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

is deleted in Williams-Beuren syndrome

An important paralog of this gene is S100A7A

N-terminal part of this PTP contains two tandem Src homolog (SH2) domains| which act as protein phospho-tyrosine binding domains| and mediate the interaction of this PTP with its substrates

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.