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Mouse Monoclonal Antibody to ROR2
货号: 30623
别名: BDB; BDB1; NTRKR2
应用: FCM
反应种属: Human
抗体类型: Primary antibody
Swissprot: Q01974
规格:
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Description

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.

References

1. Int J Cancer. 2013 Aug 15;133(4):779-87.
2. Mol Cancer. 2010 Jun 30;9:170.

Specification

Aliases BDB; BDB1; NTRKR2
Entrez GeneID 4920
Swissprot Q01974
clone 6F2D10
WB Predicted band size 104.8kDa
Host/Isotype Mouse IgG1
Antibody Type Primary antibody
Storage Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Species Reactivity Human
Immunogen Purified recombinant fragment of human ROR2 (AA: 59-155) expressed in E. Coli.
Formulation Purified antibody in PBS with 0.05% sodium azide.

Application

FCM 1/200 - 1/400
ELISA 1/10000
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