Anti-NUDT9 antibody [EPR15175]
- RabMAb
- Recombinant
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(1 Publication)
Rabbit Recombinant Monoclonal NUDT9 antibody. Suitable for WB, ICC/IF, Flow Cyt (Intra), IHC-P and reacts with Human, Rat samples. Cited in 1 publication.
View Alternative Names
NUDT10, PSEC0099, UNQ3012/PRO9771, NUDT9, ADP-ribose diphosphatase, ADP-ribose phosphohydrolase, Adenosine diphosphoribose pyrophosphatase, Nucleoside diphosphate-linked moiety X motif 9, ADPR-PPase, Nudix motif 9
- WB
Supplier Data
Western blot - Anti-NUDT9 antibody [EPR15175] (AB197021)
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-NUDT9 antibody [EPR15175] (ab197021) at 1/20000 dilution
Lane 1:
Jurkat (Human T cell leukemia cells from peripheral blood) cell lysate at 20 µg
Lane 2:
HUVEC (Human umbilical vein endothelial cell line) cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 39 kDa
Observed band size: 39 kDa
false
Exposure time: 30s
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-NUDT9 antibody [EPR15175] (AB197021)
Immunohistochemical analysis of paraffin-embedded Human kidney tissue labeling NUDT9 with ab197021 at 1/500 dilution followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution. Cytoplasm staining on Human kidney tissue is observed. Counter stained with Hematoxylin.
Negative control : Used PBS instead of primary antibody secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-NUDT9 antibody [EPR15175] (AB197021)
Immunohistochemical analysis of paraffin-embedded Rat kidney tissue labeling NUDT9 with ab197021 at 1/500 dilution followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution. Cytoplasm staining on Rat kidney tissue is observed. Counter stained with Hematoxylin.
Negative control : Used PBS instead of primary antibody secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-NUDT9 antibody [EPR15175] (AB197021)
Immunofluorescent analysis of 4% paraformaldehyde-fixed 0.1% Triton X-100 permeabilized HeLa (Human epithelial cells from cervix adenocarcinoma) cells labeling NUDT9 with ab197021 at 1/250 dilution followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/500 dilution (green). Mitochondrion staining on HeLa cell line is observed. The nuclear counterstain is DAPI (blue). COX IV is detected with ab33985 (anti-COX IV mouse mAb) at 1/1000 dilution and ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution (red).
The negative controls are as follows : -
-ve control 1 : ab197021 at 1/250 dilution followed by ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution.
-ve control 2 : ab33985 (anti-COX IV mouse mAb) at 1/1000 dilution followed by ab150077 (Alexa Fluor®488 Goat Anti-Rabbit IgG H&L) at 1/500 dilution.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-NUDT9 antibody [EPR15175] (AB197021)
Intracellular flow cytometric analysis of 2% paraformaldehyde-fixed Jurkat (Human T cell leukemia cells from peripheral blood) cells labeling NUDT9 with ab197021 at 1/170 dilution (red) compared with a rabbit monoclonal IgG isotype control (black) and an unlabelled control (cells without incubation with primary antibody and secondary antibody; blue). Goat anti rabbit IgG (FITC) at 1/150 dilution was used as the secondary antibody.
Reactivity data
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Properties and storage information
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Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
NUDT9 helps to maintain cellular balance by controlling levels of ADP-ribose a substrate for poly ADP-ribose polymerases. This regulation is essential for energy metabolism and DNA repair processes. NUDT9 operates independently and does not blend into larger protein complexes focusing strictly on its enzymatic role ensuring the cell's homeostasis.
Pathways
NUDT9 is significantly involved in NAD+ metabolism and the DNA repair mechanism. By converting ADP-ribose NUDT9 interacts with pathways that are central to maintaining cellular energy balance and protecting cells from DNA damage. It is functionally linked with enzymes such as PARP (poly ADP-ribose polymerase) which are pivotal in detecting and signaling DNA strand breaks.
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Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Cell death & disease 12:889 PubMed34588426
2021
Applications
Unspecified application
Species
Unspecified reactive species
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