MYO7A Antilichaam / Onconventionele Myosine-VIIa

Mutations in MYO7A are associated with hereditary hearing loss, Usher syndrome type 1B, and certain forms of retinitis pigmentosa. MYO7A is essential for maintaining stereocilia structure in cochlear hair cells and for transporting opsin-containing vesicles in retinal cells, highlighting its importance in sensory cell maintenance and signaling. Using a high-quality MYO7A antibody enables sensitive detection in applications such as western blot, immunohistochemistry, and immunofluorescence. An MYO7A antibody from NSJ Bioreagents provides consistent performance for research into sensory biology, genetic disorders, and intracellular transport mechanisms. Selecting the right MYO7A antibody is essential for achieving accurate and reproducible results.

Western blot: 1:500, Immunohistochemistry (FFPE) : 1:50

Q13402

Human, Mouse, Rat

A peptide sequence specific to Unconventional Myosin-VIIa was used as the immunogen for the MYO7A antibody.

AFCH-13

WB, IHC-P

Affinity chromatography

Purified

This MYO7A antibody is available for research use only.

After reconstitution, the MYO7A antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.

Antibody in PBS with 0.02% sodium azide, 50% glycerol and 0.4-0.5 mg/mL BSA

Optimal dilution of the MYO7A antibody should be determined by the researcher.

Cytoplasm

IHC staining of FFPE human lung cancer tissue with MYO7A antibody, HRP-secondary and DAB substrate. HIER: boil tissue sections in pH8 EDTA for 20 min and allow to cool before testing.