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货号： bs-0488R-PE-Cy7 基本售价： 2980.0 元 规格： 100ul
产品信息
- 产品编号
- bs-0488R-PE-Cy7
- 英文名称
- Anti-CXorf36/PE-Cy7
- 中文名称
- PE-Cy7标记的脱羧酶蛋白体36抗体
- 别 名
- chromosome X open reading frame 36, isoform CRA_a ; uncharacterized protein Cxorf36 precursor; PRO3743; EPQL1862; FLJ14103; FLJ55198; FLJ55198, bA435K1.1; 4930578C19Rik; DKFZp313K0825; CXorf36; DIA1R_HUMAN; DIA1R; PRO3743; EPQL1862; bA435K1.1; 4930578C19Rik.
- 规格价格
- 100ul/2980元购买 大包装/询价
- 说 明 书
- 100ul
- 研究领域
- 肿瘤
- 抗体来源
- Rabbit
- 克隆类型
- Polyclonal
- 交叉反应
- Human, Mouse, Rat, Dog, Cow,
- 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
- 20/45kDa
- 性 状
- Lyophilized or Liquid
- 浓 度
- 1mg/ml
- 免 疫 原
- KLH conjugated synthetic peptide derived from human CXorf36
- 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 Klinefelters syndrome. A single copy of X alone leads to Turners 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 CXorf36 gene product has been provisionally designated CXorf36 pending further characterization.
Subcellular Location:
Secreted (Potential).
DISEASE:
Note=Genetic variations in CXorf36 may be associated with susceptibility to autism.
Similarity:
Belongs to the DIA1 family.
Database links:Entrez Gene: 79742 Human
SwissProt: Q9H7Y0 Human
Unigene: 98321 Human
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
经研究：CXorf36蛋白是通过其水解酶活性，在肿瘤的发生、生长或侵袭过程中发挥重要作用。对关于CXorf36基因功能的研究,其在肿瘤组织中的定位、对细胞生物学功能的影响需进一步研究。
文献参考：肾癌相关基因CXorf36的克隆及亚定位研究