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货号： bs-8196R-AF555 基本售价： 2980.0 元 规格： 100ul
产品信息
- 产品编号
- bs-8196R-AF555
- 英文名称
- Anti-FAM55D/AF555
- 中文名称
- AF555标记的FAM55D蛋白抗体
- 别 名
- C11orf33; Chromosome 11 open reading frame 33; FA55D_HUMAN; Fam55d; Family with sequence similarity 55 member D; Family with sequence similarity 55, member D; FLJ20127; Hypothetical protein LOC54827; Protein FAM55D.
- 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,
- 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
- 59kDa
- 性 状
- Lyophilized or Liquid
- 浓 度
- 1mg/ml
- 免 疫 原
- KLH conjugated synthetic peptide derived from human FAM55D
- 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:
FAM55D is a 544 amino acid secreted protein that is expressed as two isoforms due to alternative splicing events. The gene encoding FAM55D is located on chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. Wilms tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11. The FAM55D gene product has been provisionally designated FAM55D pending further characterization.
Subcellular Location:
Secreted (Potential).
Similarity:
Belongs to the NXPE family.
Database links:Entrez Gene: 54827Human
Entrez Gene: 244853Mouse
Entrez Gene: 500991Rat
SwissProt: Q6UWF7Human
SwissProt: Q52KP5Mouse
SwissProt: Q5XI89Rat
Unigene: 179100Human
Unigene: 325522Mouse
Unigene: 29872Rat
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.