
Thermo Fisher Scientific RUNX2 Recombinant Rabbit Monoclonal Antibody (6H4L27)
RUNX2 단백질을 인식하는 재조합 토끼 모노클로날 항체로, 인간 시료에 반응하며 WB에 적합합니다. 높은 특이성과 감도를 제공하며 로트 간 일관성이 뛰어납니다. 단기 4°C, 장기 -20°C 보관 권장.
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Applications
Western Blot (WB)
- Tested Dilution: 1:200–1:1,000
- View 1 publication
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Published Species | Human |
| Host / Isotype | Rabbit / IgG |
| Expression System | Expi293 |
| Class | Recombinant Monoclonal |
| Type | Antibody |
| Clone | 6H4L27 |
| Immunogen | Protein corresponding to human RUNX2 (aa235–aa400) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.5 mg/mL |
| Purification | Protein A |
| Storage Buffer | PBS, pH 7.4 |
| Contains | 0.09% sodium azide |
| Storage Conditions | Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. |
| Shipping Conditions | Wet ice |
| RRID | AB_2725282 |
Additional Formats
Product Specific Information
This antibody is predicted to react with Monkey, Pig, Mouse, and Rat.
Recombinant rabbit monoclonal antibodies are produced using in vitro expression systems. These systems clone specific antibody DNA sequences from immunoreactive rabbits and screen individual clones to select the best candidates for production.
Advantages include:
- Better specificity and sensitivity
- Lot-to-lot consistency
- Animal origin-free formulations
- Broader immunoreactivity due to larger rabbit immune repertoire
Target Information
RUNX2 is a nuclear protein and a member of the RUNX family of transcription factors containing a Runt DNA-binding domain. It is essential for membranous and endochondral bone formation, regulating osteoblastic differentiation and skeletal morphogenesis. RUNX2 acts as a scaffold for nucleic acids and regulatory factors involved in skeletal gene expression.
It binds DNA as a monomer or more strongly as part of a heterodimeric complex. RUNX2 enhances TGFBR1 expression in osteoblasts and cooperates with DLX5 or related factors to activate osteoblast-specific gene expression.
Mutations in RUNX2 can lead to bone development disorders such as cleidocranial dysplasia (CCD).
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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