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- Bioss
- bs-16011R-AP
- 2025年09月30日
- 产品信息以Bioss网站为准
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产品信息以Bioss网站为准
- 规格：
100ul
| 产品编号 | bs-16011R-AP |
| 英文名称 | FAM73B Rabbit pAb, AP conjugated |
| 中文名称 | AP标记的FAM73B蛋白抗体 |
| 英文别名 | C9orf54; FA73B_HUMAN; Fam73b; Family with sequence similarity 73, member B; FLJ00199; FLJ14596; Protein FAM73B; RP11-167N5.1. |
| 产品应用 | WB=1:500-2000 Not yet tested in other applications. |
| 抗体来源 | Rabbit |
| 免疫原 | KLH conjugated synthetic peptide derived from human FAM73B |
| 亚型 | IgG |
| 纯化方法 | affinity purified by Protein A |
| 克隆类型 | Polyclonal |
| 浓度 | 1mg/ml |
| 储存液 | 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. |
| 亚细胞定位 | Membrane. |
| 相似性 | Belongs to the FAM73 family. |
| 保存条件 | Shipped at 4℃. Store at -20°C for one year. Avoid repeated freeze/thaw cycles. |
| 注意事项 | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| 背景资料 | Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The FAM73B gene product has been provisionally designated FAM73B pending further characterization. |
| 应用 | 推荐稀释比例 |
| {WB} | {1:500-2000} |
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FAM73B Rabbit pAb, AP conjugated(bs-16011R-AP)-100ul
￥2980
