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转录因子Tbx18抗体

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产品名称: 转录因子Tbx18抗体
产品型号: TBX18
产品展商: 单克隆抗体/多克隆抗体
产品文档: 无相关文档

简单介绍

转录因子Tbx18抗体应用于IHC、WB、 IF、IP、ELISA等科研实验,按理化性质和生物学功能IgM、IgG、IgA、IgE、IgD五类。按抗体的来源,可将其分为天然抗体和**抗体。转录因子Tbx18抗体生产每个流程都执行严格的检测标准,保证蛋白抗原产品质量,质量稳定,实验效果明显。


转录因子Tbx18抗体  的详细介绍

转录因子Tbx18抗体

规格:1mg/1ml

英文名: TBX18

别名: T box 18; T box protein 18; T box transcription factor TBX18; T-box protein 18; T-box transcription factor TBX18; TBX18; TBX18_HUMAN.

分子量: 65kDa

储存液:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce

克隆类型:Polyclonal

亚型:IgG

纯化方法:affinity purified by Protein A

**原:KLH conjugated synthetic peptide derived from human TBX18

交叉反应:Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit,

细胞定位:细胞核

转录因子Tbx18抗体产品介绍:background: T-box transcription factors are a group of phylogenetically conserved genes that contain a uniquely defining DNA-binding domain, the T-box domain. These genes are believed to be involved in the regulation of development processes, for example the development of limbs, and it is known that haploinsufficiency of multiple T-box proteins results in severe human congenital malformation syndromes, involving craniofacial, cardiovascular, and skeletal structures. TBX 18 has been reported to be involved in numerous development processes and to act as an antiapoptotic factor. Function: Probable transcriptional regulator involved in developmental processes. Subunit: Homodimer. Can form a heterodimer with TBX15. Interacts with GATA4 AND NKX2-5. Interacts with PAX3 (By similarity). 转录因子Tbx18抗体Interacts (via engrailed homology 1 repressor motif) with TLE3; this interaction represses TBX18 transcriptional activity (By similarity) (PubMed:26235987). Interacts with SIX1 (PubMed:26235987). Subcellular Location: Nucleus. DISEASE: Congenital anomalies of kidney and urinary tract 2 (CAKUT2). The disease is caused by mutations affecting the gene represented in this entry. A disorder encompassing a broad spectrum of renal and urinary tract malformations that include renal agenesis, kidney hypodysplasia, multicystic kidney dysplasia, duplex collecting system, 转录因子Tbx18抗体posterior urethral valves and ureter abnormalities. Congenital anomalies of kidney and urinary tract are the commonest cause of chronic kidney disease in children. Similarity: Contains 1 T-box DNA-binding domain. Gene ID: 9096 Database links: Entrez Gene: 9096 Human Entrez Gene: 76365 Mouse Entrez Gene: 315870 Rat Omim: 604613 Human SwissProt: O95935 Human SwissProt: Q9EPZ6 Mouse Unigene: 251830 Human Unigene: 158789 Mouse Unigene: 161921 Rat Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

转录因子Tbx18抗体产品应用:WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 (石蜡切片需做抗原修复) not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.

研究领域:细胞生物  **学  染色质和核信号  转录调节因子  表观遗传学  

储存条件: Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

来源: Rabbit

外观: Lyophilized or Liquid


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