产品中心
当前位置:首页>产品中心Anti-N6AMT2/FITC
货号: bs-18988R-FITC 基本售价: 2980.0 元 规格: 100ul
产品信息
- 产品编号
- bs-18988R-FITC
- 英文名称
- Anti-N6AMT2/FITC
- 中文名称
- FITC标记的N6AMT2蛋白抗体
- 别 名
- ESP13; N 6 adenine specific DNA methyltransferase 2 (putative); N(6) adenine specific DNA methyltransferase 2; N(6)-adenine-specific DNA methyltransferase 2; N6AMT2; N6MT2_HUMAN.
- 规格价格
- 100ul/2980元购买 大包装/询价
- 说 明 书
- 100ul
- 研究领域
- 肿瘤 细胞生物 表观遗传学
- 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
- 25kDa
- 性 状
- Lyophilized or Liquid
- 浓 度
- 1mg/ml
- 免 疫 原
- KLH conjugated synthetic peptide derived from human N6AMT2
- 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:
N6AMT2 is a 214 amino acid protein that is encoded by a gene located on human chromosome 13q12.11. Comprising nearly 4% of the human genome, chromosome 13 contains around 114 million base pairs and encodes over 400 genes. Chromosome 13 houses key tumor suppressor genes, including BRCA2 and RB1, which are associated with breast cancer susceptibility and retinoblastoma, respectively. Trisomy 13, also known as Patau syndrome, is deadly and the few who survive past one year suffer from permanent neurologic defects, difficulty eating and vulnerability to serious respiratory infections
Function:
Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate
Subunit:
Alpha-D-glucosamine 1-phosphate = D-glucosamine 6-phosphate.
Post-translational modifications:
Activated by phosphorylation
Similarity:
Belongs to the phosphohexose mutase family.
Database links:Entrez Gene: 221143Human
SwissProt: Q8WVE0Human
Unigene: 26674Human
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.