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AB61241

Anti-p53 (acetyl K381) antibody

3

(1 Review)

|

(40 Publications )

Rabbit Polyclonal P53 acetyl K381 antibody. Suitable for IHC-P, ICC/IF and reacts with Human samples. Cited in 40 publications. Immunogen corresponding to Synthetic Peptide within Human TP53 acetyl K381.

View Alternative Names

P53, TP53, Cellular tumor antigen p53, Antigen NY-CO-13, Phosphoprotein p53, Tumor suppressor p53

2 Images
Immunocytochemistry/ Immunofluorescence - Anti-p53 (acetyl K381) antibody (AB61241)
  • ICC/IF

Unknown

Immunocytochemistry/ Immunofluorescence - Anti-p53 (acetyl K381) antibody (AB61241)

Immunofluorescence analysis of HeLa cells, using p53 (acetyl K381) antibody (ab61241) at 1/500 dilution, in the presence (right panel) or absence (left panel) of acetylated peptide (blocking peptide).

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-p53 (acetyl K381) antibody (AB61241)
  • IHC-P

Unknown

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-p53 (acetyl K381) antibody (AB61241)

Immunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue using p53 (acetyl K381) antibody (ab61241) at 1/50 dilution, in the presence (right panel) or absence (left panel) of acetylated peptide (blocking peptide).

Key facts

Host species

Rabbit

Clonality

Polyclonal

Isotype

IgG

Carrier free

No

Reacts with

Human

Applications

IHC-P, ICC/IF

applications

Immunogen

Synthetic Peptide within Human TP53 acetyl K381. The exact immunogen used to generate this antibody is proprietary information.

P04637

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Species", "Dilution Info", "Notes"], "tabs": { "all-applications": {"fullname" : "All Applications", "shortname": "All Applications"}, "IHCP" : {"fullname" : "Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)", "shortname":"IHC-P"}, "ICCIF" : {"fullname" : "Immunocytochemistry/ Immunofluorescence", "shortname":"ICC/IF"} }, "product-promise": { "all": "all", "testedAndGuaranteed": "tested", "guaranteed": "expected", "predicted": "predicted", "notRecommended": "not-recommended" } }, "values": { "Human": { "IHCP-species-checked": "testedAndGuaranteed", "IHCP-species-dilution-info": "1/50 - 1/100", "IHCP-species-notes": "<p></p>", "ICCIF-species-checked": "testedAndGuaranteed", "ICCIF-species-dilution-info": "1/100 - 1/500", "ICCIF-species-notes": "<p></p>" } } }

Properties and storage information

Form
Liquid
Purification technique
Affinity purification Protein A
Purification notes
Purified from rabbit antiserum by affinity chromatography using epitope specific acetylated peptide. The antibody against non acetylated peptide was removed by chromatography using non acetylated peptide corresponding to the acetylation site.
Storage buffer
pH: 7.4 Preservative: 0.02% Sodium azide Constituents: Sodium chloride, PBS, 50% Glycerol (glycerin, glycerine)
Shipped at conditions
Blue Ice
Appropriate short-term storage duration
1-2 weeks
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

The protein p53 also known as TP53 or tumor protein p53 has a molecular weight of approximately 53 kDa. It acts as a transcription factor and plays a major role in cell cycle regulation apoptosis and maintaining genomic stability. This protein mainly expresses in the nucleus of cells and acts as a critical regulator of cellular responses to stress signals including DNA damage. Scientists commonly use p53 antibodies in various assays like western blot and p53 immunofluorescence to detect and study its expression and functional status in cells.
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.

P53 mutation or inactivation is often associated with the development of cancer given its role in controlling cell division and preventing tumor formation. Specifically its dysfunction has been linked to cancers such as breast cancer and lung cancer. Additionally p53 can interact with other mutant proteins like Ras compounding mutations that contribute to tumor progression and aggressive cancer phenotypes. Understanding these interactions and the status of p53 can be important in developing targeted cancer therapies.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

Multifunctional transcription factor that induces cell cycle arrest, DNA repair or apoptosis upon binding to its target DNA sequence (PubMed : 11025664, PubMed : 12524540, PubMed : 12810724, PubMed : 15186775, PubMed : 15340061, PubMed : 17317671, PubMed : 17349958, PubMed : 19556538, PubMed : 20673990, PubMed : 20959462, PubMed : 22726440, PubMed : 24051492, PubMed : 24652652, PubMed : 35618207, PubMed : 36634798, PubMed : 38653238, PubMed : 9840937). Acts as a tumor suppressor in many tumor types; induces growth arrest or apoptosis depending on the physiological circumstances and cell type (PubMed : 11025664, PubMed : 12524540, PubMed : 12810724, PubMed : 15186775, PubMed : 15340061, PubMed : 17189187, PubMed : 17317671, PubMed : 17349958, PubMed : 19556538, PubMed : 20673990, PubMed : 20959462, PubMed : 22726440, PubMed : 24051492, PubMed : 24652652, PubMed : 38653238, PubMed : 9840937). Negatively regulates cell division by controlling expression of a set of genes required for this process (PubMed : 11025664, PubMed : 12524540, PubMed : 12810724, PubMed : 15186775, PubMed : 15340061, PubMed : 17317671, PubMed : 17349958, PubMed : 19556538, PubMed : 20673990, PubMed : 20959462, PubMed : 22726440, PubMed : 24051492, PubMed : 24652652, PubMed : 9840937). One of the activated genes is an inhibitor of cyclin-dependent kinases. Apoptosis induction seems to be mediated either by stimulation of BAX and FAS antigen expression, or by repression of Bcl-2 expression (PubMed : 12524540, PubMed : 17189187). Its pro-apoptotic activity is activated via its interaction with PPP1R13B/ASPP1 or TP53BP2/ASPP2 (PubMed : 12524540). However, this activity is inhibited when the interaction with PPP1R13B/ASPP1 or TP53BP2/ASPP2 is displaced by PPP1R13L/iASPP (PubMed : 12524540). In cooperation with mitochondrial PPIF is involved in activating oxidative stress-induced necrosis; the function is largely independent of transcription. Induces the transcription of long intergenic non-coding RNA p21 (lincRNA-p21) and lincRNA-Mkln1. LincRNA-p21 participates in TP53-dependent transcriptional repression leading to apoptosis and seems to have an effect on cell-cycle regulation. Implicated in Notch signaling cross-over. Prevents CDK7 kinase activity when associated to CAK complex in response to DNA damage, thus stopping cell cycle progression. Isoform 2 enhances the transactivation activity of isoform 1 from some but not all TP53-inducible promoters. Isoform 4 suppresses transactivation activity and impairs growth suppression mediated by isoform 1. Isoform 7 inhibits isoform 1-mediated apoptosis. Regulates the circadian clock by repressing CLOCK-BMAL1-mediated transcriptional activation of PER2 (PubMed : 24051492).
See full target information TP53 acetyl K381

Publications (40)

Recent publications for all applications. Explore the full list and refine your search

Journal of orthopaedic surgery and research 20:781 PubMed40835957

2025

Expression characteristics of miR-502-5p/p53/NF-κB signaling pathway in patients with different degrees of knee osteoarthritis: a cross-sectional observational study with methodological limitations.

Applications

Unspecified application

Species

Unspecified reactive species

Xiaozhe Zhang,Kesong Shi,Anmin Ruan,Pu Chen,Tao Zhang,Qingpu Wang

Science advances 10:eadp2229 PubMed39454005

2024

Temporal regulation of gene expression through integration of p53 dynamics and modifications.

Applications

Unspecified application

Species

Unspecified reactive species

Dan Lu,Marjan Faizi,Bryon Drown,Alina Simerzin,Joshua François,Gary Bradshaw,Neil Kelleher,Ashwini Jambhekar,Jeremy Gunawardena,Galit Lahav

The ocular surface 33:39-49 PubMed38679196

2024

HDAC1/2 and HDAC3 play distinct roles in controlling adult Meibomian gland homeostasis.

Applications

Unspecified application

Species

Unspecified reactive species

Xuming Zhu,Mingang Xu,Sarah E Millar

Nature communications 14:4820 PubMed37563109

2023

Hdac1 and Hdac2 regulate the quiescent state and survival of hair-follicle mesenchymal niche.

Applications

Unspecified application

Species

Unspecified reactive species

Hadas Sibony-Benyamini,Emil Aamar,David Enshell-Seijffers

RSC advances 12:3809-3827 PubMed35425455

2022

Design and synthesis of amino acid derivatives of substituted benzimidazoles and pyrazoles as Sirt1 inhibitors.

Applications

Unspecified application

Species

Unspecified reactive species

Nikil Purushotham,Mrityunjay Singh,Bugga Paramesha,Vasantha Kumar,Sharad Wakode,Sanjay K Banerjee,Boja Poojary,Shailendra Asthana

American journal of physiology. Lung cellular and molecular physiology 322:L449-L461 PubMed34984918

2022

The profibrotic and senescence phenotype of old lung fibroblasts is reversed or ameliorated by genetic and pharmacological manipulation of Slc7a11 expression.

Applications

Unspecified application

Species

Unspecified reactive species

Jeffrey D Ritzenthaler,Edilson Torres-Gonzalez,Yuxuan Zheng,Igor N Zelko,Victor van Berkel,David R Nunley,Biniam Kidane,Andrew J Halayko,Ross Summer,Walter H Watson,Jesse Roman

The Journal of investigative dermatology 142:77-87.e10 PubMed34284046

2021

HDAC1/2 Control Proliferation and Survival in Adult Epidermis and Pre‒Basal Cell Carcinoma through p16 and p53.

Applications

Unspecified application

Species

Unspecified reactive species

Xuming Zhu,Matthew Leboeuf,Fang Liu,Marina Grachtchouk,John T Seykora,Edward E Morrisey,Andrzej A Dlugosz,Sarah E Millar

Antioxidants (Basel, Switzerland) 10: PubMed33672392

2021

Signal Transducer and Activator of Transcription 3 (STAT3) Suppresses STAT1/Interferon Signaling Pathway and Inflammation in Senescent Preadipocytes.

Applications

Unspecified application

Species

Unspecified reactive species

Aisha Y Madani,Yasser Majeed,Houari B Abdesselem,Maha V Agha,Muneera Vakayil,Nour K Al Sukhun,Najeeb M Halabi,Pankaj Kumar,Shahina Hayat,Mohamed A Elrayess,Arash Rafii,Karsten Suhre,Nayef A Mazloum

Cell proliferation 54:e12991 PubMed33522656

2021

Sirtuin 1 ameliorates defenestration in hepatic sinusoidal endothelial cells during liver fibrosis via inhibiting stress-induced premature senescence.

Applications

Unspecified application

Species

Unspecified reactive species

Xiaoying Luo,Yangqiu Bai,Shuli He,Suofeng Sun,Xiaoke Jiang,Zhiyu Yang,Di Lu,Peiru Wei,Yuan Liang,Cong Peng,Yaru Wang,Ruli Sheng,Shuangyin Han,Xiuling Li,Bingyong Zhang

Scientific reports 10:12250 PubMed32704131

2020

Cardioprotective effects of miR-34a silencing in a rat model of doxorubicin toxicity.

Applications

Unspecified application

Species

Unspecified reactive species

Elena Piegari,Anna Cozzolino,Loreta Pia Ciuffreda,Donato Cappetta,Antonella De Angelis,Konrad Urbanek,Francesco Rossi,Liberato Berrino
View all publications

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