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:
目录价
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Description |
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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 |
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1. Int J Cancer. 2013 Aug 15;133(4):779-87. 2. Mol Cancer. 2010 Jun 30;9:170. |
Specification |
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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 |
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FCM | 1/200 - 1/400 |
ELISA | 1/10000 |