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- 技术资料
- 规格:
500ug
| 产品编号 | bs-9934P |
| 英文名称 | HARBI1 Antibody Blocking Peptide |
| 中文名称 | 11号染色体开放阅读框77封闭多肽 |
| 英文别名 | Chromosome 11 open reading frame 77; FLJ32675; HARB1_HUMAN; HARBI1; Harbinger transposase derived 1; Harbinger transposase-derived nuclease; Putative nuclease HARBI1. |
| 纯化方法 | HPLC |
| 亚基 | Interacts with NAIF1. |
| 亚细胞定位 | Nucleus. Cytoplasm. Interaction with NAIF1 promotes translocation to the nucleus. |
| 组织特异性 | Detected in brain, eye, nerve tissue, kidney and lung. |
| 相似性 | Belongs to the HARBI1 family. |
| 功能 | Transposase-derived protein that may have nuclease activity (Potential). Does not have transposase activity. |
| 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 | HARBI1 is a 349 amino acid nuclear and cytoplasmic protein belonging to the HARBI1 family. Members of the HARBI1 family of proteins are highly conserved in humans to various bony fish. Considered a transposase-derived protein, HARBI1 may possess nuclease activity and is expressed in brain, eye, nerve tissue, kidney and lung. HARBI1 utilizes divalent metal cations as cofactors, interacts with NAIF1 and promotes translocation to the nucleus. HARBI1 is encoded by a gene located on human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11. |
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HARBI1 Antibody Blocking Peptide(bs-9934P)-500ug
¥880







