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- Bioss
- bs-17846R-HRP
- 2025年10月15日
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100ul
| 产品编号 | bs-17846R-HRP |
| 英文名称 | MSANTD2/C11orf61 Rabbit pAb, HRP conjugated |
| 中文名称 | HRP标记的11号染色体开放阅读框61抗体 |
| 英文别名 | C11orf61; CK061_HUMAN; FLJ23342; MSANTD2; Myb/SANT like DNA binding domain containing 2; Myb/SANT like DNA binding domain containing protein 2; Uncharacterized protein C11orf61. |
| 产品应用 | IHC-P=1:100-500, IHC-F=1:100-500 Not yet tested in other applications. |
| 抗体来源 | Rabbit |
| 免疫原 | KLH conjugated synthetic peptide derived from human MSANTD2/C11orf61 |
| 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 | Cell Biology > Other Antibodies > Other Antibodies |
| 相似性 | Contains 1 Myb-like domain. |
| 保存条件 | Shipped at 4℃. Store at -20°C for one year. Avoid repeated freeze/thaw cycles. |
| 背景资料 | C11orf61 is a 559 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and β thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11. |
| 应用 | 推荐稀释比例 |
| {IHC-P} | {1:100-500} |
| {IHC-F} | {1:100-500} |
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MSANTD2/C11orf61 Rabbit pAb, HRP conjugated(bs-17846R-HRP)-100ul
￥2980
