当前位置:首页>产品中心>单抗/多抗>Anti-Human MMS19 Polyclonal Antibody|抗人MMS19多克隆抗体(靶标:人MMS19核苷酸切除修复蛋白)

Anti-Human MMS19 Polyclonal Antibody|抗人MMS19多克隆抗体(靶标:人MMS19核苷酸切除修复蛋白)

  • 货号:RB9THC187014
  • 价格:面议
  • 点击:824
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产品介绍

产品参数

形态Liquid
宿主种属Rabbit
克隆性Polyclonal
抗体亚型IgG
纯化方式Purified by antigen affinity column.
内毒素水平Please contact with the lab for this information.
应用ELISA, IHC, WB
种属反应性Human, Mouse
靶标MET18 homolog, MMS19, MMS19 nucleotide excision repair protein homolog, MMS19-like protein, MMS19L, hMMS19
免疫原E. coli - derived recombinant Human MMS19 (Cys924-Ser1030).
储存缓冲液0.01M PBS, pH 7.4, 50% Glycerol, 0.05% Proclin 300.
产品使用说明ELISA:1:5000-1:20000;IHC:1:50-1:500;WB:1:500-1:2000
登录号Q96T76
背景信息

MMS19 nucleotide excision repair protein homolog is a ~113 kDa protein. Key component of the cytosolic iron-sulfur protein assembly (CIA) complex, a multiprotein complex that mediates the incorporation of iron-sulfur cluster into apoproteins specifically involved in DNA metabolism and genomic integrity. In the CIA complex, MMS19 acts as an adapter between early-acting CIA components and a subset of cellular target iron-sulfur proteins such as ERCC2/XPD, FANCJ and RTEL1, thereby playing a key role in nucleotide excision repair (NER), homologous recombination-mediated double-strand break DNA repair, DNA replication and RNA polymerase II (POL II) transcription. As part of the mitotic spindle-associated MMXD complex, plays a role in chromosome segregation, probably by facilitating iron-sulfur (Fe-S) cluster assembly into ERCC2/XPD. Together with CIAO2, facilitates the transfer of Fe-S clusters to the motor protein KIF4A, which ensures proper localization of KIF4A to mitotic machinery components to promote the progression of mitosis. Indirectly acts as a transcriptional coactivator of estrogen receptor (ER), via its role in iron-sulfur insertion into some component of the TFIIH-machinery.

1. Ben-Shimon, L. et al. (2018) Journal of cell science 131. PMID: 29848660
2. Gari, K. et al. (2012) Science (New York, N.Y.) 337, 243-5. PMID: 22678361
3. Stehling, O. et al. (2012) Science (New York, N.Y.) 337, 195-9. PMID: 22678362
4. Seki, M. et al. (2013) The Journal of biological chemistry 288, 16680-16689. PMID: 23585563
5. Weon, JL. et al. (2018) Molecular cell 69, 113-125.e6. PMID: 29225034
6. Ito, S. et al. (2010) Molecular cell 39, 632-40. PMID: 20797633
7. Wu, X. et al. (2001) The Journal of biological chemistry 276, 23962-8. PMID: 11279242
备注For research use only
【仅供科学研究使用】

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