Fish Polyclonal Antibody, 50ul Oligo Pool mitochondrial and other membranes) and

mitochondrial and other membranes) and a soluble form in erythrocytes

Defects in this gene cause Hailey-Hailey disease

a multiprotein complex that activates transcription by remodeling chromatin and mediating histone acetylation and deubiquitination

This gene is a member of the septin family of nucleotide binding proteins

member 1 (WNT) signaling pathway and can induce apoptosis

Fish Polyclonal Antibody, 50ul Oligo Pool mitochondrial and other membranes) andSH3PXD2A is also named as FISH, KIAA0418, SH3MD1, TKS5. SH3PXD2A contains an amino terminal PX domain followed by five SH3 domains. It is a cytoplasmic protein in normal fibroblasts (PMID: 19464300). The p140 and p130 forms of SH3PXD2A may be generated by other splice variations. The complexity of SH3PXD2A isoforms is also evident in different cell types. For example in human platelets a single band of 150kDa was detected, whereas all three forms were