FITC标记的肿瘤/睾丸抗原47B1抗体
产品名称： FITC标记的肿瘤/睾丸抗原47B1抗体
英文名称： Anti-CT47B1/FITC
产品编号： HZ-14094R-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-CT47B1/FITC Conjugated antibody
FITC标记的肿瘤/睾丸抗原47B1抗体
| 英文名称 | Anti-CT47B1/FITC |
| 中文名称 | FITC标记的肿瘤/睾丸抗原47B1抗体 |
| 别 名 | cancer/testis antigen 47.13; cancer/testis antigen 47B; cancer/testis antigen family 47, member B1; cancer/testis CT47 family, member 13; CT47.13; CT47B_HUMAN; CT47A13. |
| 规格价格 | 100ul/2980元 购买 大包装/询价 |
| 说 明 书 | 100ul |
| 研究领域 | 肿瘤 免疫学 肿瘤细胞生物标志物 |
| 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 | 31kDa |
| 性 状 | Lyophilized or Liquid |
| 浓 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from human CT47B1 |
| 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: CT47 (cancer/testis antigen family 47) is a 288 amino acid protein that is strongly expressed in testis and lowly expressed in placenta and in brain. The gene encoding CT47 is located on human chromosome X, which consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome. Database links: Entrez Gene: 643311 Human Omim: 300790 Human SwissProt: P0C2W7 Human Unigene: 729566 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications |
CT47（癌/睾丸抗原家族47）是一种在睾丸中强烈表达并在胎盘和脑中低表达的288氨基酸蛋白。编码CT47的基因位于人类X染色体上，由约1亿5300万个碱基对和近1000个基因组成。X和Y染色体的组合导致正常的男性发育，而X的两个拷贝导致正常的女性发育。有许多条件与一个未成年的数量和性染色体的结合有关。X染色体Y染色体的一个以上拷贝引起Krimelelter综合征。单拷贝X导致Turnter综合征。在Y染色体缺失的情况下，X染色体的2个拷贝被称为三重X综合征。色盲、血友病和Duchenne型肌营养不良是众所周知的X染色体连锁的情况，这影响男性更频繁，因为男性携带单个X染色体。