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- 2025年10月16日
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500ug
| 产品编号 | bs-16200P |
| 英文名称 | TIMM10B Antibody Blocking Peptide |
| 中文名称 | 骨折骨痂蛋白1封闭多肽 |
| 英文别名 | Fracture callus 1 homolog (rat); Fracture callus protein 1; FxC1; Mitochondrial import inner membrane translocase subunit Tim9 B; OTTHUMP00000164584; OTTHUMP00000230720; TIM 10B; Tim10b; Tim9b; T10B_HUMAN; TIMM10B. |
| 纯化方法 | HPLC |
| 亚基 | Component of the TIM22 complex, whose core is composed of TIMM22, associated with peripheral protein TIMM10B/FXC1 and the 70 kDa heterohexamer. In most cases, the 70 kDa complex is composed of TIMM9 and TIMM10. Also forms a complex composed of TIMM9, TIMM10/TIM10A and TIMM10B/FXC1. |
| 亚细胞定位 | Mitochondrion inner membrane. |
| 组织特异性 | Ubiquitous, with highest expression in heart, kidney, liver and skeletal muscle. |
| 相似性 | Belongs to the small Tim family. |
| 功能 | Component of the TIM22 complex, a complex that mediates the import and insertion of multi-pass transmembrane proteins into the mitochondrial inner membrane. The TIM22 complex forms a twin-pore translocase that uses the membrane potential as external driving force. In the TIM22 complex, it may act as a docking point for the soluble 70 kDa complex that guides the target proteins in transit through the aqueous mitochondrial intermembrane space. |
| 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 | FXC1, or TIMM10B, belongs to a family of evolutionarily conserved proteins that are organized in heterooligomeric complexes in the mitochondrial intermembrane space. These proteins mediate the import and insertion of hydrophobic membrane proteins into the mitochondrial inner membrane.[supplied by OMIM, Apr 2004] |
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文献和实验Blocking of unwanted non-specific staining
by acting on primary Abs. 5- Wash once in TBS-T (residual milk can contribute to blocking). Blocking of endogenous Fc blocking. Specimens not paraffin embeddded may have significant Fc binding activity by macrophages, B cells, T cells
Antibody Signatures Defined by High-Content Peptide Microarray Analysis
from clinically well-defined patient populations. The methodology is robust and enables unbiased visualization of antigen-specific B-cell responses. Additionally, autoantibody signatures of diagnostic value could be detected using microarrays displaying thousands
or from the literature are missing. In this article, processing parameters for DNA, peptide, antibody, and carbohydrate microarrays are outlined. The applicability of the model experiments is demonstrated and described in detail on the example of short oligonucleotides.
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