

| Numéro de catalogue | HA705014 | ||||||||
|---|---|---|---|---|---|---|---|---|---|
| Description |
Anti-PRIM2 Polyclonal Antibody (HA705014) is a rabbit polyclonal antibody detecting DNA primase large subunit; DNA primase 58 kDa subunit; p58; PRIM2; PRIM2A in ELISA, IHC, WB. Suitable for Human, Mouse, and Rat.
Highlights
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| Reactivité des espèces | Human | ||||||||
| Applications | ELISA, IHC, WB | ||||||||
| Espèce hôte | Rabbit | ||||||||
| Clonalité | Polyclonal | ||||||||
| Isotype | IgG | ||||||||
| Immunogène | E. coli - derived recombinant human PRIM2 (Thr264-Ser509). | ||||||||
| Cible | DNA primase large subunit; DNA primase 58 kDa subunit; p58; PRIM2; PRIM2A | ||||||||
| Niveau d'endotoxines | Please contact with the lab for this information. | ||||||||
| Purification | Purified by antigen affinity column. | ||||||||
| Numéro d'accès | P49643, P33610, O89044 | ||||||||
| Forme | Liquid | ||||||||
| Tampon de stockage | 0.01M PBS, pH 7.4, 50% Glycerol, 0.05% Proclin 300. Reférez-vous aux informations spécifiques sur le tampon dans la copie papier du datasheet ou dans le COA spécifique au lot. |
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| Informations d'utilisation du produit |
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| Stabilité et stockage | 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. | ||||||||
| Contexte | DNA primase large subunit (PRIM2) is a ~58 kDa protein. Regulatory subunit of the DNA primase complex and component of the DNA polymerase alpha complex (also known as the alpha DNA polymerase-primase complex) 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. Baranovskiy, AG. et al. (2015) The Journal of biological chemistry 290, 5635-46. PMID: 25550159 3. Baranovskiy, AG. et al. (2016) The Journal of biological chemistry 291, 10006-20. PMID: 26975377 4. Schneider, A. et al. (1998) The Journal of biological chemistry 273, 21608-15. PMID: 9705292 | ||||||||
| Note | For research use only |

Western blot analysis was performed using anti-PRIM2 polyclonal antibody at 1ug/mL on various samples.
Lane 1: 293T cell lysate
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