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- Bioss
- bs-11003R-PerCP-Cy5.5
- 2025年09月30日
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100ul
| 产品编号 | bs-11003R-PerCP-Cy5.5 |
| 英文名称 | FAM62B Rabbit pAb, PerCP-Cy5.5 conjugated |
| 中文名称 | PerCP-Cy5.5标记的延伸突触蛋白2抗体 |
| 英文别名 | Chr2 synaptotagmin; CHR2SYT; E Syt2; ESYT 2; ESYT2; Extended synaptotagmin 2; Extended synaptotagmin like protein 2; FAM 62B antibody Family with sequence similarity 62(C2 domain containing) member B; Family with sequence similarity 62 member B; KIAA1228; Protein FAM62B; ESYT2_HUMAN. |
| 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 ESYT2/FAM62B |
| 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 | Cell membrane; Multi-pass membrane protein. |
| 组织特异性 | Widely expressed with high level in cerebellum. _x000D_ |
| 相似性 | Belongs to the extended synaptotagmin family. Contains 3 C2 domains. |
| 功能 | May play a role as calcium-regulated intrinsic membrane protein. _x000D_ _x000D_ |
| 保存条件 | Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles. |
| 背景资料 | Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up 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 varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The FAM62A gene product has been provisionally designated FAM62A pending further characterization. |
| 应用 | 推荐稀释比例 |
| {ICC/IF} | {1:50-200} |
| {IF} | {1:100-500} |
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FAM62B Rabbit pAb, PerCP-Cy5.5 conjugated(bs-11003R-PerCP-Cy5.5)-100ul
￥2980
