Anti-SMUG1 antibody [EPR15624]
- RabMAb
- Recombinant
- KO Validated
- What is this?
5
(3 Reviews)
|
(10 Publications)
Rabbit Recombinant Monoclonal SMUG1 antibody. Suitable for IP, WB and reacts with Human samples. Cited in 10 publications.
View Alternative Names
Single-strand selective monofunctional uracil DNA glycosylase, SMUG1
- IP
Unknown
Immunoprecipitation - Anti-SMUG1 antibody [EPR15624] (AB192240)
Western blot analysis of immunoprecipitation pellet from 293 cell lysate immunoprecipitated using ab192240 at 1/100 dilution (lane 1) or PBS control (lane 2).
Secondary : Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG at 1/1500 dilution.
All lanes:
Immunoprecipitation - Anti-SMUG1 antibody [EPR15624] (ab192240)
Predicted band size: 29 kDa
false
- WB
Lab
Western blot - Anti-SMUG1 antibody [EPR15624] (AB192240)
Lanes 1 - 4 : Merged signal (red and green). Green - ab192240 observed at 30 kDa. Red - loading control ab7291 (Mouse anti-Alpha Tubulin [DM1A]) observed at 55kDa.
ab192240 was shown to react with SMUG1 in wild-type HAP1 cells in western blot with loss of signal observed in SMUG1 knockout sample. Wild-type and SMUG1 knockout HAP1 cell lysates were subjected to SDS-PAGE. Membranes were blocked in 3% milk in TBS-T (0.1% Tween®) before incubation with ab192240 and ab7291 (Mouse anti-Alpha Tubulin [DM1A]) overnight at 4°C at a 1 in 1000 Dilution and a 1 in 20000 dilution respectively. Blots were incubated with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed (ab216776) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-SMUG1 antibody [EPR15624] (ab192240) at 1/1000 dilution
Lane 1:
Wild-type HAP1 cell lysate at 20 µg
Lane 2:
SMUG1 knockout HAP1 cell lysate at 20 µg
Lane 3:
MOLT-4 cell lysate at 20 µg
Lane 4:
HEK-293 cell lysate at 20 µg
Predicted band size: 29 kDa
Observed band size: 30 kDa
false
- WB
Supplier Data
Western blot - Anti-SMUG1 antibody [EPR15624] (AB192240)
All lanes:
Western blot - Anti-SMUG1 antibody [EPR15624] (ab192240) at 1/5000 dilution
Lane 1:
MOLT4 cell lysate at 10 µg
Lane 2:
293 cell lysate at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugate at 1/1000 dilution
Predicted band size: 29 kDa
false
Related conjugates and formulations (2)
-
805 Alexa Fluor® 790
Donkey Anti-Rabbit IgG H&L (Alexa Fluor® 790) preadsorbed
-
Goat Anti-Rabbit IgG H&L (HRP)
Reactivity data
Product details
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
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.
Product protocols
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Target data
Publications (10)
Recent publications for all applications. Explore the full list and refine your search
Scientific reports 15:26617 PubMed40695981
2025
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Molecular cell 84:2036-2052.e7 PubMed38688279
2024
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International journal of biological sciences 20:1669-1687 PubMed38481813
2024
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Molecular cell 84:447-462.e10 PubMed38244544
2024
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Nucleic acids research 51:4881-4898 PubMed36971122
2023
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Frontiers in cardiovascular medicine 9:1053697 PubMed36620624
2022
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Nature 607:799-807 PubMed35859169
2022
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Nature 606:930-936 PubMed35477155
2022
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Molecular cell 81:767-783.e11 PubMed33333017
2020
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Cell reports 28:1690-1702.e10 PubMed31412240
2019
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Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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