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>   Home   >   Products   >   Primary Antibodies   >   [KO] FBXO11 Mouse mAb   

[KO] FBXO11 Mouse mAb

 
Catalog #
ABZ1196
Application
WB
Uniprot Id
Q86XK2
Reactivity
Rat
Isotype
IgG1
 
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 Catalog #AvailabilitySizeQuantityUnit Price Save For Later Wish List
ABZ1196-100 2 weeks 100 µL $499.00
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ABZ1196-20 2 weeks 20 µL $149.00
ABZ1196-50 2 weeks 50 µL $325.00
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Product Overview

Name[KO] FBXO11 Mouse mAb
Accession (Primary)Q86XK2
Host SpeciesMouse
IsotypeIgG1
Immunogen
Purified recombinant human FBXO11 protein fragments expressed in E.coli.
Species Reactivity
Reacts WithRat
Calculated MW
Calculated MW: 104 kDa; Observed MW: 104 kDa
Buffer System
Liquid in PBS containing 50% glycerol, 1% BSA and 0.02% sodium azide, pH 7.3.
Storage
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Recommended Dilution
WB: 1/500-1/1000
Clonality No.
1E3
Purification
Affinity Purified
Conjugation
Unconjugated
Modification
Unmodified
Form
Liquid
Background
This 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 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. It can function as an arginine methyltransferase that symmetrically dimethylates arginine residues, and it acts as an adaptor protein to mediate the neddylation of p53, which leads to the suppression of p53 function. This gene is known to be down-regulated in melanocytes from patients with vitiligo, a skin disorder that results in depigmentation. Polymorphisms in this gene are associated with chronic otitis media with effusion and recurrent otitis media (COME/ROM), a hearing loss disorder, and the knockout of the homologous mouse gene results in the deaf mouse mutant Jeff (Jf), a single gene model of otitis media. Alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jun 2010]
Research Field
Cell Biology

Target Information: ( Q86XK2 )

NameFBXO11
Other Names
FBX11; PRMT9; UBR6; UG063H01; VIT1
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