ROR2, Polyclonal, Invitrogen
Rabbit Polyclonal Antibody
Manufacturer: Invitrogen PA527991
The protein encoded by this gene is a receptor protein tyrosine kinase and type I transmembrane protein that belongs to the ROR subfamily of cell surface receptors. The protein may be involved in the early formation of the chondrocytes and may be required for cartilage and growth plate development. Mutations in this gene can cause brachydactyly type B, a skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In addition, mutations in this gene can cause the autosomal recessive form of Robinow syndrome, which is characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance.PA5-27991 targets ROR2 in WB applications and shows reactivity with Human samples.The PA5-27991 immunogen is recombinant fragment corresponding to a region within amino acids 353 and 664 of Human ROR2.
|Recombinant fragment corresponding to a region within amino acids 353 and 664 of Human ROR2|
|Antigen affinity chromatography|
|Store at -20°C, Avoid Freeze/Thaw Cycles|
|0.1M tris glycine with 10% glycerol and 0.01% thimerosal; pH 7|
|BDB, BDB1, NTRKR2, neurotrophic tyrosine kinase receptor-related 2, tyrosine-protein kinase transmembrane receptor ROR2|
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