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- Bioss
- bs-13326R-RBITC
- 2025年09月30日
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100ul
| 产品编号 | bs-13326R-RBITC |
| 英文名称 | GDPGP1 Rabbit pAb, RBITC conjugated |
| 中文名称 | RBITC标记的15号染色体开放阅读框58抗体 |
| 英文别名 | C15orf58; Chromosome 15 open reading frame 58; GDP-D-glucose phosphorylase 1; GDP-D-glucose phosphorylase C15orf58; gdpgp1; GDPP1_HUMAN; VTC2. |
| 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 GDPGP1/C15orf58 |
| 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. |
| 亚细胞定位 | Cytoplasm. |
| 相似性 | Belongs to the GDPGP1 family. |
| 功能 | Specific and highly efficient GDP-D-glucose phosphorylase regulating the levels of GDP-D-glucose in cells. |
| 保存条件 | Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles. |
| 背景资料 | 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. The LOC390637 gene product has been provisionally designated LOC390637 pending further characterization. |
| 应用 | 推荐稀释比例 |
| {IF} | {1:100-500} |
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GDPGP1 Rabbit pAb, RBITC conjugated(bs-13326R-RBITC)-100ul
￥2980
