CacheBy
Thermo Fisher Scientific ROR2 Monoclonal Antibody (OTI5F8), TrueMAB
원본

Thermo Fisher Scientific ROR2 Monoclonal Antibody (OTI5F8), TrueMAB

상품 한눈에 보기

ROR2 단백질을 인식하는 Mouse monoclonal 항체로, Western blot 및 IHC(P)에서 검증됨. Human ROR2(aa 796-927) 항원으로 제작. 동결건조 형태, 1 mg/mL 농도. 연구용으로만 사용 가능.

판매단위
pk
카탈로그 보기

카탈로그

1개 옵션
회원가입 없이 바로 구매하세요
가입하지 않아도 비회원가로 구매하실 수 있습니다.
마지막 업데이트 2025. 08. 03. 오전 08:25
Thermo Fisher Scientific CF810009 ROR2 Monoclonal Antibody (OTI5F8), TrueMAB 100 ug pk판매 단위 pk ·
재고 확인 필요
815,400원VAT 포함 896,940원

Thermo Fisher Scientific · Thermo Fisher Scientific ROR2 Monoclonal Antibody (OTI5F8), TrueMAB

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:500
Immunohistochemistry (Paraffin) (IHC (P)) 1:250

Product Specifications

항목 내용
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone OTI5F8
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 of distilled water to obtain a final antibody concentration of approximately 1 mg/mL.
For conjugation experiments, perform an additional desalting step (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 plays a role in early chondrocyte formation, cartilage, and growth plate development.
This protein is highly expressed during early embryogenesis, decreases significantly by day 16, and is minimally expressed in adult tissues.

Mutations in ROR2 are associated with:

  • Brachydactyly type B1 (BDB1): Autosomal dominant skeletal disorder with hypoplasia/aplasia of distal phalanges and nails, affecting both fingers and toes.
  • Robinow syndrome (RRS): Autosomal recessive disorder characterized by skeletal dysplasia, limb shortening, spinal defects, and distinctive facial features.

The protein includes:

  • 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

전체보기

문의

0

아직 등록된 문의가 없어요.