FITC标记的18号染色体开放阅读框56抗体
产品名称： FITC标记的18号染色体开放阅读框56抗体
英文名称： Anti-C18orf56/FITC
产品编号： HZ-9675R-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
上海沪震实业有限公司
- 联系人 : 鲍丽雯
- 地址 : 上海市闵行区闵北路88弄1-30号第22幢AQ136室
- 邮编 : 200612
- 所在区域 : 上海
- 电话 : 139****0749 点击查看
- 传真 : 点击查看
- 邮箱 : www.shzbio.net
- 二维码 : 点击查看
Rabbit Anti-C18orf56/FITC Conjugated antibody
FITC标记的18号染色体开放阅读框56抗体
| 产品编号 | bs-9675R-FITC |
| 英文名称 | Anti-C18orf56/FITC |
| 中文名称 | FITC标记的18号染色体开放阅读框56抗体 |
| 别 名 | Putative uncharacterized protein C18orf56; CR056_HUMAN. |
| 规格价格 | 100ul/2980元 购买 大包装/询价 |
| 说 明 书 | 100ul |
| 研究领域 | 心血管 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 | 13kDa |
| 性 状 | Lyophilized or Liquid |
| 浓 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from human C18orf56 |
| 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: Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGFβ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18. The C18orf56 gene product has been provisionally designated C18orf56 pending further characterization. Database links: Entrez Gene: 494514 Human SwissProt: Q8TAI1 Human Unigene: 723326 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications |
编码300个基因，18号染色体含有约7600万个碱基。Trisomy 18或爱德华兹综合征是唐氏综合征后第二常见的三体性疾病。爱德华兹综合征的症状包括低出生体重、多种身体发育缺陷、心脏畸形和呼吸困难。染色体18和14之间的易位是癌症中最常见的易位，并发生在滤泡性淋巴瘤中。尼曼匹克病、遗传性出血性毛细血管扩张症和红细胞生成性原卟啉症与第18号染色体有关。TGF-β调节剂、Smad2、Smad4和Smad7由18号染色体编码。C18ORF56基因产物已暂时指定为C18ORF56，有待进一步鉴定。