Lunatic Fringe rabbit pAb

Lunatic Fringe rabbit pAb

AO-06-ES6103-50

Lunatic Fringe rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES6103
Product nameLunatic Fringe rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;ELISA
Other nameLFNG; Beta-1; 3-N-acetylglucosaminyltransferase lunatic fringe; O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
Size50μL
Unit price ($)148
Human gene ID3955
Human Swiss-ProtQ8NES3
SourceRabbit
IsotypeIgG
TargetLunatic Fringe
Fields>>Other types of O-glycan biosynthesis;>>Notch signaling pathway;>>Human papillomavirus infection
Gene nameLFNG
Protein nameBeta-1,3-N-acetylglucosaminyltransferase lunatic fringe
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID16848
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtO09010
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID170905
Rat gene linkView Rat Gene
Rat Swiss-ProtQ924T4
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from human LFNG. AA range:121-170
SpecificityLunatic Fringe Polyclonal Antibody detects endogenous levels of Lunatic Fringe protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. ELISA: 1/10000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)42kD
BackgroundThis gene is a member of the fringe gene family which also includes radical and manic fringe genes. They all encode evolutionarily conserved glycosyltransferases that act in the Notch signaling pathway to define 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. This gene product is predicted to be a single-pass type II Golgi membrane protein but it may also be secreted and proteolytically processed like the related proteins in mouse and Drosophila (PMID: 9187150). Mutations in this gene have been associated with autosomal recessive spondylocostal dysostosis 3. Multiple transcript variants encoding different isoforms
Functionalternative products:Experimental confirmation may be lacking for some isoforms,catalytic activity:Transfers a beta-D-GlcNAc residue from UDP-D-GlcNAc to the fucose residue of a fucosylated protein acceptor.,caution:The sequence shown here is derived from an Ensembl automatic analysis pipeline and should be considered as preliminary data.,disease:Defects in LFNG are the cause of spondylocostal dysostosis autosomal recessive type 3 (SCDO3) [MIM:609813]. Autosomal recessive spondylocostal dysostosis is a rare condition of variable severity associated with vertebral and rib segmentation defects. The main skeletal malformations include fusion of vertebrae, hemivertebrae, fusion of certain ribs, and other rib malformations. Deformity of the chest and spine (severe scoliosis, kyphoscoliosis and lordosis) is a natural consequence of the malformation and leads to a dwarf-like appearance. As the
Subcellular locationGolgi apparatus membrane ; Single-pass type II membrane protein .
ExpressionKidney,

Additional Images

Image 1
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Western Blot analysis of 3T3 cells using Lunatic Fringe Polyclonal Antibody diluted at 1:1000
Image 2
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Western blot analysis of lysates from HUVEC and MCF-7 cells, using LFNG Antibody. The lane on the right is blocked with the synthesized peptide.
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: AO-06-ES6103-50
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Hurry! only 10 items left in stock.

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