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Human PRIM1 Recombinant Protein (N-His) (HD045012)

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概要
カタログ番号HD045012
説明
Recombinant Human PRIM1 Protein, N-His (HD045012) expressed in E. coli, spanning Met1-Phe420. Purity: >90% by SDS-PAGE.
Highlights
  • ●His-Tagged — N-terminal 6×His tag for IMAC purification.
  • ●E. coli Expression — High-yield, cost-effective production.
  • ●High Purity — >90% purity verified by SDS-PAGE.
発現システムE. coli
アクセッション番号P49642
タンパク質長Met1-Phe420
アプリケーションELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
種Homo sapiens (Human)
性質 Recombinant
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.
予測分子量 52.06 kDa
形態 Lyophilized
保存バッファー Lyophilized from a solution in PBS pH 7.4, 1 mM EDTA, 4% Trehalose, 1% Mannitol.

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。

再構成 Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.
発送 In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.
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DNA primase 49 kDa subunit, DNA primase small subunit, EC:2.7.7.102, PRIM1, p49
背景

DNA primase small subunit is a ~49 kDa protein. Catalytic subunit of the DNA primase complex and component of the DNA polymerase alpha complex (also known as the alpha DNA polymerase-primase complex - primosome/replisome) which play an essential role in the initiation of DNA synthesis. During the S phase of the cell cycle, the DNA polymerase alpha complex (composed of a catalytic subunit POLA1, an accessory subunit POLA2 and two primase subunits, the catalytic subunit PRIM1 and the regulatory subunit PRIM2) is recruited to DNA at the replicative forks via direct interactions with MCM10 and WDHD1. The primase subunit of the polymerase alpha complex initiates DNA synthesis by oligomerising short RNA primers on both leading and lagging strands. These primers are initially extended by the polymerase alpha catalytic subunit and subsequently transferred to polymerase delta and polymerase epsilon for processive synthesis on the lagging and leading strand, respectively. In the primase complex, both subunits are necessary for the initial di-nucleotide formation, but the extension of the primer depends only on the catalytic subunit.

1. Weiner, BE. et al. (2007) The Journal of biological chemistry 282, 33444-33451. PMID: 17893144
2. Kilkenny, ML. et al. (2013) Proceedings of the National Academy of Sciences of the United States of America 110, 15961-6. PMID: 24043831
3. Baranovskiy, AG. et al. (2015) The Journal of biological chemistry 290, 5635-46. PMID: 25550159
4. Baranovskiy, AG. et al. (2016) The Journal of biological chemistry 291, 10006-20. PMID: 26975377
5. Holzer, S. et al. (2019) ACS chemical biology 14, 1904-1912. PMID: 31479243
6. Parry, DA. et al. (2020) Genes & development 34, 1520-1533. PMID: 33060134
7. Cloutier, S. et al. (1997) Genomics 43, 398-401. PMID: 9268648
8. Schneider, A. et al. (1998) The Journal of biological chemistry 273, 21608-15. PMID: 9705292
注意事項 For research use only
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参考文献
Formula
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