Cynomolgus ROR2 Protein, N-His Tag
Description :Recombinant Cynomolgus ROR2 protein with N-terminal 10×His tagBackground : 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. Molecular Characterization: mass of 42.6 kDa after removal of the signal peptide. The apparent molecular mass of His-cROR2 is approximately 35-55 kDa due to glycosylation.Tag :N-10×His tag
Product Specifications
Product Name Alternative
BDB; BDB1; NTRKR2
UniProt
XP_005582291.2
Host
HEK293
Target Antigen
ROR2
Purification
The purity of the protein is greater than 85% as determined by SDS-PAGE and Coomassie blue staining.
Components
Lyophilized from sterile PBS, pH 7.4. Normally 5 % - 8% trehalose is added as protectants before lyophilization.
Storage Conditions
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