FITC标记的叉头蛋白D1抗体
产品名称： FITC标记的叉头蛋白D1抗体
英文名称： Anti-FOXD1/FITC
产品编号： HZ-12193R-FITC
产品价格： null
产品产地： 中国/上海
品牌商标： HZbscience
更新时间： 2023-08-17T10:24:20
使用范围： ICC=1:50-200 IF=1:50-200
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Rabbit Anti-FOXD1/FITC Conjugated antibody
FITC标记的叉头蛋白D1抗体
| 英文名称 | Anti-FOXD1/FITC |
| 中文名称 | FITC标记的叉头蛋白D1抗体 |
| 别 名 | Brain Factor 2; FKH L8; FKHL 8; FKHL8; Forkhead (Drosophila) like 8; Forkhead box D1; Forkhead box protein D1; Forkhead drosophila homolog like 8; Forkhead like 8; Forkhead related activator 4; Forkhead related protein FKHL8; Forkhead related transcription factor 4; Forkhead-related protein FKHL8; Forkhead-related transcription factor 4; FOX D1; FOXD 1; foxd1; FOXD1_HUMAN; FREAC 4; FREAC-4; FREAC4. |
| 规格价格 | 100ul/2980元 购买 大包装/询价 |
| 说 明 书 | 100ul |
| 研究领域 | 细胞生物 发育生物学 神经生物学 干细胞 转录调节因子 细胞分化 |
| 抗体来源 | Rabbit |
| 克隆类型 | Polyclonal |
| 交叉反应 | Human, Mouse, Chicken, Dog, Rabbit, Sheep, |
| 产品应用 | ICC=1:50-200 IF=1:50-200 not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
| 分 子 量 | 46kDa |
| 性 状 | Lyophilized or Liquid |
| 浓 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from Human FOXD1 |
| 亚 型 | IgG |
| 纯化方法 | affinity purified by Protein A |
| 储 存 液 | 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. |
| 保存条件 | Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C. |
| 产品介绍 | background: FOXD1 is involved in regulating inflammation as well as kidney and retinal development. FOXD1 regulates the activity of NFAT and NFkB. Deficiency of FOXD1 results in multiorgan systemic inflammation, exaggerated Th cell-derived cytokine production, and T cell proliferation in autogolgous MLRs. In kidneys, FOXD1 controls the production of signals required for the normal transition of induced mesenchyme into tubular epithelium and full growth and branching of the collecting system. Deletion of FOXD1 results in renal abnormalities. FOXD2 acts as a modulator of T cell activation. Function: Transcription factor required for formation of positional identity in the developing retina, regionalization of the optic chiasm and morphogenesis of the kidney. Can neuralize ectodermal cells directly. Subcellular Location: Nucleus. Similarity: Contains 1 fork-head DNA-binding domain. Database links: Entrez Gene: 2297 Human Entrez Gene: 15229 Mouse GenBank: NP_004463 Human Omim: 601091 Human SwissProt: Q16676 Human SwissProt: Q61345 Mouse Unigene: 519385 Human Unigene: 347441 Mouse Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications |
FXD1参与调节炎症以及肾脏和视网膜发育。FXD1调节NFAT和NFKB的活性。FOXD1缺乏导致自体MLR多器官全身炎症、Th细胞衍生细胞因子过度生成和T细胞增殖。在肾脏中，FOXD1控制所诱导的间充质向肾小管上皮的正常转变以及收集系统的完全生长和分支所需的信号的产生。FXD1的缺失导致肾脏异常。FXD2作为T细胞活化的调节剂。