FITC标记的X染色体开放阅读框31抗体
产品名称： FITC标记的X染色体开放阅读框31抗体
英文名称： Anti-CXorf31/FITC
产品编号： HZ-14116R-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-CXorf31/FITC Conjugated antibody
FITC标记的X染色体开放阅读框31抗体
| 英文名称 | Anti-CXorf31/FITC |
| 中文名称 | FITC标记的X染色体开放阅读框31抗体 |
| 别 名 | Chromosome X open reading frame 31; CXorf31; Putative uncharacterized protein CXorf31; CX031_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 发育生物学 |
| 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 | 9.5kDa |
| 性 状 | Lyophilized or Liquid |
| 浓 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from human CXorf31 |
| 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 X and Y chromosomes are the human sex chromosomes. Chromosome X 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. The CXorf31 gene product has been provisionally designated CXorf31 pending further characterization. Database links: Entrez Gene: 724087 Human SwissProt: Q5VT33 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications |
X染色体和Y染色体是人类性染色体。X染色体由约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、血友病和杜氏肌营养不良是众所周知的X染色体连锁疾病，当男性携带单个X染色体时，这些疾病更频繁地影响男性。CXORF基因产物