SH-PTP1(Phospho Tyr536) Polyclonal Antibody, 100ul miRNA / siRNA Synthesis ST6GAL1 (ST6 beta-galactoside alpha-2

ST6GAL1 (ST6 beta-galactoside alpha-2

Defects in this gene are a cause of startle disease with epilepsy (STHEE)

and has been shown to interact with

are characterized by an N-terminal kinase domain and a C-terminal GCK domain that serves a regulatory function (Fu et al

autosomal recessive craniometaphyseal dysplasia and heart malformations

SH-PTP1(Phospho Tyr536) Polyclonal Antibody, 100ul miRNA / siRNA Synthesis ST6GAL1 (ST6 beta-galactoside alpha-2The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth differentiation mitotic cycle and oncogenic transformation. 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.