Cell Signaling Technology

Product Pathways - Cell Cycle / Checkpoint

p48 Primase (8G10) Rat mAb #4725

Applications Reactivity Sensitivity MW (kDa) Isotype
W H M R Mk Endogenous 48 Rat IgG1

Applications Key:  W=Western Blotting
Reactivity Key:  H=Human  M=Mouse  R=Rat  Mk=Monkey
Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

Protocols

Specificity / Sensitivity

p48 Primase (8G10) Rat mAb detects endogenous levels of total p48 primase protein.

Source / Purification

Monoclonal antibody is produced by immunizing animals with full-length recombinant human p48 primase.

Western Blotting

Western Blotting

Western blot analysis of extracts from various cell types using p48 Primase (8G10) Rat mAb.

Background

Initiation of eukaryotic DNA replication is a stringently regulated process that requires the cooperation of many proteins and protein complexes to occur efficiently, at the origins of replication, and once per cell cycle. The initiation of DNA replication requires a protein complex composed of two DNA polymerase α subunits and a pair of primase subunits. Primase activity catalyzes de novo synthesis of an RNA/DNA primer (initiator DNA) on the leading and lagging strands, while polymerase activity extends the initiator DNA (1). The 48 and 58 kDa primase subunits cooperate in the synthesis of small RNA primers. p48 is the catalytically active subunit (2), while p58 couples p48 to the polymerase to allow the transfer of primers to the active site. The p58 subunit may also play a role in regulation of primer length (3,4).

  1. Shiratori, A. et al. (1995) Genomics 28, 350-353.
  2. Copeland, W.C. (1997) Protein Expr. Purif. 9, 1-9.
  3. Copeland, W.C. and Wang, T.S. (1993) J. Biol. Chem. 268, 26179-26189.
  4. Arezi, B. and Kuchta, R.D. (2000) Trends Biochem. Sci. 25, 572-576.

Application References

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For Research Use Only. Not For Use In Diagnostic Procedures.

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