applications:
IHC, WB, ELISA, IP
Reactivity:
Human
Details:
Rabbit IgG Monoclonal Clone #006
Applications:
ELISA