
Thermo Fisher Scientific ROR2 Monoclonal Antibody (OTI5E3), TrueMAB
ROR2 단백질을 인식하는 Mouse monoclonal antibody로 Western blot에 최적화됨. Human ROR2(aa 796-927) 항원을 기반으로 제작. 동결건조 형태이며 재구성 후 1 mg/mL 농도로 사용 가능. 연구용으로만 사용.
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Applications
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:500 |
Product Specifications
| 항목 | 내용 |
|---|---|
| Host / Isotype | Mouse / IgG1 |
| Class | Monoclonal |
| Type | Antibody |
| Clone | OTI5E3 |
| Immunogen | Human recombinant protein fragment corresponding to amino acids 796–927 of human ROR2 produced in E. coli |
| Conjugate | Unconjugated |
| Form | Lyophilized |
| Concentration | 1 mg/mL |
| Storage Conditions | -20°C, Avoid Freeze/Thaw Cycles |
| Shipping Conditions | Ambient (domestic); Wet ice (international) |
Product Specific Information
For reconstitution, add 100 µL distilled water to achieve a final antibody concentration of approximately 1 mg/mL.
For conjugation experiments, perform an additional desalting step (e.g., Zeba Spin Desalting Columns, 7K MWCO, 0.5 mL, Product #89882).
Target Information
ROR2 (receptor tyrosine kinase-like orphan receptor 2) is a type I transmembrane protein belonging to the ROR subfamily of cell surface receptors.
It is involved in early chondrocyte and cartilage formation and growth plate development. Expression is high during early embryonic development, decreasing significantly by day 16 and remaining low in adult tissues.
Defects in ROR2 are associated with:
- Brachydactyly type B1 (BDB1): Autosomal dominant skeletal disorder with hypoplasia/aplasia of distal phalanges and nails.
- Robinow syndrome (RRS): Autosomal recessive disorder characterized by skeletal dysplasia, limb bone shortening, spine defects, brachydactyly, and facial dysmorphism.
The ROR2 protein contains:
- 1 frizzled (FZ) domain
- 1 immunoglobulin-like C2-type domain
- 1 kringle domain
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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