FBX32 rabbit pAb

FBX32 rabbit pAb

AO-06-ES16504-50

FBX32 rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES16504
Product nameFBX32 rabbit pAb
ReactivityHuman; Mouse;Rat
ApplicationsWB
Other nameF-box only protein 32 (Atrogin-1) (Muscle atrophy F-box protein) (MAFbx)
Size50μL
Unit price ($)148
Human gene ID114907
Human Swiss-ProtQ969P5
SourceRabbit
IsotypeIgG
TargetFBX32
Fields>>FoxO signaling pathway
Gene nameFBXO32
Protein nameFBX32
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID67731
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ9CPU7
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID171043
Rat gene linkView Rat Gene
Rat Swiss-ProtQ91Z62
Rat Swiss linkView Rat Swiss-Prot
ImmunogenSynthesized peptide derived from human FBX32 AA range: 217-267
SpecificityThis antibody detects endogenous levels of FBX32 at Human/Mouse/Rat
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.66% sodium azide.
ClonalityPolyclonal
DilutionWB 1:500-2000
PurificationThe antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)38kD
BackgroundThis gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class and contains an F-box domain. This protein is highly expressed during muscle atrophy, whereas mice deficient in this gene were found to be resistant to atrophy. This protein is thus a potential drug target for the treatment of muscle atrophy. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2011],
Functionfunction:Substrate recognition component of a (SKP1-CUL1-F-box protein) E3 ubiquitin-protein ligase complex which mediates the ubiquitination and subsequent proteasomal degradation of target proteins. Probably recognizes and binds to phosphorylated target proteins during skeletal muscle atrophy. Recognizes TERF1.,pathway:Protein modification; protein ubiquitination.,similarity:Contains 1 F-box domain.,subunit:Part of the SCF (SKP1-CUL1-F-box) E3 ubiquitin-protein ligase complex SCF(FBXO32) formed of CUL1, SKP1A, RBX1 and FBXO32.,tissue specificity:Specifically expressed in cardiac and skeletal muscle.,
Subcellular locationCytoplasm . Nucleus . Shuttles between cytoplasm and the nucleus.
ExpressionSpecifically expressed in cardiac and skeletal muscle.

Additional Images

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Western blot analysis of lysates from HpeG2 cells, primary antibody was diluted at 1:1000, 4°over night
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: AO-06-ES16504-50
: 10 Items
Hurry! only 10 items left in stock.

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