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货号： bs-15284R-PE-Cy7 基本售价： 2980.0 元 规格： 100ul
产品信息
- 产品编号
- bs-15284R-PE-Cy7
- 英文名称
- Anti-C8orf30A/PE-Cy7
- 中文名称
- PE-Cy7标记的8号染色体开放阅读框30a抗体
- 别 名
- Brain protein 16; BRP16; chromosome 8 open reading frame 30A; D15Ertd741e; F203A_HUMAN; Fam203a; FLJ40907; LOC51236; MGC94185; MNCb-5873; Protein FAM203A.
- 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, Dog, Pig, Cow, Sheep,
- 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
- 42kDa
- 性 状
- Lyophilized or Liquid
- 浓 度
- 1mg/ml
- 免 疫 原
- KLH conjugated synthetic peptide derived from human C8orf30A
- 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:
Brp16 is a 256 amino acid protein encoded by a gene on human chromosome 8. Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome.
Similarity:
Belongs to the FAM203 family.
Database links:Entrez Gene: 51236Human
Entrez Gene: 728071Human
Entrez Gene: 59053Mouse
Entrez Gene: 315094Rat
SwissProt: Q9BTY7Human
SwissProt: Q8C3I8Mouse
SwissProt: Q6AY79Rat
Unigene: 300224Human
Unigene: 133202Mouse
Unigene: 17102Rat
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.