
Thermo Fisher Scientific ROR2 Monoclonal Antibody (OTI2G1), TrueMAB
ROR2 단백질을 인식하는 마우스 단클론 항체로 Western blot 및 IHC(P) 분석에 적합. 인간 시료 반응성. 고순도 친화 크로마토그래피 정제. -20°C 보관, 반복 동결 해동 피해야 함. 연구용으로만 사용.
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Applications and Tested Dilutions
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:500 |
| Immunohistochemistry (Paraffin) (IHC (P)) | 1:250 |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Mouse / IgG1 |
| Class | Monoclonal |
| Type | Antibody |
| Clone | OTI2G1 |
| Immunogen | Human recombinant protein fragment corresponding to amino acids 796–927 of human ROR2 produced in E. coli. |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Affinity chromatography |
| Storage Buffer | PBS with 1% BSA, 50% glycerol |
| Contains | 0.02% sodium azide |
| Storage Conditions | -20°C, Avoid Freeze/Thaw Cycles |
| Shipping Conditions | Ambient (domestic); Wet ice (international) |
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 formation, cartilage, and growth plate development. ROR2 is highly expressed during early embryonic development, with expression decreasing significantly by day 16 and remaining low in adult tissues.
Defects in ROR2 are associated with:
- Brachydactyly type B1 (BDB1): An autosomal dominant skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. Both fingers and toes are affected, with deformities in thumbs and big toes.
- Recessive Robinow syndrome (RRS): An autosomal disorder causing skeletal dysplasia, limb bone shortening, spinal defects, brachydactyly, and facial dysmorphia.
The 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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