PORIM Polyclonal Antibody, 100ul Fluorescent Staining Himmelfarb et al

Himmelfarb et al

This gene encodes a member of the Wiskott-Aldrich syndrome (WAS) protein family

Mutations in this gene have been associated with individuals affected by severe intellectual disability| early-onset epilepsy| microcephaly| congenital cataracts| growth retardation| and spasticity (PMID: 25439727)

|subcellular location:Translocates to mitochondria as an integral membrane protein

KLF1 encodes a hematopoietic-specific transcription factor that induces high-level expression of adult beta-globin and other erythroid genes

PORIM Polyclonal Antibody, 100ul Fluorescent Staining Himmelfarb et alThis gene encodes a highly glycosylated transmembrane protein with a high content of threonine and serine residues in its extracellular domain, similar to a broadly defined category of proteins termed mucins. Exposure of some cell types to anti PORIMIN (pro oncosis receptor inducing membrane injury) antibody, crosslinks this protein on the cell surface and induces a type of cell death termed oncosis. Oncosis is distinct from apoptosis and is