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Anti-Gs protein, alpha subunit Recombinant Antibody (N192/12) (HY062013)

Anti-Gs protein, alpha subunit Recombinant Antibody (N192/12)
Anti-Gs protein, alpha subunit Recombinant Antibody (N192/12)
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Overview
Catalog No.HY062013
Description
Anti-Gs protein, alpha subunit Recombinant Antibody (N192/12) (HY062013) is a mouse monoclonal antibody detecting POLA1 in IHC, WB.
Highlights
  • ●Affinity Purified — Minimal background and high purity for reliable results.
  • ●Multi-Application — Validated across multiple applications.
ApplicationsIHC, WB
Host speciesMouse
ClonalityMonoclonal
IsotypeIgG2a, kappa
Clone IDN192/12
Target POLA1, POLA, DNA polymerase alpha catalytic subunit p180, DNA polymerase alpha catalytic subunit
Endotoxin level Please contact with the lab for this information.
Purity >95% as determined by SDS-PAGE.
Purification Protein A/G purified from cell culture supernatant.
RRID

Anti-Gs protein, alpha subunit Antibody (N192/12) (abinScience Cat# HY062013, RRID:AB_3728108)
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Form Liquid
Storage buffer 0.01M PBS pH 7.4

Please refer to the specific buffer information in the hardcopy of datasheet or the lot-specific COA.

Product Usage Information
Application Dilution
WB 1:500-1:2000
Stability and Storage Use a manual defrost freezer and avoid repeated freeze-thaw cycles. Store at 4°C short term (1-2 weeks). Store at -20°C 12 months. Store at -80°C long term.
Background

DNA polymerase alpha catalytic subunit (POLA1) is a ~165 kDa protein. Catalytic subunit of the DNA polymerase alpha complex (also known as the alpha DNA polymerase-primase complex) which plays 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, a regulatory subunit POLA2 and two primase subunits PRIM1 and 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. 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.

1. Starokadomskyy, P. et al. (2016) Nature immunology 17, 495-504. PMID: 27019227
Note For research use only.
Images
  • Anti-Gs protein, alpha subunit Recombinant Antibody (N192/12)

    SDS-PAGE

    SDS-PAGE for Anti-Gs protein, alpha subunit Antibody (N192/12)

References
Formula
Mass (g) = Concentration (mol/L) × Volume (L) × MW (g/mol)
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Formula
C₁ × V₁ = C₂ × V₂
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Stock Solution
C₁ (Stock Conc.)
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V₁ (Stock Vol.)
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Working Solution
C₂ (Working Conc.)
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