Pola1 (NM_008892) Mouse Tagged ORF Clone Lentiviral Particle
CAT#: MR226939L4V
- LentiORF®
Lenti ORF particles, Pola1 (GFP-tagged) - Mouse polymerase (DNA directed), alpha 1 (Pola1), 200ul, >10^7 TU/mL
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CNY 22,705.00
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Specifications
Product Data | |
Product Name | Pola1 (NM_008892) Mouse Tagged ORF Clone Lentiviral Particle |
Synonyms | AW321876; Pola |
Vector | pLenti-C-mGFP-P2A-Puro |
ACCN | NM_008892 |
ORF Size | 4395 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(MR226939).
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OTI Disclaimer | The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info |
OTI Annotation | This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene. |
Reference Data | |
RefSeq | NM_008892.2, NP_032918.1 |
RefSeq Size | 5350 bp |
RefSeq ORF | 4398 bp |
Locus ID | 18968 |
Gene Summary | Plays an essential role in the initiation of DNA replication. During the S phase of the cell cycle, the DNA polymerase alpha complex (composed of a catalytic subunit POLA1/p180, a regulatory subunit POLA2/p70 and two primase subunits PRIM1/p49 and PRIM2/p58) 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. The reason this transfer occurs is because the polymerase alpha has limited processivity and lacks intrinsic 3' exonuclease activity for proofreading error, and therefore is not well suited for replicating long complexes. In the cytosol, responsible for a substantial proportion of the physiological concentration of cytosolic RNA:DNA hybrids, which are necessary to prevent spontaneous activation of type I interferon responses.[UniProtKB/Swiss-Prot Function] |
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