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- Bioss
- bs-18550R-BF488
- 2025年09月30日
- 产品信息以Bioss网站为准
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- 规格：
100ul
| 产品编号 | bs-18550R-BF488 |
| 英文名称 | ZCCHC2 Rabbit pAb, BF488 conjugated |
| 中文名称 | BF488标记的ZCCHC2蛋白抗体 |
| 英文别名 | 9930114B20Rik; AW212015; DKFZp451A185; FLJ20281; KIAA1744; MGC112793; MGC13269; ZCCHC2; ZCHC2_HUMAN; Zinc finger CCHC domain containing protein 2; Zinc finger CCHC domain-containing protein 2. |
| 产品应用 | ICC/IF=1:50-200, 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 ZCCHC2 |
| 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. |
| 研究领域 | Epigenetics and Nuclear Signaling > Chromatin Binding Proteins > DNA / RNA binding |
| 相似性 | Contains 1 CCHC-type zinc finger. |
| 保存条件 | Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles. |
| 背景资料 | ZCCHC2 is a 1178 amino acid protein that contains one CCHC-type zinc finger, suggesting a role in transcriptional regulation. The gene encoding ZCCHC10 maps to human chromosome 18, which encodes over 300 genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, and erythropoietic protoporphyria. Translocation between chromosome 18 and 14 is also the most common translocation in cancers and occurs in follicular lymphomas. |
| 应用 | 推荐稀释比例 |
| {ICC/IF} | {1:50-200} |
| {IF} | {1:100-500} |
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ZCCHC2 Rabbit pAb, BF488 conjugated(bs-18550R-BF488)-100ul
￥2980
