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Antibody detects endogenous levels of total Myelodysplasia Syndrome 1.
The MECOM gene (MDS1 and EVI1 Complex Locus) is located on chromosome 3q26.2 and encodes a protein involved in transcriptional regulation. This gene produces multiple transcript variants encoding different isoforms, including MDS1, EVI1, and PRDM3. The EVI1 protein, one of the main isoforms, is characterized by zinc finger motifs, which facilitate DNA binding, and a SET domain responsible for methyltransferase activity. MECOM plays a crucial role in cell proliferation, differentiation, apoptosis, and hematopoiesis. Aberrations in MECOM, particularly overexpression or rearrangements, are associated with various hematological malignancies, including acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS). The MECOM gene's normal function and pathological alterations make it a significant target for research in cancer biology and therapeutics.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: AML1-EVI-1 fusion protein; Ecotropic virus integration site 1 protein homolog; EVI-1; Histone-lysine N-methyltransferase MECOM; MDS1; MDS1 and EVI1 complex locus protein; MDS1 and EVI1 complex locus protein EVI1; MDS1 and EVI1 complex locus protein MDS1; Myelodysplasia syndrome 1 protein; Myelodysplasia syndrome-associated protein 1; oncogene EVI1; PR domain 3; unnamed protein product; zinc finger protein Evi1
Gene Aliases: AML1-EVI-1; EVI1; KMT8E; MDS1; MDS1-EVI1; MECOM; PRDM3; RUSAT2
UniProt ID: (Human) Q03112
Entrez Gene ID: (Human) 2122
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