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RUNX2 is a member of the RUNX family of transcription factors and encodes a nuclear protein with an Runt DNA-binding domain. Additionally we are shipping RUNX2 Kits (36) and RUNX2 Proteins (12) and many more products for this protein.
Showing 10 out of 235 products:
Human Polyclonal RUNX2 Primary Antibody for DB - ABIN389942
McNamara, Sjöström, Burgess, Kim, Liu, Gordonov, Moghe, Meek, Oreffo, Su, Dalby: Skeletal stem cell physiology on functionally distinct titania nanotopographies. in Biomaterials 2011
Show all 8 references for ABIN389942
Human Polyclonal RUNX2 Primary Antibody for EIA - ABIN358487
Ermakov, Malkin, Keter, Kobyliansky, Livshits: Family-based association study of polymorphisms in the RUNX2 locus with hand bone length and hand BMD. in Annals of human genetics 2008
Show all 3 references for ABIN358487
Cow (Bovine) Polyclonal RUNX2 Primary Antibody for WB - ABIN2774905
Guo, Chung, Yang, Karsenty, Bringhurst, Kronenberg: PTH/PTHrP receptor delays chondrocyte hypertrophy via both Runx2-dependent and -independent pathways. in Developmental biology 2006
Show all 2 references for ABIN2774905
Human Polyclonal RUNX2 Primary Antibody for EIA, WB - ABIN360019
Rich, Rosová, Nolta, Myckatyn, Sandell, McAlinden: Upregulation of Runx2 and Osterix during in vitro chondrogenesis of human adipose-derived stromal cells. in Biochemical and biophysical research communications 2008
Show all 2 references for ABIN360019
Human Polyclonal RUNX2 Primary Antibody for WB - ABIN2780588
Lee, Lee, Ryoo, Park, Park, Bae, Cho, Park: The odontogenic ameloblast-associated protein (ODAM) cooperates with RUNX2 and modulates enamel mineralization via regulation of MMP-20. in Journal of cellular biochemistry 2010
Show all 2 references for ABIN2780588
Chicken Polyclonal RUNX2 Primary Antibody for WB - ABIN2774906
Ducy, Zhang, Geoffroy, Ridall, Karsenty: Osf2/Cbfa1: a transcriptional activator of osteoblast differentiation. in Cell 1997
Runx2 may have an evolutionarily conserved role in axis formation
In a model of instability-induced osteoarthritis, Runx2 was overexpressed in articular chondrocytes and osteophyte-forming cells in LOX-1 (show OLR1 Antibodies)(+)/(+) mice and was significantly downregulated in articular chondrocytes and osteophyte-forming cells in LOX-1 (show OLR1 Antibodies)(-)/(-) mice.
miR23b inhibits BMP9induced C2C12 myoblast osteogenesis via targeting of the Runx2 gene, acting as a suppressor.
Runx2-modified adipose-derived stem cells promote tendon graft integration in anterior cruciate ligament reconstruction.
FHL2 (show FHL2 Antibodies) might interact with Runx2 to mediate mesenchymal cell differentiation at the early stages of tooth development and human dental pulp cell differentiation.
our studies reveal a novel function for Runx2 in regulating mammary epithelial cell regenerative potential, possibly acting as a downstream target of WNT (show WNT2 Antibodies) signalling.
MED23 (show MED23 Antibodies) binds to RUNX2 and modulates its transcriptional activity.
Hand1 (show HAND1 Antibodies) downregulated Ihh (show IHH Antibodies) gene expression in vitro by inhibiting Runx2 transactivation of the Ihh (show IHH Antibodies) proximal promoter.
increased intranuclear actin forces MSC (show MSC Antibodies) into osteogenic lineage through controlling Runx2 activity; this process may be useful for clinical objectives of forming bone.
We observed that tranilast increased mRNA expression of both Sox9 (show SOX9 Antibodies) and Runx2 in differentiating ATDC5 chondrogenic progenitor cells.
Results propose that Utx (show KDM6A Antibodies) plays important roles in osteoblast differentiation by controlling the expressions of Runx2 and Osterix (show SP7 Antibodies).
downregulation of miR (show MLXIP Antibodies)-218 may contribute to the chemoresistance of non-small cell lung cancer cells to cisplatin, which leads to upregulation of RUNX2
miR (show MLXIP Antibodies)-30a play a role in suppressing proliferation, migration, and invasion of OS by targeting Runx2.
our results suggest that miR (show MLXIP Antibodies)-30a plays an important role to inhibit the proliferation of CS cells and presents a novel mechanism for direct miRNA-mediated suppression of Runx2 in CS.
the BMP-2 (show BMP2 Antibodies)/Smad1 (show GARS Antibodies)/5/RUNX2 signaling pathway participates in the silicon-mediated induction of COL-1 and osteocalcin (show BGLAP Antibodies) synth
Preameloblast-Derived Factors Mediate Osteoblast Differentiation of Human Bone Marrow Mesenchymal Stem Cells by Runx2-Osterix (show SP7 Antibodies)-BSP (show KLK6 Antibodies) Signaling.
Runx2 activation by BMP signaling mediates serum deprivation triggers upregulation of hST3Gal V gene expression in MG-63 cells.
GnRH (show GNRH1 Antibodies) regulates trophoblast invasion via RUNX2-mediated MMP2 (show MMP2 Antibodies)/MMP9 (show MMP9 Antibodies) expression.
An osteogenic medium is required for the differentiation of adul tmesenchymal stem cells, which is also under RUNX2 regulation. These findings are potentially valuable for clinical practice.
This integrative genomic study confirmed the role of RUNX2 as a potential driver of AS and identified a new AS susceptibility gene, CACNA1C (show CACNA1C Antibodies), belonging to the calcium signaling pathway.
The OPG (show TNFSF11 Antibodies) expression levels decreased while those of RANKL (show TNFSF11 Antibodies) and RUNX2 increased during orthodontic tooth movement, which suggested that they play a role in the osteogenesis process and the reconstruction of periodontal tissue.
These data also indicate that MGP (show MGP Antibodies) is under dual regulation by runx2 through the use of various isoforms and context-dependent formation of transcriptional complexes.
This gene is a member of the RUNX family of transcription factors and encodes a nuclear protein with an Runt DNA-binding domain. This protein is essential for osteoblastic differentiation and skeletal morphogenesis and acts as a scaffold for nucleic acids and regulatory factors involved in skeletal gene expression. The protein can bind DNA both as a monomer or, with more affinity, as a subunit of a heterodimeric complex. Mutations in this gene have been associated with the bone development disorder cleidocranial dysplasia (CCD). Transcript variants that encode different protein isoforms result from the use of alternate promoters as well as alternate splicing.
runt-related transcription factor 2
, transcription factor Runx2a
, transcription factor Cbfa1
, runt-related transcription factor 2-like
, AKV core binding factor
, PEA2-alpha A
, PEBP2 alpha A
, SL3-3 enhancer factor 1 alpha A subunit
, acute myeloid leukemia 3 protein
, core binding factor alpha 1
, osteoblast-specific transcription factor 2
, polyomavirus enhancer-binding protein 2 alpha A subunit
, runt domain, alpha subunit 1
, PEBP2-alpha A
, SL3/AKV core-binding factor alpha A subunit
, core-binding factor, runt domain, alpha subunit 1
, oncogene AML-3
, runt-related factor 2
, core-binding factor subunit alpha-1
, runt related transcription factor 2
, Runx2 spliced isoform
, runt-related transcription factor 2 type I
, runt-related transcription factor 2 type II
, core binding factor alpha 1 subunit