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POLG Antibody

Rabbit Polyclonal Antibody

     
  • IF - POLG Antibody ALS13141
    Immunofluorescence of methanol-fixed HeLa, using DNA polymerase gamma antibody at 1:200 dilution.
    detail
  • WB - POLG Antibody ALS13141
    Sample (30 ug of whole cell lysate). A: 293T. 5% SDS PAGE. POLG antibody diluted at 1:5000.
    detail
  • IHC - POLG Antibody ALS13141
    Anti-POLG antibody IHC of human skeletal muscle.
    detail
  • SPECIFICATION
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  • BACKGROUND
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Product Information
Application
  • Applications Legend:
  • WB=Western Blot
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin-embedded Sections)
  • IHC-F=Immunohistochemistry (Frozen Sections)
  • IF=Immunofluorescence
  • FC=Flow Cytopmetry
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • E=ELISA
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
WB, IHC-P, IF, ICC
Primary Accession P54098
Reactivity Human
Host Rabbit
Clonality Polyclonal
Calculated MW 140kDa
Dilution ICC (1:100-1:200), IF (1:100-1:200), IHC-P (10 µg/ml), WB (1:1000-1:10000) ,
Additional Information
Gene ID 5428
Other Names DNA polymerase subunit gamma-1, 2.7.7.7, Mitochondrial DNA polymerase catalytic subunit, PolG-alpha, POLG, MDP1, POLG1, POLGA
Target/Specificity Human DNA polymerase gamma. Predicted cross-reactivity based on amino acid sequence homology: mouse (91%), rat (91%).
Reconstitution & Storage Aliquot and store at -20°C. Minimize freezing and thawing.
PrecautionsPOLG Antibody is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Name POLG {ECO:0000303|PubMed:10827171, ECO:0000312|HGNC:HGNC:9179}
Function Catalytic subunit of DNA polymerase gamma solely responsible for replication of mitochondrial DNA (mtDNA). Replicates both heavy and light strands of the circular mtDNA genome using a single-stranded DNA template, RNA primers and the four deoxyribonucleoside triphosphates as substrates (PubMed:9558343, PubMed:11477093, PubMed:19837034, PubMed:11897778, PubMed:15917273). Has 5' -> 3' polymerase activity. Functionally interacts with TWNK and SSBP1 at the replication fork to form a highly processive replisome, where TWNK unwinds the double- stranded DNA template prior to replication and SSBP1 covers the parental heavy strand to enable continuous replication of the entire mitochondrial genome. A single nucleotide incorporation cycle includes binding of the incoming nucleotide at the insertion site, a phosphodiester bond formation reaction that extends the 3'-end of the primer DNA, and translocation of the primer terminus to the post- insertion site. After completing replication of a mtDNA strand, mediates 3' -> 5' exonucleolytic degradation at the nick to enable proper ligation (PubMed:9558343, PubMed:11477093, PubMed:15167897, PubMed:26095671, PubMed:19837034, PubMed:11897778, PubMed:15917273). Highly accurate due to high nucleotide selectivity and 3' -> 5' exonucleolytic proofreading. Proficiently corrects base substitutions, single-base additions and deletions in non-repetitive sequences and short repeats, but displays lower proofreading activity when replicating longer homopolymeric stretches. Exerts exonuclease activity toward single-stranded DNA and double-stranded DNA containing 3'- terminal mispairs. When a misincorporation occurs, transitions from replication to a pro-nucleolytic editing mode and removes the missincorporated nucleoside in the exonuclease active site. Proceeds via an SN2 nucleolytic mechanism in which Asp-198 catalyzes phosphodiester bond hydrolysis and Glu-200 stabilizes the leaving group. As a result the primer strand becomes one nucleotide shorter and is positioned in the post-insertion site, ready to resume DNA synthesis (PubMed:10827171, PubMed:11477094, PubMed:11504725, PubMed:37202477). Exerts 5'-deoxyribose phosphate (dRP) lyase activity and mediates repair-associated mtDNA synthesis (gap filling) in base-excision repair pathway. Catalyzes the release of the 5'-terminal 2-deoxyribose-5- phosphate sugar moiety from incised apurinic/apyrimidinic (AP) sites to produce a substrate for DNA ligase. The dRP lyase reaction does not require divalent metal ions and likely proceeds via a Schiff base intermediate in a beta-elimination reaction mechanism (PubMed:9770471).
Cellular Location Mitochondrion. Mitochondrion matrix, mitochondrion nucleoid
Volume 50 µl
Research Areas
Citations (0)
citation

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Background

Involved in the replication of mitochondrial DNA. Associates with mitochondrial DNA.

References

Ropp P.A.,et al.Genomics 36:449-458(1996).
Lecrenier N.L.,et al.Gene 185:147-152(1997).
Watanabe T.K.,et al.Submitted (MAR-1996) to the EMBL/GenBank/DDBJ databases.
Bogenhagen D.F.,et al.J. Biol. Chem. 283:3665-3675(2008).
Van Goethem G.,et al.Nat. Genet. 28:211-212(2001).

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$ 467.50
Cat# ALS13141
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