Function
May regulate MCM3AP phosphorylation through phosphatase recruitment. May act as a negative regulator of ABCB1 expression and function through the dephosphorylation of ABCB1 by TFPI2/PPP2R3C complex. May play a role in the activation-induced cell death of B-cells.
Biological Context
Subcellular Location: Nucleus; Cytoplasm
Tissue Specificity: Ubiquitously expressed in brain and other tissues
Disease Association: Myoectodermal gonadal dysgenesis syndrome (MEGD) : An autosomal recessive disorder characterized by 46,XY complete gonadal dysgenesis and extragonadal anomalies, including typical facial gestalt, low birth weight, myopathy, rod and cone dystrophy, anal atresia, omphalocele, sensorineural hearing loss, dry and scaly skin, skeletal abnormalities, renal agenesis and neuromotor delay. [The disease is caused by variants affecting the gene represented in this entry] | Spermatogenic failure 36 (SPGF36) : An autosomal dominant infertility disorder due to teratozoospermia, with spermatozoa showing anomalies of the head, acrosome, and nucleus. [The disease may be caused by variants affecting the gene represented in this entry]
Product Specifications
Recombinant Human Serine/threonine-protein phosphatase 2A regulatory subunit B' subunit gamma (PPP2R3C) is a recombinant protein from Homo sapiens (Human), expressed in E.coli, covering amino acids 1-453aa, with C-terminal 6xHis-tagged tag, molecular weight 60.2kDa, purity Greater than 90% as determined by SDS-PAGE.. Suitable for ELISA and Western Blot applications. Explore more Enzyme proteins →
