Human USH1G ELISA Kit (HUFI05769)

The Human USH1G ELISA Kit from Assay Genie provides quantitative measurement of the USH1G protein, also known as SANS (scaffold protein containing ankyrin repeats and SAM domain), in human research samples. USH1G is a key gene implicated in Usher syndrome type 1, an autosomal recessive disorder that combines congenital sensorineural deafness with progressive retinitis pigmentosa, making this assay relevant to studies of inner ear hair cell function, photoreceptor degeneration, and rare-disease biomarker discovery.

Intended for research use only, the kit contains a pre-coated microplate, biotinylated detection antibody, recombinant standard, streptavidin-HRP conjugate, wash buffer, substrate, and stop solution. Each well accommodates 100 µL of sample, and the workflow supports plate-reader quantification following incubation and wash steps. Unopened kit components should be stored refrigerated at 4°C, protected from light, while reconstituted standards and concentrated detection antibody should be aliquoted and kept frozen to limit freeze-thaw cycles.

This format supports gene expression correlation studies, patient stratification work, and translational investigations into ciliopathies linked to the Usher protein interactome. Investigators studying hearing loss genetics, vision science, and sensory neuropathy can integrate the assay into broader panels measuring ciliary and synaptic proteins associated with hereditary sensory deficits.