ROBO3 Polyclonal Antibody

Rs. 16,500.00
SKU E-AB-15361

Overview

Synonyms FLJ21044,HGPPS,HGPS,RB inhibiting gene 1,Rbig 1,Rbig1,Retinoblastoma inhibiting gene 1,Rig 1,Rig1,Robo 3,Robo3,Robo3 protein,ROBO3,Roundabout axon guidance receptor homolog 3,Roundabout homolog 3,Roundabout like protein 3,Roundabout,axon guidance receptor,homolog 3 (Drosophila),Roundabout-like protein 3
Swissprot Q96MS0
Source Rabbit
Reactivity Human,Mouse
Immunogen Recombinant protein of human ROBO3
Application IHC,ELISA
Recommended dilution IHC 1:25-1:100
Concentration 0.4mg/mL
Clonality Polyclonal

Properties

Cellular localization  
Tissue specificity  
Isotype IgG
Purification Affinity purification
Conjugation Unconjugated
Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
Storage buffer PBS with 0.05% sodium azide, 50% glycerol, PH7.3
Background This gene is a member of the Roundabout (ROBO) gene family that controls neurite outgrowth, growth cone guidance, and axon fasciculation. ROBO proteins are a subfamily of the immunoglobulin transmembrane receptor superfamily. SLIT proteins 1-3, a family of secreted chemorepellants, are ligands for ROBO proteins and SLIT/ROBO interactions regulate myogenesis, leukocyte migration, kidney morphogenesis, angiogenesis, and vasculogenesis in addition to neurogenesis. This gene, ROBO3, has a putative extracellular domain with five immunoglobulin (Ig)-like loops and three fibronectin (Fn) type III motifs, a transmembrane segment, and a cytoplasmic tail with three conserved signaling motifs: CC0, CC2, and CC3 (CC for conserved cytoplasmic). Unlike other ROBO family members, ROBO3 lacks motif CC1. The ROBO3 gene regulates axonal navigation at the ventral midline of the neural tube. In mouse, loss of Robo3 results in a complete failure of commissural axons to cross the midline throughout the spinal cord and the hindbrain. Mutations ROBO3 result in horizontal gaze palsy with progressive scoliosis (HGPPS); an autosomal recessive disorder characterized by congenital absence of horizontal gaze, progressive scoliosis, and failure of the corticospinal and somatosensory axon tracts to cross the midline in the medulla. Alternative transcript variants have been described but have not been experimentally validated. 

 

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