Runt Related Transcription Factor 2 (RUNX2)

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AML3; CBFA1; CCD1; OSF2; PEBP2A; Acute myeloid leukemia 3 ; Core-binding factor alpha-1; Osteoblast-specific transcription factor 2; Polyomavirus enhancer-binding protein 2 A

Runt Related Transcription Factor 2 (RUNX2)

Cbfa1/Runx2 is a key transcription factor associated with osteoblast differentiation.This protein is a member of the RUNX family of transcription factors and has a Runt DNA-binding domain. It 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. Transcript variants of the gene that encode different protein isoforms result from the use of alternate promoters as well as alternate splicing.The RUNX2 transcription factor is the master regulator of osteoblast differentiation is required for chondrocyte hypertrophy .

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins RPB011Hu01 Recombinant Runt Related Transcription Factor 2 (RUNX2) Positive Control; Immunogen; SDS-PAGE; WB.
Antibodies PAB011Hu01 Polyclonal Antibody to Runt Related Transcription Factor 2 (RUNX2) WB; IHC; ICC; IP.
MAB011Hu22 Monoclonal Antibody to Runt Related Transcription Factor 2 (RUNX2) WB; IHC; ICC; IP.
Assay Kits SEB011Hu ELISA Kit for Runt Related Transcription Factor 2 (RUNX2) Enzyme-linked immunosorbent assay for Antigen Detection.

Organism species: Mus musculus (Mouse)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins RPB011Mu01 Recombinant Runt Related Transcription Factor 2 (RUNX2) Positive Control; Immunogen; SDS-PAGE; WB.
RPB011Mu02 Recombinant Runt Related Transcription Factor 2 (RUNX2) Positive Control; Immunogen; SDS-PAGE; WB.
Antibodies PAB011Mu01 Polyclonal Antibody to Runt Related Transcription Factor 2 (RUNX2) WB; IHC; ICC; IP.
PAB011Mu02 Polyclonal Antibody to Runt Related Transcription Factor 2 (RUNX2) WB; IHC; ICC; IP.
LAB011Mu81 FITC-Linked Polyclonal Antibody to Runt Related Transcription Factor 2 (RUNX2) WB; IHC; ICC; IF.
Assay Kits SEB011Mu ELISA Kit for Runt Related Transcription Factor 2 (RUNX2) Enzyme-linked immunosorbent assay for Antigen Detection.

Organism species: Rattus norvegicus (Rat)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Runt Related Transcription Factor 2 (RUNX2) Recombinant Protein Customized Service Offer
Antibodies PAB011Ra01 Polyclonal Antibody to Runt Related Transcription Factor 2 (RUNX2) WB; IHC; ICC; IP.
Assay Kits n/a CLIA Kit for Runt Related Transcription Factor 2 (RUNX2) CLIA Kit Customized Service Offer
n/a ELISA Kit for Runt Related Transcription Factor 2 (RUNX2) ELISA Kit Customized Service Offer

Organism species: Cavia (Guinea pig )

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Runt Related Transcription Factor 2 (RUNX2) Recombinant Protein Customized Service Offer
Antibodies PAB011Gu01 Polyclonal Antibody to Runt Related Transcription Factor 2 (RUNX2) WB; IHC; ICC; IP.
Assay Kits n/a CLIA Kit for Runt Related Transcription Factor 2 (RUNX2) CLIA Kit Customized Service Offer
n/a ELISA Kit for Runt Related Transcription Factor 2 (RUNX2) ELISA Kit Customized Service Offer
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  3. "The DNA sequence and analysis of human chromosome 6." Nature 425:805-811(2003) [PubMed] [Europe PMC] [Abstract]
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  5. "The cDNA cloning of the transcripts of human PEBP2alphaA/CBFA1 mapped to 6p12.3-p21.1, the locus for cleidocranial dysplasia."Oncogene 15:367-371(1997) [PubMed] [Europe PMC] [Abstract]
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  7. "MOZ and MORF histone acetyltransferases interact with the Runt-domain transcription factor Runx2."Oncogene 21:2729-2740(2002) [PubMed] [Europe PMC] [Abstract]
  8. "Cell cycle-dependent phosphorylation of the RUNX2 transcription factor by cdc2 regulates endothelial cell proliferation."J. Biol. Chem. 281:7118-7128(2006) [PubMed] [Europe PMC] [Abstract]
  9. "Foxp3 controls regulatory T-cell function by interacting with AML1/Runx1."Nature 446:685-689(2007) [PubMed] [Europe PMC] [Abstract]
  10. "Combining protein-based IMAC, peptide-based IMAC, and MudPIT for efficient phosphoproteomic analysis."J. Proteome Res. 7:1346-1351(2008) [PubMed] [Europe PMC] [Abstract]
  11. "Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly is caused by a duplication in RUNX2."Am. J. Hum. Genet. 92:252-258(2013) [PubMed] [Europe PMC] [Abstract]
  12. "Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia."Nat. Genet. 16:307-310(1997) [PubMed] [Europe PMC] [Abstract]
  13. "Mutation analysis of core binding factor A1 in patients with cleidocranial dysplasia."Am. J. Hum. Genet. 65:1268-1278(1999) [PubMed] [Europe PMC] [Abstract]
  14. "CBFA1 mutation analysis and functional correlation with phenotypic variability in cleidocranial dysplasia."Hum. Mol. Genet. 8:2311-2316(1999) [PubMed] [Europe PMC] [Abstract]
  15. "PEBP2alphaA/CBFA1 mutations in Japanese cleidocranial dysplasia patients."Gene 244:21-28(2000) [PubMed] [Europe PMC] [Abstract]
  16. "A novel CBFA1 mutation (R190W) in an Italian family with cleidocranial dysplasia."Hum. Mutat. 16:277-277(2000) [PubMed] [Europe PMC] [Abstract]
  17. "Functional analysis of RUNX2 mutations in Japanese patients with cleidocranial dysplasia demonstrates novel genotype-phenotype correlations."Am. J. Hum. Genet. 71:724-738(2002) [PubMed] [Europe PMC] [Abstract]
  18. "New mutations in the CBFA1 gene in two Mexican patients with cleidocranial dysplasia."Clin. Genet. 61:349-353(2002) [PubMed] [Europe PMC] [Abstract]
  19. "Cleidocranial dysplasia with decreased bone density and biochemical findings of hypophosphatasia."Eur. J. Pediatr. 161:619-622(2002) [PubMed] [Europe PMC] [Abstract]
  20. "Mutations in the RUNX2 gene in patients with cleidocranial dysplasia."Hum. Mutat. 19:209-216(2002) [PubMed] [Europe PMC] [Abstract]
  21. "Four novel RUNX2 mutations including a splice donor site result in the cleidocranial dysplasia phenotype."J. Cell. Physiol. 207:114-122(2006) [PubMed] [Europe PMC] [Abstract]
  22. "A novel RUNX2 mutation (T420I) in Chinese patients with cleidocranial dysplasia."Genet. Mol. Res. 9:41-47(2010) [PubMed] [Europe PMC] [Abstract]
  23. "Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia."Hum. Mutat. 31:E1587-E1593(2010) [PubMed] [Europe PMC] [Abstract]
  24. "RUNX2 mutations in cleidocranial dysplasia patients."Oral Dis. 16:55-60(2010) [PubMed] [Europe PMC] [Abstract]