ROR2 Rabbit Monoclonal Antibody (CAB5120)
- SKU:
- CAB5120
- Product Type:
- Antibody
- Reactivity:
- Mouse
- Host Species:
- Rabbit
- Isotype:
- IgG
- Research Area:
- Metabolism
Frequently bought together:
Description
Product Name: | ROR2 Rabbit Monoclonal Antibody |
SKU: | CAB5120 |
Size: | 20uL, 100uL |
Isotype: | IgG |
Host Species: | Rabbit |
Reactivity: | Mouse |
Immunogen: | A synthetic peptide corresponding to a sequence within amino acids 1-100 of human ROR2 (Q01974). |
Sequence: | MARG SALP RRPL LCIP AVWA AAAL LLSV SRTS GEVE VLDP NDPL GPLD GQDG PIPT LKGY FLNF LEPV NNIT IVQG QTAI LHCK VAGN PPPN VRWL KNDA |
Tested Applications: | WB ELISA |
Recommended Dilution: | WB,1:500 - 1:2000 |
Synonyms: | BDB; BDB1; NTRKR2; ROR2 |
Positive Sample: | Mouse liver,Mouse kidney |
Conjugate: | Unconjugated |
Cellular Localization: | Cell membrane, Single-pass type I membrane protein. |
Calculated MW: | 105kDa |
Observed MW: | 105kDa |
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.
Purification Method: | Affinity purification |
Gene ID: | 4920 |
Clone Number: | ARC1197 |
Storage Buffer: | Store at -20℃. Avoid freeze / thaw cycles.Buffer: PBS with 0.02% sodium azide,0.05% BSA,50% glycerol,pH7.3. |