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Catalog: YM1250
Size
Price
Status
Qty.
200μL
$450.00
3 weeks

0

100μL
$280.00
3 weeks

0

40μL
$160.00
3 weeks

0

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Main Information
Target

TBLR1

Host Species

Mouse

Reactivity

Human, Mouse

Applications

WB, IHC, ICC

MW

60kD (Observed)

Conjugate/Modification


Unmodified

Detailed Information
Recommended Dilution Ratio
WB 1:1000; ICC 1:200 1:500-1:1000
Formulation
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Specificity
This antibody detects endogenous levels of TBLR1 and does not cross-react with related proteins.
Purification
The antibody was affinity-purified from mouse ascites by affinity-chromatography using epitope-specific immunogen.
Storage
-15°C to -25°C/1 year(Do not lower than -25°C)
MW(Observed)
60kD
Modification
Unmodified
Clonality
Monoclonal
Clone Number
1F8
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Antigen&Target Information
Immunogen:
Purified recombinant human TBLR1 protein fragments expressed in E.coli.
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Specificity:
This antibody detects endogenous levels of TBLR1 and does not cross-react with related proteins.
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Gene Name:
tbl1xr1
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Other Name:
C21 ;
DC42 ;
F box like/WD repeat containing protein TBL1XR1 ;
F-box-like/WD repeat-containing protein TBL1XR1 ;
FLJ12894 ;
IRA1 ;
Nuclear receptor corepressor/HDAC3 complex subunit ;
Nuclear receptor corepressor/HDAC3 complex subunit TBLR1 ;
TBL1 related protein 1 ;
TBL1-related protein 1 ;
TBL1R_HUMAN ;
TBL1XR1 ;
Transducin ;
beta ;
like 1 X linked receptor 1 ;
Transducin beta like 1X related protein 1 ;
Transducin beta-like 1X-related protein 1.
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Database Link:
Organism Gene ID SwissProt
Human 79718; Q9BZK7;
Mouse Q8BHJ5;
Background:
This gene is a member of the WD40 repeat-containing gene family and shares sequence similarity with transducin (beta)-like 1X-linked (TBL1X). The protein encoded by this gene is thought to be a component of both nuclear receptor corepressor (N-CoR) and histone deacetylase 3 (HDAC 3) complexes, and is required for transcriptional activation by a variety of transcription factors. Mutations in these gene have been associated with some autism spectrum disorders, and one finding suggests that haploinsufficiency of this gene may be a cause of intellectual disability with dysmorphism. Mutations in this gene as well as recurrent translocations involving this gene have also been observed in some tumors. [provided by RefSeq, Mar 2016],
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Function:
Domain:The F-box-like domain is related to the F-box domain, and apparently displays the same function as component of ubiquitin E3 ligase complexes.,Function:F-box-like protein involved in the recruitment of the ubiquitin/19S proteasome complex to nuclear receptor-regulated transcription units. Plays an essential role in transcription activation mediated by nuclear receptors. Probably acts as integral component of the N-Cor corepressor complex that mediates the recruitment of the 19S proteasome complex, leading to the subsequent proteosomal degradation of N-Cor complex, thereby allowing cofactor exchange, and transcription activation.,PTM:Phosphorylated upon DNA damage, probably by ATM or ATR.,sequence Caution:Contaminating sequence. Potential poly-A sequence.,similarity:Belongs to the WD repeat EBI family.,similarity:Contains 1 F-box-like domain.,similarity:Contains 1 LisH domain.,similarity:Contains 8 WD repeats.,subunit:Component of the N-Cor repressor complex, at least composed of NCOR1, NCOR2, HDAC3, TBL1X, TBL1XR1, CORO2A and GPS2. Probable component of some E3 ubiquitin ligase complex. Interacts with histones H2B and H4.,tissue specificity:Ubiquitous.,
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Cellular Localization:
Nucleus .
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Research Areas:
>>Wnt signaling pathway
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Catalog: YM1250
Size
Price
Status
Qty.
200μL
$450.00
3 weeks

0

100μL
$280.00
3 weeks

0

40μL
$160.00
3 weeks

0

Add to cart

Collected

Collect

Customized Service

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