Anti-p53 (acetyl K370) antibody [EPR17496]
- RabMAb
- Recombinant
- Lab Essentials
- 20ul selling size
- What is this?
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(1 Review)
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(40 Publications)
Rabbit Recombinant Monoclonal P53 acetyl K370 antibody. Suitable for IP, WB, ICC/IF, Flow Cyt (Intra) and reacts with Human, Mouse, Rat samples. Cited in 40 publications.
View Alternative Names
P53, TP53, Cellular tumor antigen p53, Antigen NY-CO-13, Phosphoprotein p53, Tumor suppressor p53
- IP
Supplier Data
Immunoprecipitation - Anti-p53 (acetyl K370) antibody [EPR17496] (AB183544)
p53 (acetyl K370) was immunoprecipitated from 1mg of HepG2 (Human liver hepatocellular carcinoma) whole cell extract treated with Etoposide 20uM and Trichostatin A 500 nM for 6 hours with ab183544 at 1/100 dilution. Western blot was performed from the immunoprecipitate using ab183544 at 1/1000 dilution. Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG, was used as secondary antibody at 1/1500 dilution. Lane 1 : HepG2 whole cell extract treated with Etoposide 20uM and Trichostatin A 500 nM for 6 hours. Lane 2 : PBS instead of HepG2
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
All lanes:
Immunoprecipitation - Anti-p53 (acetyl K370) antibody [EPR17496] (ab183544)
Predicted band size: 43 kDa
Observed band size: 53 kDa
false
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-p53 (acetyl K370) antibody [EPR17496] (AB183544)
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 NIH/3T3 (Mouse embyro fibroblast cells) cells labeling p53 (acetyl K370) with ab183544 at 1/500 dilution, followed by Goat anti-rabbit Alexa Fluor® 488 IgG) (ab150077) secondary antibody at 1/400 dilution (green). Confocal image showing nuclear and weakly cytoplasm staining on NIH/3T3 cell line.
The expression increased after treatment with Trichostatin A (500 ng/ml) for 4 hours. The nuclear counter stain is DAPI (blue). Tubulin is detected with ab7291 (anti-Tubulin mouse mAb) at 1/500 dilution and ab150120 (goat anti-mouse AlexaFluor®594 secondary antibody) at 1/500 dilution (red).
The negative controls are as follows;
1. ab183544 at 1/500 dilution followed by ab150120 (goat anti-mouse AlexaFluor®594 secondary antibody) at 1/500 dilution.
2. ab7291 (anti-Tubulin mouse mAb) at 1/500 dilution followed by ab150077 (goat anti-rabbit Alexa Fluor®488 (IgG H&L) at 1/400 dilution.
[J Cell Biol. May 22, 2006; 173(4) : 533–544.]
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-p53 (acetyl K370) antibody [EPR17496] (AB183544)
Intracellular Flow Cytometry analysis of NIH/3T3 (mouse embryo) treated (Red)/untreated (Green) with 500ng/ml Trichostatin A for 4 hours with purified ab183544 at 1/150 dilution. The secondary antibody was Goat anti rabbit IgG (Alexa Fluor® 488) at 1/2000 dilution. A Rabbit monoclonal IgG (Black) was used as the isotype control and cells without incubation with primary antibody and secondary antibody (Blue) were used as unlabeled control.
- WB
Supplier Data
Western blot - Anti-p53 (acetyl K370) antibody [EPR17496] (AB183544)
Blocking/Dilution buffer : 5% NFDM/TBST
All lanes:
Western blot - Anti-p53 (acetyl K370) antibody [EPR17496] (ab183544) at 1/1000 dilution
Lane 1:
HepG2 (human hepatocellular carcinoma) treated with Etoposide 20uM and Trichostatin A 500 nM for 6 hours whole cell lysates at 10 µg
Lane 2:
HepG2 (human hepatocellular carcinoma) untreated whole cell lysates at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L),Peroxidase conjugated at 1/1000 dilution
Predicted band size: 43 kDa
Observed band size: 53 kDa
false
- WB
Supplier Data
Western blot - Anti-p53 (acetyl K370) antibody [EPR17496] (AB183544)
Blocking/Dilution buffer : 5% NFDM/TBST
All lanes:
Western blot - Anti-p53 (acetyl K370) antibody [EPR17496] (ab183544) at 1/10000 dilution
Lane 1:
NIH/3T3 (mouse embryo) treated with Trichostatin A 500 nM for 4hr whole cell lysates at 10 µg
Lane 2:
NIH/3T3 (mouse embryo) untreated whole cell lysates at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L),Peroxidase conjugated at 1/1000 dilution
Predicted band size: 43 kDa
Observed band size: 53 kDa
false
- WB
Supplier Data
Western blot - Anti-p53 (acetyl K370) antibody [EPR17496] (AB183544)
Blocking/Dilution buffer : 5% NFDM/TBST
All lanes:
Western blot - Anti-p53 (acetyl K370) antibody [EPR17496] (ab183544) at 1/1000 dilution
Lane 1:
C6 (rat glioma) treated with Trichostatin A 500 nM for 4hr whole cell lysates at 10 µg
Lane 2:
C6 (rat glioma) untreated whole cell lysates at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L),Peroxidase conjugated at 1/1000 dilution
Predicted band size: 43 kDa,48 kDa
Observed band size: 46 kDa,53 kDa,54 kDa
false
Related conjugates and formulations (2)
-
Anti-p53 (acetyl K370) antibody [EPR17496] - BSA and Azide free
-
665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-p53 (acetyl K370) antibody [EPR17496]
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
P53 functions to control cell division and apoptosis serving as a guardian of the genome by preventing mutation accumulation. It does not form part of a larger complex under normal conditions but interacts with various other molecules to execute its functions. p53 can activate or suppress the transcription of numerous genes involved in cell cycle arrest DNA repair and programmed cell death allowing it to halt the progression of damaged cells and trigger repair mechanisms or eliminate those that cannot be repaired.
Pathways
P53 acts within several key biological pathways such as the p53 signaling pathway and the intrinsic apoptotic pathway. Its activity involves interaction with proteins like MDM2 which regulates p53 through ubiquitin-mediated degradation and ATM kinase which phosphorylates p53 in response to DNA damage. These interactions ensure appropriate cellular responses during stress and are vital for maintaining homeostasis.
Product protocols
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Target data
Publications (40)
Recent publications for all applications. Explore the full list and refine your search
Cell death & disease 15:826 PubMed39543094
2024
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Biomacromolecules 25:4215-4232 PubMed38845149
2024
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Journal of molecular and cellular cardiology 192:36-47 PubMed38734062
2024
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Journal of neuroinflammation 20:208 PubMed37697347
2023
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Nature communications 14:4820 PubMed37563109
2023
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Cell death discovery 9:12 PubMed36653338
2023
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Journal of cell science 135: PubMed36239052
2022
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Molecular medicine reports 26: PubMed36004485
2022
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Skeletal muscle 12:19 PubMed35906707
2022
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The journal of physiological sciences : JPS 72:15 PubMed35850611
2022
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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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