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Anti-PINK1 Polyclonal Antibody (HV786014)

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概要
カタログ番号HV786014
説明
Anti-PINK1 Polyclonal Antibody (HV786014) is a rabbit polyclonal antibody detecting PINK1 in WB, IHC, ELISA. Suitable for Human, Mouse, Dog, Cat, and Bovine.
Highlights
  • ●Affinity Purified — Minimal background and high purity for reliable results.
  • ●Multi-Application — Validated across multiple applications.
  • ●Multi-Species — Cross-reactive for translational research.
種反応性Human
アプリケーションWB,IHC,ELISA
宿主種Rabbit
クローン性Polyclonal
アイソタイプIgG
ターゲット PINK1
エンドトキシンレベル Please contact with the lab for this information.
純度 >90% as determined by SDS-PAGE.
精製 Purified by antigen affinity column.
アクセッション番号 Q9BXM7
形態 Liquid
保存バッファー 0.01M PBS, pH 7.4, 50% Glycerol, 0.05% Proclin 300.

データシートのハードコピーまたはロット固有のCOAに記載された具体的なバッファー情報を参照してください。

製品使用情報
アプリケーション 希釈
ELISA 1:5000-1:20000
IHC 1:50-1:500
WB 1:500-1:2000
安定性と保存 Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
別名Serine/threonine-protein kinase PINK1 mitochondrial, EC:2.7.11.1, BRPK, PTEN-induced putative kinase protein 1, PINK1
背景

Serine/threonine-protein kinase PINK1, mitochondrial is a ~62 kDa protein. Serine/threonine-protein kinase which acts as a sensor of mitochondrial damage and protects against mitochondrial dysfunction during cellular stress. It phosphorylates mitochondrial proteins to coordinate mitochondrial quality control mechanisms that remove and replace dysfunctional mitochondrial components. In healthy mitochondria, PINK1 is translocated across the mitochondrial outer membrane (MOM) via the translocase of the outer membrane (TOM) complex, and inserted into the mitochondrial inner membrane (MIM) via the translocase of the inner membrane (TIM23) complex where it is cleaved and released into the cytosol. Depending on the severity of mitochondrial damage, activity ranges from preventing apoptosis and stimulating mitochondrial biogenesis to eliminating severely damaged mitochondria via PINK1-PRKN-dependent mitophagy. When cellular stress results in irreversible mitochondrial damage, PINK1 accumulates at the outer mitochondrial membrane (OMM) where it phosphorylates pre-existing polyubiquitin chains at 'Ser-65', recruits PRKN from the cytosol to the OMM and activates PRKN by phosphorylation at 'Ser-65'; activated PRKN then ubiquitinates VDAC1 and other OMM proteins to initiate mitophagy.

1. Callegari, S. et al. (2025) Science (New York, N.Y.) 388, 303-310. PMID: 40080546
2. Nakajima, A. et al. (2003) Cancer letters 201, 195-201. PMID: 14607334
3. Valente, EM. et al. (2004) Science (New York, N.Y.) 304, 1158-60. PMID: 15087508
4. Yang, Y. et al. (2008) Proceedings of the National Academy of Sciences of the United States of America 105, 7070-5. PMID: 18443288
5. Kim, Y. et al. (2008) Biochemical and biophysical research communications 377, 975-80. PMID: 18957282
6. Xiong, H. et al. (2009) The Journal of clinical investigation 119, 650-60. PMID: 19229105
7. Vives-Bauza, C. et al. (2010) Proceedings of the National Academy of Sciences of the United States of America 107, 378-83. PMID: 19966284
8. Matsuda, N. et al. (2010) The Journal of cell biology 189, 211-21. PMID: 20404107
9. Yuan, XL. et al. (2010) Brain research 1351, 229-237. PMID: 20547144
10. Geisler, S. et al. (2010) Autophagy 6, 871-8. PMID: 20798600
注意事項 For research use only.
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