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MEOX2
This gene encodes a member of a subfamily of non-clustered, diverged, antennapedia-like homeobox-containing genes. The encoded protein may play a role in the regulation of vertebrate limb myogenesis. Mutations in the related mouse protein may be associated with craniofacial and/or skeletal abnormalities, in addition to neurovascular dysfunction observed in Alzheimer's disease.
Protein class
Transcription factors
Predicted location
Intracellular
Single cell type specificity
Cell type enhanced (Adipocytes, Leydig cells, Endothelial cells, Smooth muscle cells, Sertoli cells, Peritubular cells)
Immune cell specificity
Not detected in immune cells
Cell line specificity
Group enriched (AN3-CA, U-138 MG)
Interaction
Interacts with RNF10 (PubMed:16335786). Interacts with TCF15 (By similarity).
Molecular function
Activator, Developmental protein, DNA-binding
More Types Infomation
- Recombinant Mouse Anti-Human MEOX2 Antibody (MOB-1465MZ)
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- Species Reactivity: Human
- Type: Mouse antibody
- Application: WB
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- Derivation: Phage display library screening
- Species Reactivity: Human
- Type: IgG
- Application: WB, IP, FC
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For Research Use Only. Not For Clinical Use.