epitope corresponding to amino acids 1-133 representing full length NORRIN of human origin
Modification Notes
The NDP (Norrie disease protein) gene encodes the secreted NORRIN protein. Mutations in this gene lead to Norrie disease, a rare X-linked disorder characterized by congenital blindness, deafness and mental retardation. X-linked familial exudative vitreoretinopathy (XL-FEVR), an ocular disorder characterized by a failure of peripheral retinal vascularization, is also associated with mutations in the NDP gene. NORRIN utilizes the Wnt/Frizzled signaling pathway and plays a role in vascular development. Research indicates that it induces growth of ocular capillaries and that pharmacologic regulation of NORRIN may be useful for treatment of the vascular abnormalities associated with Norrie disease or other vascular disorders of the retina.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFELISA
recommended for detection of NORRIN of mouse, rat and human origin by WB, IP, IF and ELISA also reactive with additional species, including equine, canine, bovine, porcine and avian:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope corresponding to amino acids 1-133 representing full length NORRIN of human origin
Tissue Specificity
epitope corresponding to amino acids 1-133 representing full length NORRIN of human origin
recommended for detection of NORRIN of mouse, rat and human origin by WB, IP, IF and ELISA also reactive with additional species, including equine, canine, bovine, porcine and avian:
Additional Information
Form
Liquid
Storage Instructions
For short-term storage, store at 4° C. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.