PLXNA1 (Plexin A1) is a Protein Coding gene. Diseases associated with PLXNA1 include Hereditary Congenital Facial Paresis. Among its related pathways are Developmental Biology and Neuroscience. GO annotations related to this gene include receptor activity and semaphorin receptor activity. An important paralog of this gene is PLXNA3.
应用类型
FCM
免疫原
Purified recombinant fragment of human PLXNA1 (AA: 1100-1200) expressed in E. Coli.
