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Anti-SARS1 Polyclonal Antibody (HA659014)

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概要
カタログ番号HA659014
説明
Anti-SARS1 Polyclonal Antibody (HA659014) is a rabbit polyclonal antibody detecting cytoplasmic; 6.1.1.11; Seryl-tRNA synthetase; SerRS; Seryl-tRNA(Ser/Sec) synthetase; SARS1; SARS; SERS in ELISA, IHC, WB. Suitable for Human, Bovine, Rabbit, Mouse, and Rat.
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, Mouse, Rat
アプリケーションELISA, IHC, WB
宿主種Rabbit
クローン性Polyclonal
アイソタイプIgG
免疫原 E. coli - derived recombinant human SARS1 (Ser142-Lys472).
ターゲット Serine--tRNA ligase, cytoplasmic; 6.1.1.11; Seryl-tRNA synthetase; SerRS; Seryl-tRNA(Ser/Sec) synthetase; SARS1; SARS; SERS
エンドトキシンレベル Please contact with the lab for this information.
精製 Purified by antigen affinity column.
アクセッション番号 P49591, Q9GMB8, P13642, P26638, Q6P799, Q6DRC0
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.
背景

Serine--tRNA ligase, cytoplasmic (SARS1) is a ~58 kDa protein. Catalyzes the attachment of serine to tRNA(Ser) in a two-step reaction: serine is first activated by ATP to form Ser-AMP and then transferred to the acceptor end of tRNA(Ser). Is probably also able to aminoacylate tRNA(Sec) with serine, to form the misacylated tRNA L-seryl-tRNA(Sec), which will be further converted into selenocysteinyl-tRNA(Sec). In the nucleus, binds to the VEGFA core promoter and prevents MYC binding and transcriptional activation by MYC. Recruits SIRT2 to the VEGFA promoter, promoting deacetylation of histone H4 at 'Lys-16' (H4K16). Thereby, inhibits the production of VEGFA and sprouting angiogenesis mediated by VEGFA.

1. Xu, X. et al. (2012) Nature communications 3, 681. PMID: 22353712
2. Xu, X. et al. (2013) Structure (London, England : 1993) 21, 2078-86. PMID: 24095058
3. Wang, C. et al. (2015) Nucleic acids research 43, 10534-45. PMID: 26433229
4. Musante, L. et al. (2017) Human mutation 38, 621-636. PMID: 28236339
5. Ravel, JM. et al. (2021) Human mutation 42, 1576-1583. PMID: 34570399
6. Verdura, E. et al. (2022) Journal of medical genetics 59, 1227-1233. PMID: 36041817
7. Vincent, C. et al. (1997) European journal of biochemistry 250, 77-84. PMID: 9431993
8. Shi, Y. et al. (2014) eLife 3, e02349. PMID: 24940000
9. Herzog, W. et al. (2009) Circulation research 104, 1260-6. PMID: 19423847
10. Fukui, H. et al. (2009) Circulation research 104, 1253-9. PMID: 19423848
注意事項 For research use only
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