Tissue expression
Cell line expression
Protein structure
ROR2
Receptor tyrosine kinase like orphan receptor 2BDB, BDB1, NTRKR2
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. [provided by RefSeq, Jul 2008]
Top validated antibodies |
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antibodies-online | ABIN2841812 | 7 references | Polyclonal |
WB
IHC
FC
|
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Abnova Corporation | PAB3385 | 3 references | Polyclonal |
WB
IHC
FC
|
|
OriGene | TA307281 | 1 references | Monoclonal |
WB
IHC
FC
|
|
NovoPro Bioscience Inc. | 130914 | Polyclonal |
WB
EL
IHC
FC |
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Abgent | AP7672A | Polyclonal |
WB
IHC
FC
|
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Supportive data in Antibodypedia
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Supportive data in Antibodypedia
Data presented on provider website
Data in Antibodypedia (inconclusive)
Recommended by provider