BEAN1 Rabbit Polyclonal Antibody, 50ul sgRNA customized design loss of function mutations in

loss of function mutations in the encoded protein have been shown to cause nonsyndromic progressive hearing loss

May act as a motor required for the retrograde RAB6 regulated transport of Golgi membranes and associated vesicles along microtubules

and these opposite actions are thought to be mediated by two classes of receptors

Members of this family are believed to be involved in embryogenesis

immunocytochemistry

BEAN1 Rabbit Polyclonal Antibody, 50ul sgRNA customized design loss of function mutations in100 copies of pentanucleotide repeats including a (TGGAA)n sequence) are associated with spinocerebellar ataxia type 31. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.