R Recombinant
Recombinant: Superior lot-to-lot consistency, continuous supply, and animal-free manufacturing.
RUNX2 (D1L7F) Rabbit mAb #12556
Filter:
- WB
- IP
- IF
- F
- ChIP
Supporting Data
| REACTIVITY | H M R |
| SENSITIVITY | Endogenous |
| MW (kDa) | 55-62 |
| Source/Isotype | Rabbit IgG |
Application Key:
- WB-Western Blotting
- IP-Immunoprecipitation
- IF-Immunofluorescence
- F-Flow Cytometry
- ChIP-Chromatin Immunoprecipitation
Species Cross-Reactivity Key:
- H-Human
- M-Mouse
- R-Rat
Product Information
Product Usage Information
For optimal ChIP and ChIP-seq results, use 5 μl of antibody and 10 μg of chromatin (approximately 4 x 106 cells) per IP. This antibody has been validated using SimpleChIP® Enzymatic Chromatin IP Kits.
| Application | Dilution |
|---|---|
| Western Blotting | 1:1000 |
| Immunoprecipitation | 1:50 |
| Immunofluorescence (Immunocytochemistry) | 1:6400 - 1:12800 |
| Flow Cytometry (Fixed/Permeabilized) | 1:1600 - 1:6400 |
| Chromatin IP | 1:100 |
| Chromatin IP-seq | 1:100 |
Storage
Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA, 50% glycerol and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody.
For a carrier free (BSA and azide free) version of this product see product #68007.
For a carrier free (BSA and azide free) version of this product see product #68007.
Protocol
Specificity / Sensitivity
RUNX2 (D1I7F) Rabbit mAb recognizes endogenous levels of total RUNX2 protein.
Species Reactivity:
Human, Mouse, Rat
Source / Purification
Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Ala273 of human RUNX2 protein.
Background
Runt-related transcription factor 2 (RUNX2) is a member of the RUNX family of transcription factors. It is involved in osteoblast differentiation and skeletal morphogenesis. RUNX2 regulates the transcription of various genes, including osteopontin, bone sialoprotein, and osteocalcin, via binding to the core site of the enhancers or promoters (1-3). RUNX2 is crucial for the maturation of osteoblasts and both intramembranous and endochondral ossification. Mutations in the corresponding RUNX2 gene have been associated with the bone development disorder cleidocranial dysplasia (CCD) (4-6). RUNX2 is also abnormally expressed in various human cancers, including prostate and breast cancer. It plays an important role in migration, invasion, and bone metastasis of prostate and breast cancer cells (7-10).
- Viereck, V. et al. (2002) J Cell Biochem 86, 348-56.
- Willis, D.M. et al. (2002) J Biol Chem 277, 37280-91.
- Tu, Q. et al. (2008) J Cell Physiol 217, 40-7.
- Quack, I. et al. (1999) Am J Hum Genet 65, 1268-78.
- Cardoso, B.M. et al. (2010) Clin Dysmorphol 19, 150-2.
- Han, M.S. et al. (2010) J Cell Biochem 110, 97-103.
- Akech, J. et al. (2010) Oncogene 29, 811-21.
- van der Deen, M. et al. (2010) J Cell Biochem 109, 828-37.
- Barnes, G.L. et al. (2003) Cancer Res 63, 2631-7.
- Barnes, G.L. et al. (2004) Cancer Res 64, 4506-13.
限制使用
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For Research Use Only. Not For Use In Diagnostic Procedures.
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