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- bs-8578R-RBITC
- 2025年09月30日
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100ul
| 产品编号 | bs-8578R-RBITC |
| 英文名称 | GRAMD2 Rabbit pAb, RBITC conjugated |
| 中文名称 | RBITC标记的GRAM结构域蛋白2抗体 |
| 英文别名 | GRAM domain containing 2; GRAM domain containing protein 2; GRAMD 2; GRAM2_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 GRAMD2 |
| 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 |
| 亚细胞定位 | Membrane; Single-pass membrane protein (Potential). |
| 相似性 | Contains 1 GRAM domain._x000D_ |
| 保存条件 | Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles. |
| 背景资料 | GRAMD2 is a 354 amino acid single-pass membrane protein that contains one GRAM domain and is encoded by a gene that maps to human chromosome 15q23. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. |
| 应用 | 推荐稀释比例 |
| {IF} | {1:100-500} |
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GRAMD2 Rabbit pAb, RBITC conjugated(bs-8578R-RBITC)-100ul
￥2980
