MYO7A Polyclonal Antibody

Reddot Biotech

MYO7A Polyclonal Antibody

5

ELISA, ImmunoHistoChemistry

Research Use Only

Polyclonal

0.6 mg/ml

Unconjugated

MYO7A

myosin VIIA

DFNA11; DFNB2; myosin VIIA (Usher syndrome 1B (autosomal recessive, severe)); MYOVIIA; MYU7A; NSRD2; unconventional myosin-VIIa; USH1B

Rabbit

IgG

This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants.

Human, Mouse

-20°C

12352203