Description
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.

References
1.PLoS One. 2016 Mar 10;11(3):e0149833. 2.World J Gastroenterol. 2007 Dec 28;13(48):6558-61.

Specification
Aliases	NOV; NOVP; PLXN1; PLEXIN-A1
Entrez GeneID	5361
Swissprot	Q9UIW2
clone	7B8H9
WB Predicted band size	211kDa
Host/Isotype	Mouse IgG2b
Antibody Type	Primary antibody
Storage	Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Species Reactivity	Human
Immunogen	Purified recombinant fragment of human PLXNA1 (AA: 1100-1200) expressed in E. Coli.
Formulation	Purified antibody in PBS with 0.05% sodium azide

Application
FCM	1/200 - 1/400
ELISA	1/10000