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- Bioss
- bs-13757R-BF750
- 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-13757R-BF750 |
| 英文名称 | C1orf158 Rabbit pAb, BF750 conjugated |
| 中文名称 | BF750标记的1号染色体开放阅读框58抗体 |
| 英文别名 | C1orf158; CA158_HUMAN; Chromosome 1 open reading frame 158; RP11-474O21.4; Uncharacterized protein C1orf158. |
| 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 C1orf158 |
| 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 | Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf158 gene product has been provisionally designated C1orf158 pending further characterization. |
| 应用 | 推荐稀释比例 |
| {IF} | {1:100-500} |
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C1orf158 Rabbit pAb, BF750 conjugated(bs-13757R-BF750)-100ul
￥2980
