- ￥880
- Bioss
- bs-15591P
- 2025年10月16日
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500ug
| 产品编号 | bs-15591P |
| 英文名称 | LETM1 Antibody Blocking Peptide |
| 中文名称 | LETM1蛋白封闭多肽 |
| 英文别名 | LETM 1; LETM1 and EF hand domain containing protein 1, mitochondrial; LETM1 and EF-hand domain-containing protein 1; Letm1; LETM1_HUMAN; Leucine zipper EF hand containing transmembrane protein 1; Leucine zipper-EF-hand-containing transmembrane protein 1; Mdm38 homolog; mitochondrial; ZNF300 bs-0628R |
| 纯化方法 | HPLC |
| 研究领域 | Metabolism > Pathways and Processes > Mitochondrial Metabolism > Mitochondrial Biogenesis Metabolism > Pathways and Processes > Mitochondrial Metabolism > Mitochondrial markers Tags & Cell Markers > Subcellular Markers > Organelles > Mitochondria |
| 亚基 | Can form 2 complexes: a major (300 kDa) and a minor complex (500-600 kDa). Interacts with BCS1L. |
| 亚细胞定位 | Mitochondrion inner membrane; Single-pass membrane protein. |
| 相似性 | Contains 1 EF-hand domain. Contains 1 LETM1 domain. |
| 功能 | Crucial for the maintenance of mitochondrial tubular networks and for the assembly of the supercomplexes of the respiratory chain. Required for the maintenance of the tubular shape and cristae 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 | This gene encodes a protein that is localized to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf-Hirschhorn syndrome, a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8, 15 and 19. [provided by RefSeq, Oct 2009]. |
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LETM1 Antibody Blocking Peptide(bs-15591P)-500ug
￥880
