Function
Together with ARL2, plays a role in the nuclear translocation, retention and transcriptional activity of STAT3. May play a role as an effector of ARL2.
Biological Context
Subcellular Location: Cytoplasm; Mitochondrion intermembrane space; Cytoplasm, cytoskeleton, microtubule organizing center, centrosome; Nucleus; Cytoplasm, cytoskeleton, spindle; Cytoplasm, cytoskeleton, cilium basal body
Tissue Specificity: Expressed in retina pigment epithelial cells (at protein level). Widely expressed
Disease Association: Retinitis pigmentosa 82 with or without situs inversus (RP82) : An autosomal recessive disorder characterized by variable association of retinitis pigmentosa with situs inversus. Retinitis pigmentosa is characterized by retinal pigment deposits visible on fundus examination and primary loss of rod photoreceptor cells followed by secondary loss of cone photoreceptors. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well. Situs inversus is a congenital abnormality in which organs in the thorax and the abdomen are opposite to their normal positions due to lateral transposition. [The disease is caused by variants affecting the gene represented in this entry]
Product Specifications
Recombinant Human ADP-ribosylation factor-like protein 2-binding protein (ARL2BP) is a recombinant protein from Homo sapiens (Human), expressed in E.coli, covering amino acids 1-163aa, with N-terminal GST-tagged tag, molecular weight 45.8kDa, purity Greater than 90% as determined by SDS-PAGE.. Suitable for ELISA and Western Blot applications.
