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.

Aliases：    NOV; NOVP; PLXN1; PLEXIN-A1    

Entrez GeneID：    5361    

Swissprot：    Q9UIW2      

WB Predicted band size：    211kDa    

Host/Isotype：    Mouse IgG1    

Species Reactivity：    Human    

Immunogen：    Purified recombinant fragment of human PLXNA1 (AA: 1100-1200) expressed in E. Coli.    

IF/ICC    1/100 - 1/500    

FCM    1/200 - 1/400    

ELISA    1/10000