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- Bioss
- bs-13791R-Cy5
- 2025年09月30日
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100ul
| 产品编号 | bs-13791R-Cy5 |
| 英文名称 | C19orf57 Rabbit pAb, Cy5 conjugated |
| 中文名称 | Cy5标记的19号染色体开放阅读框57抗体 |
| 英文别名 | C19orf57; CS057_HUMAN; Pre-T/NK cell-associated protein 3B3; Uncharacterized protein C19orf57. |
| 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 C19orf57 |
| 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. |
| 翻译后修饰 | Phosphorylated upon DNA damage, probably by ATM or ATR. |
| 保存条件 | Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles. |
| 背景资料 | C19orf57 is a 668 amino acid protein that exists as two alternatively spliced isoforms and are encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. |
| 应用 | 推荐稀释比例 |
| {IF} | {1:100-500} |
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C19orf57 Rabbit pAb, Cy5 conjugated(bs-13791R-Cy5)-100ul
￥2980
