产品中心
当前位置：首页>产品中心Anti-C2orf24/RBITC
货号： bs-9804R-RBITC 基本售价： 2980.0 元 规格： 100ul
产品信息
- 产品编号
- bs-9804R-RBITC
- 英文名称
- Anti-C2orf24/RBITC
- 中文名称
- 罗丹明（RBITC）标记的2号染色体开放阅读框24抗体
- 别 名
- CDABP0125; CGI 57; chromosome 2 open reading frame 24; CNPD1_HUMAN; CNPPD1; Cyclin Pas1/PHO80 domain-containing protein 1; Protein CNPPD1.
- 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
- 抗体来源
- Rabbit
- 克隆类型
- Polyclonal
- 交叉反应
- Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, 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
- 45kDa
- 性 状
- Lyophilized or Liquid
- 浓 度
- 1mg/ml
- 免 疫 原
- KLH conjugated synthetic peptide derived from human C2orf24
- 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 癈 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癈. 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 癈.
- 产品介绍
- background:
The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr鰉 syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes. The C2orf24 gene product has been provisionally designated C2orf24 pending further characterization.
Subcellular Location:
Membrane; Single-pass membrane protein (Potential).
Similarity:
Belongs to the CNPPD1 family.
Database links:Entrez Gene: 27013 Human
Entrez Gene: 69171 Mouse
Entrez Gene: 316530 Rat
SwissProt: Q5E9J2 Cow
SwissProt: Q9BV87 Human
SwissProt: Q8K158 Mouse
SwissProt: Q6P7B2 Rat
Unigene: 4973 Human
Unigene: 28193 Mouse
Unigene: 101111 Rat
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.