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TBP/TATA Binding Protein Monoclonal Antibody(1F6)

货号：YM3515
应用：IHC;IF
种属：Human;Rat;Mouse

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靶点：
TBP/TATA Binding Protein

简介：
>>Basal transcription factors;>>Huntington disease;>>Spinocerebellar ataxia;>>Human papillomavirus infection;>>Human T-cell leukemia virus 1 infection;>>Viral carcinogenesis

基因名称：
TBP

蛋白名称：
TATA-box-binding protein (TATA sequence-binding protein) (TATA-binding factor) (TATA-box factor) (Transcription initiation factor TFIID TBP subunit)

Human Gene Id：
6908

Human Swiss Prot No：
P20226

Mouse Swiss Prot No：
P29037

免疫原：
Recombinant Protein of TBP/TATA Binding Protein

特异性：
TBP/TATA Binding Protein protein detects endogenous levels of TBP/TATA Binding Protein

组成：
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

来源：
Monoclonal, Mouse

稀释：
IHC 1:50-200. IF 1:50-200

纯化工艺：
The antibody was affinity-purified from mouse ascites by affinity-chromatography using specific immunogen.

浓度：
1 mg/ml

储存：
-15°C to -25°C/1 year(Do not lower than -25°C)

其他名称：
TBP;GTF2D1;TF2D;TFIID;TATA-box-binding protein;TATA sequence-binding protein;TATA-binding factor;TATA-box factor;Transcription initiation factor TFIID TBP subunit

实测条带：
35-45kD

背景：
Initiation of transcription by RNA polymerase II requires the activities of more than 70 polypeptides. The protein that coordinates these activities is transcription factor IID (TFIID), which binds to the core promoter to position the polymerase properly, serves as the scaffold for assembly of the remainder of the transcription complex, and acts as a channel for regulatory signals. TFIID is composed of the TATA-binding protein (TBP) and a group of evolutionarily conserved proteins known as TBP-associated factors or TAFs. TAFs may participate in basal transcription, serve as coactivators, function in promoter recognition or modify general transcription factors (GTFs) to facilitate complex assembly and transcription initiation. This gene encodes TBP, the TATA-binding protein. A distinctive feature of TBP is a long string of glutamines in the N-terminus. This region of the protein modulates the DNA bin

功能：
disease:Defects in TBP are the cause of spinocerebellar ataxia type 17 (SCA17) [MIM:607136]. Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCA17 is an autosomal dominant cerebellar ataxia (ADCA) characterized by widespread cerebral and cerebellar atrophy, dementia and extrapyramidal signs. The molecular defect in SCA17 is the expansion of a CAG repeat in the coding region of TBP. Longer expansions result in earlier onset and more severe clinical manifestations of the disease.,function:General transcription factor that functions at the core of the DNA-binding multiprotein factor TFIID. Binding of TFIID to the TATA box is the ini

细胞定位：
Nucleus .

组织表达：
Widely expressed, with levels highest in the testis and ovary.

Jiang, Qianqian, et al. "BMP9 promotes methionine-and choline-deficient diet-induced nonalcoholic steatohepatitis in non-obese mice by enhancing NF-κB dependent macrophage polarization." International Immunopharmacology 96 (2021): 107591.
货号：YM3515