RUNX2 Polyclonal Antibody


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Cat.No.:  EAb-0313
Product Name:  RUNX2 Polyclonal Antibody
Antibody Type:  Polyclonal
Immunogen:  Recombinant protein of human RUNX2
Host:  Rabbit
Isotype:  IgG
Purification:  Affinity purification
Appearance:  Liquid
Applications:  WB
Recommended Dilutions/Conditions:  WB: 1:200 - 1:1000
Recommended dilutions/conditions may not be available for all applications. Specific conditions for reactivity should be optimized by the end user.
Species Reactivity:  Human, Mouse
Storage:  -20°C
Storage Buffer:  PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Warning:  For Research Use Only! Not For Use in Humans.
Accession:  Q13950
Alternative Name:  Acute myeloid leukemia 3 protein,Alpha subunit 1,AML3,CBF alpha 1,CBF-alpha-1,CBFA1,CCD,CCD1,Cleidocranial dysplasia 1,Core binding factor,Core binding factor runt domain alpha subunit 1,Core binding factor subunit alpha 1,Core-binding factor subunit alpha-1,MGC120022,MGC120023,Oncogene AML 3,Oncogene AML-3,OSF 2,OSF-2,OSF2,Osteoblast specific transcription factor 2,Osteoblast-specific transcription factor 2,OTTHUMP00000016533,PEA2 alpha A,PEA2-alpha A,PEA2aA,PEBP2 alpha A,PEBP2-alpha A,PEBP2A1,PEBP2A2,PEBP2aA,PEBP2aA1,Polyomavirus enhancer binding protein 2 alpha A subunit,Polyomavirus enhancer-binding protein 2 alpha A subunit,Runt domain,Runt related transcription factor 2,Runt-related transcription factor 2,RUNX2,RUNX2,SL3 3 enhancer factor 1 alpha A subunit,SL3-3 enhancer factor 1 alpha A subunit,SL3/AKV core binding factor alpha A subunit,SL3/AKV core-binding factor alpha A subunit
Scientific Background:  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. Two regions of potential trinucleotide repeat expansions are present in the N-terminal region of the encoded protein, and these and other 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.
Product Types
◆ Antibodies
EAb-0042 Runx1/AML1-ETO Polyclonal Antibody Inquiry
EAb-0313 RUNX2 Polyclonal Antibody Inquiry
◆ Extracts & Lysates
EL-0092 Recombinant Human RUNX2 293 Cell Lysate Inquiry
EL-0093 Recombinant Human RUNX2 293 Cell Lysate Inquiry
◆ Proteins & Enzymes
PE-0746 Recombinant Human RUNX2 Inquiry
Related Gene / Proteins
Runx1 RUNX2 RUVB2 RUVBL1

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For Research Use Only. Not for use in diagnostic or therapeutic procedures.

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