anti-GTF2IRD1 antibody
CAT.NO. : ARG41180
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概述
产品描述 | Rabbit Polyclonal antibody recognizes GTF2IRD1 |
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反应物种 | Hu, Ms, Rat |
应用 | WB |
宿主 | Rabbit |
克隆 | Polyclonal |
同位型 | IgG |
靶点名称 | GTF2IRD1 |
抗原物种 | Human |
抗原 | Recombinant fusion protein corresponding to aa. 660-959 of Human GTF2IRD1 (NP_057412.1). |
偶联标记 | Un-conjugated |
別名 | WBSCR11; RBAP2; WBSCR12; BEN; WBS; Williams-Beuren syndrome chromosomal region 11 protein; Williams-Beuren syndrome chromosomal region 12 protein; GTF2I repeat domain-containing protein 1; Slow-muscle-fiber enhancer-binding protein; MUSTRD1; USE B1-binding protein; General transcription factor II-I repeat domain-containing protein 1; GTF3; CREAM1; MusTRD1/BEN; hMusTRD1alpha1; General transcription factor III; Muscle TFII-I repeat domain-containing protein 1 |
应用说明
应用建议 |
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应用说明 | * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist. | ||||
阳性对照 | BT-474 | ||||
实际分子量 | 110 kDa |
属性
形式 | Liquid |
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纯化 | Affinity purified. |
缓冲液 | PBS (pH 7.3), 0.02% Sodium azide and 50% Glycerol. |
抗菌剂 | 0.02% Sodium azide |
稳定剂 | 50% Glycerol |
存放说明 | For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use. |
注意事项 | For laboratory research only, not for drug, diagnostic or other use. |
生物信息
数据库连接 | Swiss-port # Q9JI57 Mouse General transcription factor II-I repeat domain-containing protein 1 Swiss-port # Q9UHL9 Human General transcription factor II-I repeat domain-containing protein 1 |
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基因名称 | GTF2IRD1 |
全名 | GTF2I repeat domain containing 1 |
背景介绍 | The protein encoded by this gene contains five GTF2I-like repeats and each repeat possesses a potential helix-loop-helix (HLH) motif. It may have the ability to interact with other HLH-proteins and function as a transcription factor or as a positive transcriptional regulator under the control of Retinoblastoma protein. This gene plays a role in craniofacial and cognitive development and mutations have been associated with Williams-Beuren syndrome, a multisystem developmental disorder caused by deletion of multiple genes at 7q11.23. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2010] |
生物功能 | May be a transcription regulator involved in cell-cycle progression and skeletal muscle differentiation. May repress GTF2I transcriptional functions, by preventing its nuclear residency, or by inhibiting its transcriptional activation. May contribute to slow-twitch fiber type specificity during myogenesis and in regenerating muscles. Binds troponin I slow-muscle fiber enhancer (USE B1). Binds specifically and with high affinity to the EFG sequences derived from the early enhancer of HOXC8 (By similarity). [UniProt] |
细胞定位 | Nucleus. [UniProt] |
预测分子量 | 106 kDa |
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