Rabbit Recombinant Monoclonal UNG antibody. Suitable for Dot, IHC-P, WB and reacts with Synthetic peptide, Human samples.
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
Dot | IHC-P | WB | |
---|---|---|---|
Human | Expected | Tested | Tested |
Mouse | Not recommended | Not recommended | Not recommended |
Synthetic peptide | Tested | Not recommended | Not recommended |
Species | Dilution info | Notes |
---|---|---|
Species Synthetic peptide | Dilution info 1/1000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/100 | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Synthetic peptide | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/1000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Synthetic peptide | Dilution info - | Notes - |
Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine.
DGU, UNG1, UNG15, UNG, Uracil-DNA glycosylase, UDG
Rabbit Recombinant Monoclonal UNG antibody. Suitable for Dot, IHC-P, WB and reacts with Synthetic peptide, Human samples.
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
The immunogen is located within the N-terminal region of UNG2 (P13051-1). Based on peptide dot blot data we do not expect this antibody to cross-react with UNG1 (P13051-2).
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:
For more information, read more on recombinant antibodies.
UNG2 also known as uracil-DNA glycosylase 2 is a DNA repair enzyme with a mass of about 36 kDa. It operates mainly in the cell nucleus where it plays an important role in the base excision repair pathway. The enzyme detects and removes uracil from DNA molecules which often forms through deamination of cytosine or incorporation of dUMP instead of dTMP during DNA replication. By cleaving the N-glycosidic bond of uracil UNG2 initiates a repair process that helps maintain genetic integrity.
The enzyme has a significant role in preserving the accuracy of genetic information. UNG2 works independently but it acts closely with other repair enzymes in the context of DNA damage response. UNG2 excises uracil efficiently facilitating downstream actions by other repair mechanisms which complete the repair process. The enzyme's activity ensures that DNA mutations which may compromise cellular functions or lead to diseases do not accumulate.
The enzyme participates actively in the base excision repair pathway. This pathway critical for correcting small base lesions in DNA involves several components including APE1 and DNA polymerase beta. UNG2 collaborates with these proteins to ensure successful repair. Beyond this UNG2's activity is also linked to immunoglobulin gene diversification processes necessary for adaptive immunity thereby involving itself in immunity pathways.
Excessive or deficient activity of UNG2 links to certain conditions. Disruption in UNG2 function may contribute to cancer development due to its role in repairing DNA and preventing mutations. The enzyme's actions also intersect with viral infections; certain viruses such as Epstein-Barr virus may manipulate UNG2 function to favor their replication. Exploring these interactions can provide insights into potential therapeutic targets for these conditions.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.
In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
UNG2 Dot Blot staining using rabbit Anti-UNG2 antibody
Dot blot analysis of UNG2 using ab318982 at 1:1000 (0.501 ug/ml) followed by a Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1:100,000 dilution.
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
Peptides are located within the N-terminal region of UNG1 (P13051-2) and UNG2 (P13051-1). This antibody does not cross-react with human UNG1.
All lanes: Dot Blot - Anti-UNG2 antibody [EPR29004-78] (ab318982) at 1/1000 dilution
Lane 1: UNG2 peptide
Lane 2: UNG1 peptide
All lanes: Dot Blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/100000 dilution
Exposure time: 180s
UNG2 Western blot staining using rabbit Anti-UNG2 antibody
In Western blot, Anti-Vinculin antibody [EPR8185] (Anti-Vinculin antibody [EPR8185] - Loading Control ab129002) staining at 1/10000 dilution.
All lanes: Western blot - Anti-UNG2 antibody [EPR29004-78] (ab318982) at 1/1000 dilution
Lane 1: HeLa (human cervical adenocarcinoma epithelial cell) transfected with scrambled siRNA control whole cell lysate at 50 µg with NFDM/TBST
Lane 2: HeLa transfected with siRNA specifically targeting UNG2 whole cell lysate at 50 µg with NFDM/TBST
Lane 3: 293T (human embryonic kidney epithelial cell) whole cell lysate at 50 µg with NFDM/TBST
Lane 4: Caco-2 (human colorectal adenocarcinoma epithelial cell) whole cell lysate at 50 µg with NFDM/TBST
Lane 5: T-47D (human ductal breast epithelial tumor epithelial cell) whole cell lysate at 50 µg with NFDM/TBST
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/100000 dilution
Observed band size: 37 kDa, 124 kDa
Exposure time: 180s
Immunohistochemical analysis of paraffin-embedded Human smooth muscle tissue labeling UNG2 with ab318982 at 1/100 (5.33 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control: No staining in human smooth muscle.
The section was incubated with ab318982 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
Immunohistochemical analysis of paraffin-embedded Human lung cancer tissue labeling UNG2 with ab318982 at 1/100 (5.33 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining in human lung cancer.
The section was incubated with ab318982 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
Immunohistochemical analysis of paraffin-embedded Human colon tissue labeling UNG2 with ab318982 at 1/100 (5.33 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining in human colon.
The section was incubated with ab318982 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
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