ROR2 Rabbit Polyclonal Antibody (CAB5620)
- SKU:
- CAB5620
- Product Type:
- Antibody
- Reactivity:
- Human
- Mouse
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Metabolism
Frequently bought together:
Description
Product Name: | ROR2 Rabbit Polyclonal Antibody |
SKU: | CAB5620 |
Size: | 20uL, 100uL |
Isotype: | IgG |
Host Species: | Rabbit |
Reactivity: | Human,Mouse,Rat |
Immunogen: | A synthetic peptide corresponding to a sequence within amino acids 100-200 of human ROR2 (NP_004551.2). |
Sequence: | APVV QEPR RIII RKTE YGSR LRIQ DLDT TDTG YYQC VATN GMKT ITAT GVLF VRLG PTHS PNHN FQDD YHED GFCQ PYRG IACA RFIG NRTI YVDS LQMQ G |
Tested Applications: | WB IHC-P ELISA |
Recommended Dilution: | WB,1:500 - 1:1000 IHC-P,1:100 - 1:200 |
Synonyms: | BDB; BDB1; NTRKR2; ROR2 |
Positive Sample: | Mouse embryo |
Conjugate: | Unconjugated |
Cellular Localization: | Cell membrane, Single-pass type I membrane protein. |
Calculated MW: | 105kDa |
Observed MW: | 140kDa |
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 |
Storage Buffer: | Store at -20℃. Avoid freeze / thaw cycles.Buffer: PBS with 0.02% sodium azide,50% glycerol,pH7.3. |