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  • TFII-I (phospho Tyr248) Rabbit Polyclonal Antibody | 兔多抗 | EnkiLife恩玑生命
  • TFII-I (phospho Tyr248) Rabbit Polyclonal Antibody | 兔多抗 | EnkiLife恩玑生命

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TFII-I (phospho Tyr248) Rabbit Polyclonal Antibody | 兔多抗 | EnkiLife恩玑生命

TFII-I (phospho Tyr248) Rabbit Polyclonal Antibody
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湖北 更新日期:2026-01-30

武汉恩玑生命科技有限公司

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联系人:Kiki
电话:027-87002838拨打
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邮箱:order@enkilife.cn

产品详情:

中文名称:
TFII-I (phospho Tyr248)兔多抗
英文名称:
TFII-I (phospho Tyr248) Rabbit Polyclonal Antibody
品牌:
EnkiLife
产地:
中国
产品类别:
抗体
是否进口:
用途:
科研

产品概述

产品名称(Product Name)

TFII-I (phospho Tyr248) Rabbit Polyclonal Antibody

描述(Description)

Rabbit Polyclonal Antibody

宿主(Host)

Rabbit

应用(Application)

WB,ELISA

种属反应性(Reactivity)

Human,Mouse,Rat

 

产品性能

偶联物(Conjugation)

Unconjugated

修饰(Modification)

Phospho Antibody

同种型(Isotype)

IgG

克隆(Clonality)

Polyclonal

形式(Form)

Liquid

存放说明(Storage)

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

储存溶液(Buffer)

Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.

纯化方式(Purification)

Affinity purification

 

免疫原

基因名(Gene Name)

GTF2I

别名(Alternative Names)

GTF2I; BAP135; WBSCR6; General transcription factor II-I; GTFII-I; TFII-I; Bruton tyrosine kinase-associated protein 135; BAP-135; BTK-associated protein 135; SRF-Phox1-interacting protein; SPIN; Williams-Beuren syndrome chromosomal region

基因ID(Gene ID)

2969

蛋白ID(SwissProt ID)

P78347

 

产品应用

稀释比(Dilution Ratio)

WB 1:500-1:2000, ELISA 1:5000.Not yet tested in other applications.

蛋白分子量(Molecular Weight)

115kDa

 

研究背景

general transcription factor IIi(GTF2I) Homo sapiens This gene encodes a phosphoprotein containing six characteristic repeat motifs. The encoded protein binds to the initiator element (Inr) and E-box element in promoters and functions as a regulator of transcription. This locus, along with several other neighboring genes, is deleted in Williams-Beuren syndrome. There are many closely related genes and pseudogenes for this gene on chromosome 7. This gene also has pseudogenes on chromosomes 9, 13, and 21. Alternatively spliced transcript variants encoding multiple isoforms have been observed. [provided by RefSeq, Jul 2013],disease:Haploinsufficiency of GTF2I may be the cause of certain cardiovascular and musculo-skeletal abnormalities observed in Williams-Beuren syndrome (WBS), a rare developmental disorder. It is a contiguous gene deletion syndrome involving genes from chromosome band 7q11.23.,function:Interacts with the basal transcription machinery by coordinating the formation of a multiprotein complex at the C-FOS promoter, and linking specific signal responsive activator complexes. Promotes the formation of stable high-order complexes of SRF and PHOX1 and interacts cooperatively with PHOX1 to promote serum-inducible transcription of a reporter gene deriven by the C-FOS serum response element (SRE). Acts as a coregulator for USF1 by binding independently two promoter elements, a pyrimidine-rich initiator (Inr) and an upstream E-box. Required for the formation of functional ARID3A DNA-binding complexes and for activation of immunoglobulin heavy-chain transcription upon B-lymphocyte activation.,PTM:Sumoylated.,PTM:Transiently phosphorylated on tyrosine residues by BTK in response to B-cell receptor stimulation. Phosphorylation on Tyr-248 and Tyr-398, and perhaps, on Tyr-503 contributes to BTK-mediated transcriptional activation.,similarity:Belongs to the TFII-I family.,similarity:Contains 6 GTF2I-like repeats.,subcellular location:Colocalizes with BTK in the cytoplasm.,subunit:Homodimer (Potential). Interacts with SRF and PHOX1. Binds a pyrimidine-rich initiator (Inr) and a recognition site (E-box) for upstream stimulatory factor 1 (USF1). Associates with the PH domain of Bruton's tyrosine kinase (BTK). May be a component of a BHC histone deacetylase complex that contains HDAC1, HDAC2, HMG20B/BRAF35, AOF2/LSD1, RCOR1/CoREST, PHF21A/BHC80, ZMYM2, ZNF217, ZMYM3, GSE1 and GTF2I. Interacts with BTK and ARID3A.,tissue specificity:Ubiquitous. Isoform 1 is strongly expressed in fetal brain, weakly in adult brain, muscle, and lymphoblasts and is almost undetectable in other adult tissues, while the other isoforms are equally expressed in all adult tissues.,

 

研究领域

Basal transcription factors;

GTF2I;TFII-I;(phospho;Tyr248);Rabbit;Polyclonal;Antibody;一抗

公司简介

武汉恩玑生命科技有限公司(EnkiLife)是一家深耕生命科学,专注细胞生物学和免疫学科研试剂的研发、生产与销售的生物技术企业,在全球100多个国家和地区开展业务,致力于为科研工作者提供高质量的产品和卓越的客户服务,推动生命科学的发展。 EnkiLife的产品线涵盖细胞系、原代细胞、细胞培养基、血清、细胞检测试剂盒、重组靶点蛋白、细胞因子、重组抗体、ELISA试剂盒、生化试剂盒等,并提供技术服务与定制开发,覆盖了生命科学研究的各大关键领域,包括细胞生物学、癌症、免疫学、神经科学、心血管疾病、干细胞、表观遗传学、内分泌、蛋白质组学、代谢组学等,全方位满足您的实验需求,让您享受科研的乐趣! 公司现已建立四大技术平台: EnCyto?细胞培养及检测平台:拥有细胞系库(500+)、原代细胞库(500+)、基础培养基和完全培养基(1200+) EnkiPro?重组蛋白平台:现货产品2000+,可提供定制化表达服务 EnAb?重组抗体平台:重组兔单抗(3000+),可提供定制化和标记服务 EnKits?试剂盒开发平台:可提供优质的ELISA试剂盒、配套试剂、抗体对、生化试剂盒等相关产品 EnkiLife在生产管理方面引入ISO9001质量管理体系和信息化、自动化的管理工具,拥有高效稳定的交付能力,与全球知名品牌建立了紧密的合作。 EnkiLife始终坚持以技术创新为驱动,以匠心铸就品质,以品质服务客户。 我们期待与更多的全球科研工作者和企业携手合作,共同推动生命科学领域的进步与发展。

成立日期 (2年)
注册资本 271万人民币
员工人数 10-50人
年营业额 ¥ 100万-300万
经营模式 工厂,试剂,定制,服务
主营行业 生化试剂,抗体,细胞培养,癌症研究,细胞生物学

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