
Thermo Fisher Scientific Phospho-ROR2 (Ser449) Polyclonal Antibody
ROR2 단백질의 Ser449 인산화 형태를 특이적으로 검출하는 rabbit polyclonal antibody. Western blot에 최적화되어 있으며, 인간과 마우스 반응성. 액상 형태로 제공되며, PBS/glycerol buffer에 보관. 연구용으로만 사용 가능.
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Applications
Western Blot (WB)
- Tested Dilution: 1:1,000–1:3,000
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human, Mouse |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | A synthesized peptide derived from human ROR2 (Accession Q01974), corresponding to amino acid residues around phosphorylated Ser449 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Sequential chromatography |
| Storage Buffer | PBS, pH 7.4, with 50% glycerol |
| Contains | 0.02% sodium azide |
| Storage Conditions | -20°C |
| Shipping Conditions | Wet ice |
| RRID | AB_2817549 |
Product Specific Information
Antibody detects endogenous levels of ROR2 only when phosphorylated at Ser449.
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 plays a role in early chondrocyte formation, cartilage and growth plate development.
This protein is highly expressed during early embryonic development but decreases significantly after day 16, with very low levels in adult tissues.
Defects in ROR2 cause:
- 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, spinal defects, brachydactyly, and facial dysmorphism.
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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