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Rabbit Anti-FOXD1/FITC Conjugated antibody
background:
FOXD1 is involved in regulating inflammation as well as kidney and retinal development. FOXD1 regulates the activity of NFAT and NFkB. Deficiency of FOXD1 results in multiorgan systemic inflammation, exaggerated Th cell-derived cytokine production, and T cell proliferation in autogolgous MLRs. In kidneys, FOXD1 controls the production of signals required for the normal transition of induced mesenchyme into tubular epithelium and full growth and branching of the collecting system. Deletion of FOXD1 results in renal abnormalities. FOXD2 acts as a modulator of T cell activation.
Function:
Transcription factor required for formation of positional identity in the developing retina, regionalization of the optic chiasm and morphogenesis of the kidney. Can neuralize ectodermal cells directly.
Subcellular Location:
Nucleus.
Similarity:
Contains 1 fork-head DNA-binding domain.
Database links:
Entrez Gene: 2297 Human
Entrez Gene: 15229 Mouse
GenBank: NP_004463 Human
Omim: 601091 Human
SwissProt: Q16676 Human
SwissProt: Q61345 Mouse
Unigene: 519385 Human
Unigene: 347441 Mouse
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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