Goat Polyclonal SMUG1 antibody. Suitable for ICC, Flow Cyt (Intra) and reacts with Human samples. Cited in 2 publications. Immunogen corresponding to Synthetic Peptide within Human Single-strand selective monofunctional uracil DNA glycosylase aa 1-50.
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Single-strand selective monofunctional uracil DNA glycosylase, SMUG1
- ICC
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Immunocytochemistry - Anti-SMUG1 antibody (AB15716)
Immunocytochemistry/immunofluorescence analysis of MCF7 cells labelling SMUG1 with ab15716 at 10 μg/mL showing strong nuclear and cytoplasmic staining. Cells were fixed with paraformaldehyde and permeabilized with 0.15% Triton. Primary incubation for 1 hour. Alexa Fluor® 488 secondary antibody at 2 μg/mL (green). Nuclear DNA was labelled with DAPI (blue).
Negative control : Unimmunized goat IgG (10 μg/mL) followed by Alexa Fluor® 488 secondary antibody (2 μg/mL).
- ICC
Supplier Data
Immunocytochemistry - Anti-SMUG1 antibody (AB15716)
Immunocytochemistry/immunofluorescence analysis of U2OS cells labelling SMUG1 with ab15716 at 10 μg/mL showing strong nuclear staining. Cells were fixed with paraformaldehyde and permeabilized with 0.15% Triton. Primary incubation for 1 hour. Alexa Fluor® 488 secondary antibody at 2 μg/mL (green). Nuclear DNA was labelled with DAPI (blue).
Negative control : Unimmunized goat IgG (10 μg/mL) followed by Alexa Fluor® 488 secondary antibody (2 μg/mL).
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-SMUG1 antibody (AB15716)
Flow cytometric analysis of paraformaldehyde fixed MCF7 cells (blue line) labelling SMUG1 with ab15716. Cells permeabilized with 0.5% Triton. Primary incubation 1 hour (10 μg/mL) followed by Alexa Fluor® 488 secondary antibody (1 μg/mL). IgG control : Unimmunized goat IgG (black line) followed by Alexa Fluor® 488 secondary antibody.
Reactivity data
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Supplementary information
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Biological function summary
The process of DNA metabolism relies heavily on mechanisms related to the SMUG1 enzyme. As part of the DNA repair machinery it identifies and excises uracil bases from DNA which result from deamination of cytosine or misincorporation during DNA synthesis. SMUG1 does not function within a larger protein complex but interacts dynamically with other repair proteins like AP endonucleases. This activity helps maintain genomic stability by preventing mutations that could arise from uracil incorporation.
Pathways
SMUG1 contributes importantly to the base excision repair pathway an important process for DNA maintenance. This pathway addresses small non-helix-distorting base lesions such as deaminated oxidized or alkylated bases. Within this pathway SMUG1's activity aligns with other glycosylases and the APEX1 protein which processes the abasic sites left after SMUG1 removes uracil. Furthermore SMUG1's function supports the overall cellular DNA damage response signaling when repair and further processing are necessary.
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Publications (2)
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Nucleic acids research 42:1698-710 PubMed24178031
2013
Applications
Unspecified application
Species
Unspecified reactive species
FASEB journal : official publication of the Federa 25:4406-14 PubMed21891782
2011
Applications
WB
Species
Human
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