CacheBy
Thermo Fisher Scientific RUNX2 Polyclonal Antibody
원본

Thermo Fisher Scientific RUNX2 Polyclonal Antibody

상품 한눈에 보기

RUNX2 단백질을 인식하는 염소 유래 폴리클로날 항체로, Western blot 및 IHC에 사용 가능. 인간, 마우스, 랫트에 반응하며, 골형성 및 골아세포 분화 연구에 적합. 동결건조 형태로 제공되며 장기 보관 시 -20°C 권장.

판매단위
pk
카탈로그 보기

카탈로그

1개 옵션
회원가입 없이 바로 구매하세요
가입하지 않아도 비회원가로 구매하실 수 있습니다.
마지막 업데이트 2025. 08. 04. 오후 11:11
Thermo Fisher Scientific OSR00350W-100UL RUNX2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
542,600원VAT 포함 596,860원

Thermo Fisher Scientific · Thermo Fisher Scientific RUNX2 Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution Publications
Western Blot (WB) 1:300–1:2,000 -
Immunohistochemistry (IHC) 1:300–1:2,000 -
Miscellaneous PubMed (Misc) - View 1 publication

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Published Species Not Applicable
Host / Isotype Goat / Ig
Class Polyclonal
Type Antibody
Immunogen A synthetic peptide from internal region of mouse Runx2 conjugated to blue carrier protein
Conjugate Unconjugated
Form Lyophilized
Concentration Not Determined
Storage Buffer Whole serum
Contains No preservative
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. Glycerol (1:1) may be added for added stability.
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

  • Reconstitute in 100 µL of sterile water. Centrifuge to remove any insoluble material.
  • The peptide is homologous in human and rat.
  • Specificity: Runx2.

Target Information

RUNX2 is a nuclear transcription factor belonging to the RUNX family, containing a Runt DNA-binding domain. It is essential for both membranous and endochondral bone formation, regulating osteoblastic differentiation and skeletal morphogenesis. RUNX2 also functions as a scaffold for nucleic acids and regulatory factors involved in skeletal gene expression. It binds DNA as a monomer or as part of a heterodimeric complex, enhancing TGFBR1 expression in osteoblasts and cooperating with DLX5 or related factors to activate osteoblast-specific genes. Mutations in RUNX2 are associated with cleidocranial dysplasia (CCD).


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.