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FITC标记的血管生成素相关蛋白5
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更新日期：2026/8/7 18:14:45
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相关标签：FITC标记的血管生成素相关蛋白5
详细内容
| 英文名称 | Anti-ANGPTL5/FITC |
| 中文名称 | FITC标记的血管生成素相关蛋白5 |
| 别 名 | Angiopoietin like 5; Angiopoietin related protein 5; Angiopoietin-like protein 5; Angiopoietin-related protein 5; ANGL5_HUMAN; ANGPTL 5; ANGPTL5; Fibrinogen like; hide |
| 说 明 书 | 100ul |
| 研究领域 | 心血管 生长因子和激素 |
| 抗体来源 | Rabbit |
| 克隆类型 | Polyclonal |
| 交叉反应 | Human, Chicken, Pig, Horse, Sheep, |
| 产品应用 | IF=1:50-200 not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
| 分 子 量 | 41kDa |
| 性 状 | Lyophilized or Liquid |
| 浓 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from human ANGPTL5 |
| 亚 型 | IgG |
| 纯化方法 | affinity purified by Protein A |
| 储 存 液 | Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4 |
| 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: Angptl5 (angiopoietin-like 5) is a 388 amino acid secreted protein that contains one fibrinogen C-terminal domain ａnd is primarily expressed in adult heart tissue. The gene encoding Angptl5 maps to human chromosome 11. With approximately 135 million base pairs ａnd 1,400 genes, chromosome 11 comprises approximately 4% of human genomic DNA ａnd is considered a gene ａnd disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest ａnd apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia ａnd thalassemia are caused by HBB gene mutations, while Wilms＇ tumors, WAGR syndrome ａnd Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell ａnd Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema ａnd Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11-encoded genes. Subcellular Location: Secreted (Potential). Tissue Specificity: Mainly expressed in adult heart. Similarity: Contains 1 fibrinogen C-terminal domain. Database links: Entrez Gene: 253935 Human Omim: 607666 Human SwissProt: Q86XS5 Human Unigene: 318370 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
FITC标记的血管生成素相关蛋白5
