Anti-ROR2 antibody(DM174), Rabbit mAb DME100174
Specifications
| 10µg / 100µg / 500µg |
Background:
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.
Synonyms:
ROR2,NTRKR2
Clonality:
Monoclonal
Species reactivity:
Human
Host species:
Rabbit
Taraget:
ROR2
Isotype:
Rabbit IgG
Purification:
Purified from cell culture supernatant by affinity chromatography
Applications:
ELISA|Flow Cyt
Recommended dilution:
ELISA 1/5000-10000;Flow Cyt 1/100
Formulation:
Liquid
Precaution:
Research use only
More info:
Email: info@sobekbio.com
Orders:
Email: orders@sobekbio.com
