
원본
Thermo Fisher Scientific ROR2 Monoclonal Antibody (OTI2G1), TrueMAB
상품 한눈에 보기
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.
- 카탈로그번호
- TA810049
- 판매단위
- pk
카탈로그
1개 옵션 · 카탈로그 번호를 클릭하면 복사됩니다회원가입 없이 바로 구매하세요
가입하지 않아도 비회원가로 구매하실 수 있습니다.
마지막 업데이트 2025. 08. 05. 오전 01:01
카탈로그 번호 · 상품 설명출고판매가담기
Thermo Fisher Scientific TA810049 ROR2 Monoclonal Antibody (OTI2G1), TrueMAB 100 ul pk판매 단위 pk ·
재고 확인 필요
600,200원VAT 포함 660,220원
Thermo Fisher Scientific · Thermo Fisher Scientific ROR2 Monoclonal Antibody (OTI2G1), TrueMAB
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.
Thermo Fisher Scientific 상품 둘러보기
전체보기문의
0개 · 배송·재고 문의는 실시간 상담이 빠릅니다아직 등록된 문의가 없어요.
