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anti-Human Manic Fringe Antibodies:
anti-Mouse (Murine) Manic Fringe Antibodies:
anti-Rat (Rattus) Manic Fringe Antibodies:
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Cow (Bovine) Polyclonal Manic Fringe Primary Antibody for IHC (p), ELISA - ABIN2475483
Bray: Notch signalling: a simple pathway becomes complex. in Nature reviews. Molecular cell biology 2006
Mfng is an oncogene (show RAB1A Antibodies) acting through Notch (show NOTCH1 Antibodies)-mediated induction of Pik3cg (show PIK3CG Antibodies).
These results show that Notch (show NOTCH1 Antibodies) signaling is finely calibrated in the cochlea via Lfng (show LFNG Antibodies) and Mfng to produce precisely tuned levels of signaling that first set the boundary of the organ of Corti and later regulate hair cell development.
Fringe modifications at EGF8 and EGF12 enhanced Notch1 binding to and activation from Delta-like 1, while modifications at EGF6 and EGF36 (added by Manic and Lunatic but not Radical) inhibited Notch1 activation from Jagged1.
the presence of Gal (show GAL Antibodies) on O-fucose glycans differentially affects DLL1 (show DLL1 Antibodies)-induced NOTCH (show NOTCH1 Antibodies) signaling modulated by LFNG (show LFNG Antibodies) versus MFNG
Myt1 (show MYT1 Antibodies), Myt3, and Ngn3 (show NEUROG3 Antibodies) are induced by Mfng and have roles in Mfng-mediated repression of Notch (show NOTCH1 Antibodies) signaling which could serve as a trigger for endocrine islet differentiation
Jag1 (show JAG1 Antibodies)/fringe genes (Lfng (show LFNG Antibodies), Rfng, and Mfng) may regulate postnatal bile duct growth and remodeling, and serve as candidate modifiers of the hepatic phenotype in Alagille syndrome.
Lunatic Fringe (Lfng (show LFNG Antibodies)) and Manic Fringe (Mfng) cooperatively enhanced the DL1-Notch2 (show NOTCH2 Antibodies) interaction to promote marginal zone B cell development
MFng colocalized with the proendocrine transcription factor Ngn3 (show NEUROG3 Antibodies) in the developing mouse pancreas between embryonic days 9 and 14
This gene is a member of the fringe gene family which also includes radical and lunatic fringe genes. They all encode evolutionarily conserved secreted proteins that act in the Notch receptor pathway to demarcate boundaries during embryonic development. While their genomic structure is distinct from other glycosyltransferases, fringe proteins have a fucose-specific beta-1,3-N-acetylglucosaminyltransferase activity that leads to elongation of O-linked fucose residues on Notch, which alters Notch signaling.
, beta-1,3-N-acetylglucosaminyltransferase manic fringe
, manic fringe homolog