FITC标记的21号染色体开放阅读框54抗体
产品名称： FITC标记的21号染色体开放阅读框54抗体
英文名称： Anti-C21orf54/FITC
产品编号： HZ-15137R-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-C21orf54/FITC Conjugated antibody
FITC标记的21号染色体开放阅读框54抗体
| 英文名称 | Anti-C21orf54/FITC |
| 中文名称 | FITC标记的21号染色体开放阅读框54抗体 |
| 别 名 | chromosome 21 open reading frame 54; spliced EST AA934973; CU054_HUMAN. |
| 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 免疫学 |
| 抗体来源 | Rabbit |
| 克隆类型 | Polyclonal |
| 交叉反应 | Human, |
| 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 | 12kDa |
| 性 状 | Lyophilized or Liquid |
| 浓 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from human C21orf54 |
| 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: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The LOC728409 gene product has been provisionally designated LOC728409 pending further characterization. Database links: Entrez Gene: 728409 Human SwissProt: A6NM66 Human Unigene: 125234 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic application |
人类染色体中最小的21个构成了人类基因组的1.5%。第21染色体含有近300个基因和4700万个碱基对。唐氏综合征，又称21三体，是最常见的与21号染色体相关的疾病。阿尔茨海默病、Jever和Lange Nielsen综合征和肌萎缩侧索硬化也与第21号染色体有关。在某些白血病中，染色体易位发生在21号染色体和8号染色体之间，以及染色体21和12之间。Lo78409基因产物已暂时指定为ROC728 409，有待进一步鉴定。