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Validated All-in-One™ qPCR Primer for MAFB(NM_005461.4) Search again
By default, qPCR primer pairs are designed to measure the expression level of the splice variant (accession number) you selected for this gene WITHOUT consideration of other possible variants of this gene. If this gene has multiple variants, and you would like to measure the expression levels of one particular variant, multiple variants, or all variants, please contact us for a custom service project at inquiry@genecopoeia.com.
Validated result:
Summary
The protein encoded by this gene is a basic leucine zipper (bZIP) transcription factor that plays an important role in the regulation of lineage-specific hematopoiesis. The encoded nuclear protein represses ETS1-mediated transcription of erythroid-specific genes in myeloid cells. This gene contains no introns. [provided by RefSeq].
Gene References into function
- strong proliferative signals mediated by T-cell activation and interleukins (IL-4 and IL-12) downregulate the mafB messenger RNA transcript level when resting naive CD4+ T-helper cells enter the differentiation pathway in vitro.
- Our data show that human monocytes, but not neutrophils, macrophages, dendritic or natural killer cells, downregulate the expression of Mac-1 after overnight exposure to surface-bound IgG.
- novel role for MafB as a regulator of ERK-induced gene expression
- Low-density lipoprotein receptor-related protein intracellular domain co-localizes with MafB to the nucleus and negatively regulates its transcriptional activity
- high PU.1 activity favors dendritic cells at the expense of macrophage fate by inhibiting expression and activity of the macrophage factor MafB.
- MafB is a key regulator of monocytopoiesis
- Microarray analysis of Dupuytren's disease tissue has identified significant upregulated gene expression of MafB
- Large Maf proteins (MafA, MafB and c-Maf) are implicated in human cancers.
- the vitamin D(3)/Hox-A10 pathway supports MafB function during the induction of monocyte differentiation.
- Identification of primary MAFB target genes in multiple myeloma
