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- Bioss
- bs-15179R-APC
- 2025年09月30日
- 产品信息以Bioss网站为准
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100ul
| 产品编号 | bs-15179R-APC |
| 英文名称 | C3orf58 Rabbit pAb, APC conjugated |
| 中文名称 | APC标记的3号染色体开放阅读框58抗体 |
| 英文别名 | Chromosome 3 open reading frame 58; DIA1; Golgi protein GoPro49; MGC33365; UPF0672 protein C3orf58; DIA1_HUMAN. |
| 产品应用 | IF=1:100-500 Not yet tested in other applications. |
| 抗体来源 | Rabbit |
| 免疫原 | KLH conjugated synthetic peptide derived from human C3orf58 |
| 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. |
| 保存条件 | Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles. |
| 背景资料 | C3orf58 (chromosome 3 open reading frame 58), also known as DIA1, is a 430 amino acid secreted protein that belongs to the UPF0672 family. C3orf58 is encoded by a gene that maps to human chromosome 3q24. Chromosome 3 is made up of approximately 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth disease are a few of the numerous genetic diseases associated with chromosome 3. |
| 应用 | 推荐稀释比例 |
| {IF} | {1:100-500} |
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C3orf58 Rabbit pAb, APC conjugated(bs-15179R-APC)-100ul
￥2980
