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- 详细信息
- 文献和实验
- 技术资料
- 免疫原:
Recombinant full length protein (coding region) of Tom9.2 Arabidopsis thaliana UniProt: Q9FNC9 TAIR: AT5G43970
- 形态:
Lyophilized
- 保存条件:
Store lyophilized/reconstituted at -20°C; once rec
- 克隆性:
Polyclonal
- 标记物:
Kolodziejczak et al. (2018). m-AAA Complexes Are Not Crucial for the Survival of Arabidopsis Under Optimal Growth Conditions Despite Their Importance for Mitochondrial Translation. Plant Cell Physiol. 2018 May 1;59(5):1006-1016. doi: 10.1093/pcp/pcy041.
- 适应物种:
Arabidopsis thaliana
- 抗原来源:
Q9FNC9
- 级别:
分子生物学级
- 供应商:
Agrisera
- 宿主:
Rabbit
- 应用范围:
1 : 1000 (WB)
- 靶点:
TOM9 (Mitochondrial import receptor subunit TOM9) is a central component of the receptor complex responsible for recognition and translocation of cytosolically synthesized mitochondrial preproteins. Alternative names: Mitochondrial import receptor subunit
- 抗体英文名:
Antibody works on whole leaf extracts and isolated mitochondria; requires Tricine gels for sharp bands due to the small MW.
- 抗体名:
Tom 9.2 | Mitochondrial import receptor subunit TOM9.2
- 规格:
50 µl
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文献和实验Identification of Mutations in the Kir6.2 Subunit of the KATP Channel
of the sulfonylurea receptor 1. Loss of function mutations in the KCNJ11 and ABCC8 genes that encode for Kir6.2 and SUR1 can cause over-secretion of insulin and result in hyperinsulinism of infancy, while gain of function mutations in KCNJ11 and ABCC8 have recently
Using Hidden Markov Models to Discover New Protein Transport Machines
and is initiated when substrate proteins are translocated across the mitochondrial outer membrane by the TOM complex. The essential subunit of this complex is a protein called Tom40, which is probably a β-barrel in structure and serves as the translocation pore
Real‐Time Quantitative PCR Analysis of Mitochondrial DNA Content
., Christensen, E., Kristensen, E., Mogensen, B., Duno, M., Shoubridge, E.A., and Wibrand, F. 2007b. Deficiency of the alpha subunit of succinate‐coenzyme A ligase causes fatal infantile lactic acidosis with mitochondrial DNA depletion. Am. J. Hum. Genet. 81:383
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