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货号： bs-8180R-PE-Cy3 基本售价： 2980.0 元 规格： 100ul
产品信息
- 产品编号
- bs-8180R-PE-Cy3
- 英文名称
- Anti-COMMD9/PE-Cy3
- 中文名称
- PE-Cy3标记的铜代谢结构域蛋白9抗体
- 别 名
- COMD9_HUMAN; COMM domain-containing protein 9; COMMD9; HSPC166.
- 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 通道蛋白
- 抗体来源
- Rabbit
- 克隆类型
- Polyclonal
- 交叉反应
- Human, Mouse, Rat, Dog, Pig, Cow, Sheep,
- 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
- 22kDa
- 性 状
- Lyophilized or Liquid
- 浓 度
- 1mg/ml
- 免 疫 原
- KLH conjugated synthetic peptide derived from human COMMD9
- 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:
COMMD9 (COMM domain containing 9) is a 198 amino acid ubiquitously expressed protein that contains one COMM domain and may be involved in signaling events throughout the cell. The gene encoding COMMD9 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
Tissue Specificity:
Ubiquitous.
Similarity:
Contains 1 COMM domain.
Database links:Entrez Gene: 29099Human
Omim: 612299Human
SwissProt: Q9P000Human
Unigene: 279836Human
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.