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TBLR1 mouse mAb

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货号: PH1282
货期: 一周
价格: 100μL/2200
+

所属分类:


靶点: TBLR1
应用: WB,IHC,ICC
反应性 : Human,Mouse
宿主物种 : Mouse
MW(Observed): 60kD

隐藏域元素占位

详细信息

推荐稀释比 : WB 1:1000;ICC 1:200 1:500-1:1000
组成 : Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
纯化工艺 : The antibody was affinity-purified from mouse ascites by affinity-chromatography using epitope-specific immunogen.
储存 : -15°C to -25°C/1 year(Do not lower than -25°C
克隆性 : Monoclonal

抗原&靶点信息

特异性 : This antibody detects endogenous levels of TBLR1 and does not cross-react with related proteins.
基因名称 : tbl1xr1
蛋白名称 : F-box-like/WD repeat-containing protein TBL1XR1
别名 : TBL1XR1;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;Transducin;beta;like 1 X linked receptor 1;Transducin beta like 1X related protein 1;Transducin beta-like 1X-related protein 1.

数据库链接:

Organism

基因 ID

SwissProt

Mouse
背景:

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],

细胞定位 : Nucleus .

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