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- Bioss
- bs-12381P
- 2025年10月16日
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- 规格：
500ug
| 产品编号 | bs-12381P |
| 英文名称 | CAMSAP1 Antibody Blocking Peptide |
| 中文名称 | 钙调素调节蛋白相关蛋白封闭多肽 |
| 英文别名 | calmodulin regulated spectrin-associated protein 1; Calmodulin-regulated spectrin-associated protein 1; CAMP1_HUMAN; camsap1; PRO2405. |
| 纯化方法 | HPLC |
| 研究领域 | Stem Cells > Neural Stem Cells > Glial Restricted Lineage > Astrocyte |
| 亚细胞定位 | Cytoplasm; cytoskeleton. |
| 相似性 | Belongs to the CAMSAP1 family. Contains 1 CH (calponin-homology) domain. Contains 1 CKK domain. |
| 功能 | Plays a role in the regulation of cell morphology and cytoskeletal organization. |
| 保存条件 | Shipped at 4℃. Stored at -20℃ 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 | CAMSAP1L1 is a 1,489 amino acid protein that contains one calponin-homology domain and one CKK domain, which serves to bind microtubules. There are three isoforms of CAMSAP1L1 that are produced as a result of alternative splicing events. The gene encoding CAMSAP1L1 maps to human chromosome 1, the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. |
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CAMSAP1 Antibody Blocking Peptide(bs-12381P)-500ug
￥880
