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- Bioss
- bs-17008R-HRP
- 2025年09月30日
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100ul
| 产品编号 | bs-17008R-HRP |
| 英文名称 | KIAA1467 Rabbit pAb, HRP conjugated |
| 中文名称 | HRP标记的KIAA1467蛋白抗体 |
| 英文别名 | Uncharacterized protein KIAA1467; K1467_HUMAN. |
| 产品应用 | WB=1:500-2000 Not yet tested in other applications. |
| 抗体来源 | Rabbit |
| 免疫原 | KLH conjugated synthetic peptide derived from human KIAA1467 |
| 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 | Membrane; Single pass membrane protein |
| 相似性 | Belongs to the ITFG3 family. |
| 保存条件 | Shipped at 4℃. Store at -20°C for one year. Avoid repeated freeze/thaw cycles. |
| 注意事项 | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| 背景资料 | KIAA1467 is a 622 amino acid single-pass membrane protein that belongs to the ITFG3 family. KIAA1467 is post-translationally phosphorylated at multiple serine residues and tyrosine 22. The gene encoding KIAA1467 maps to human chromosome 12, which encodes over 1,100 genes and comprises about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster, which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster, encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms which vary in severity depending on the extent of mosaicism. It is most severe in cases of complete trisomy. |
| 应用 | 推荐稀释比例 |
| {WB} | {1:500-2000} |
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KIAA1467 Rabbit pAb, HRP conjugated(bs-17008R-HRP)-100ul
￥2980
