• Western blot analysis of extracts of various cell lines, using DNA Polymerase gamma rabbit polyclonal antibody antibody (STJ110749) at 1:500 dilution. Secondary antibody: HRP Goat Anti-rabbit IgG (H+L) (STJS000856) at 1:10000 dilution. Lysates/proteins: 25 Mu g per lane. Blocking buffer: 3% non-fat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 60s.
  • Western blot analysis of extracts of mouse placenta, using DNA Polymerase gamma rabbit polyclonal antibody antibody (STJ110749) at 1:500 dilution. Secondary antibody: HRP Goat Anti-rabbit IgG (H+L) (STJS000856) at 1:10000 dilution. Lysates/proteins: 25 Mu g per lane. Blocking buffer: 3% non-fat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 180s.

Anti-POLG antibody (540-720) (STJ110749)

SKU:
STJ110749

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Host: Rabbit
Applications: WB/ELISA
Reactivity: Human/Mouse/Rat
Note: STRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.
Clonality: Polyclonal
Conjugation: Unconjugated
Isotype: IgG
Formulation: PBS with 0.05% Proclin300, 50% Glycerol, pH 7.3.
Purification: Affinity purification
Concentration: Lot specific
Dilution Range: WB:1:100-1:500
ELISA:Recommended starting concentration is 1 Mu g/mL. Please optimize the concentration based on your specific assay requirements.
Storage Instruction: Store at-20°C for up to 1 year from the date of receipt, and avoid repeat freeze-thaw cycles.
Gene Symbol: POLG
Gene ID: 5428
Uniprot ID: DPOG1_HUMAN
Immunogen Region: 540-720
Specificity: Recombinant fusion protein containing a sequence corresponding to amino acids 540-720 of human DNA Polymerase gamma (NP_002684.1).
Immunogen Sequence: QQDVMARACLQKLKGTTELL PKRPQHLPGHPGWYRKLCPR LDDPAWTPGPSLLSLQMRVT PKLMALTWDGFPLHYSERHG WGYLVPGRRDNLAKLPTGTT LESAGVVCPYRAIESLYRKH CLEQGKQQLMPQEAGLAEEF LLTDNSAIWQTVEELDYLEV EAEAKMENLRAAVPGQPLAL T
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. 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. 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. 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.
Protein Name Dna Polymerase Subunit Gamma-1
3'-5' Exodeoxyribonuclease
5'-Deoxyribose-Phosphate Lyase
Mitochondrial Dna Polymerase Catalytic Subunit
Polg-Alpha
Cellular Localisation Mitochondrion
Mitochondrion Matrix
Mitochondrion Nucleoid
Alternative Antibody Names Anti-Dna Polymerase Subunit Gamma-1 antibody
Anti-3'-5' Exodeoxyribonuclease antibody
Anti-5'-Deoxyribose-Phosphate Lyase antibody
Anti-Mitochondrial Dna Polymerase Catalytic Subunit antibody
Anti-Polg-Alpha antibody
Anti-POLG antibody
Anti-MDP1 antibody
Anti-POLG1 antibody
Anti-POLGA antibody

Information sourced from Uniprot.org

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