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Home Shop Biochemicals FOX04 DRI 10MG
Biochemicals Smart Peptide

FOX04 DRI 10MG

FOR RESEARCH SCIENTIFIC STUDIES ONLY- NOT FOR HUMAN/ANIMAL CONSUMPTION/USE

RESEARCH UNIT PRICE
$99.99
QUANTITY (VIALS)
In Stock
PURITY
99.2%
Pharmaceutical Grade
MOL. WEIGHT
1419.6 g/mol

Clinical Integrity

Every batch of Labrat Peptides undergoes third-party Mass Spectrometry and HPLC analysis. We believe in absolute transparency - since in third-party marketing we need complete confidence.

  • Third-party Laboratory Testing
  • Certified Endotoxin-Free
  • Vacuum Sealed Lyophilized Powder
Test TypeMass Spec / HPLC
Purity Result99.2%
AppearanceWhite Lyophilized Powder
CategoryCommercial
QualityPharmaceutical Grade

Research Application

FOXO4-DRI 10MG Research Peptide

FOXO4-DRI 10MG is a synthetic peptide research material investigated in laboratory studies involving cellular senescence, FOXO4-p53 signaling, apoptosis, aging biology, molecular interactions, and senescent-cell research.

FOXO4-DRI is a D-retro-inverso peptide designed to investigate the interaction between the FOXO4 protein and the tumor-suppressor protein p53. Experimental research has shown that the peptide can interfere with the FOXO4-p53 interaction, providing researchers with a molecular tool for studying mechanisms involved in the persistence and survival of senescent cells. PubMed Central (PMC)

Cellular senescence is a complex biological state characterized by stable changes in cell-cycle activity and cellular function. The FOXO4-p53 pathway has become an important subject of research because it may contribute to the survival of certain senescent cells.

The 10MG presentation provides a defined quantity of research material for appropriately designed laboratory experiments.

FOR RESEARCH USE ONLY. NOT FOR HUMAN OR VETERINARY USE.


What Is FOXO4-DRI?

FOXO4-DRI is a synthetic peptide developed to study the interaction between FOXO4 and p53.

FOXO4 belongs to the forkhead box O (FOXO) family of transcription factors. These proteins participate in numerous cellular processes, including:

  • Stress responses
  • Cellular metabolism
  • DNA damage responses
  • Cell-cycle regulation
  • Apoptosis
  • Cellular aging
  • Oxidative-stress signaling

FOXO4 has attracted particular interest in senescence research because of its interaction with p53.

Research has shown that FOXO4-DRI can compete with FOXO4 for interaction with p53, making the peptide useful as an experimental tool for investigating this protein-protein interaction. PubMed


FOXO4-p53 Research

The FOXO4-p53 axis is a major area of investigation in cellular senescence research.

p53 is a well-characterized tumor-suppressor protein involved in:

  • DNA damage responses
  • Cell-cycle regulation
  • Apoptosis
  • Cellular stress
  • Genomic stability

FOXO4 can interact with p53 under certain cellular conditions.

Experimental research has investigated whether disrupting this interaction can alter the survival characteristics of senescent cells.

Structural studies published in 2025 further characterized the interaction between FOXO4-DRI and the p53 transactivation domain, providing additional molecular information about how the peptide interacts with its target. PubMed


Cellular Senescence Research

Cellular senescence describes a stable cellular state associated with changes in proliferation, metabolism, gene expression, and secretory activity.

Senescent-cell research examines numerous biological markers, including:

  • p16
  • p21
  • p53
  • Senescence-associated β-galactosidase
  • DNA-damage markers
  • Senescence-associated secretory phenotype (SASP) factors
  • Cell-cycle changes

The accumulation of senescent cells is an active area of aging and cell-biology research.

FOXO4-DRI provides researchers with a tool for studying molecular mechanisms associated with senescent-cell survival and apoptosis.


Senolytic Peptide Research

A senolytic refers broadly to an experimental approach intended to selectively eliminate senescent cells.

FOXO4-DRI has been investigated as a senolytic peptide in preclinical research.

Earlier experimental work found that the peptide could interfere with FOXO4-p53 binding and promote apoptosis in senescent cells. PubMed Central (PMC)

This research has made FOXO4-DRI relevant to studies investigating:

  • Senescent-cell survival
  • Protein-protein interactions
  • Apoptosis
  • Cellular aging
  • Senescent-cell clearance
  • Molecular aging mechanisms

Importantly, these findings are primarily from experimental and preclinical models and should not be interpreted as established human therapeutic outcomes.


Apoptosis Research

Apoptosis is a regulated form of programmed cell death.

Researchers investigating apoptosis commonly measure:

  • Caspase activation
  • BAX expression
  • BCL-2 expression
  • Mitochondrial membrane changes
  • DNA fragmentation
  • Annexin V staining
  • Cellular morphology

Experimental research has reported that disrupting the FOXO4-p53 interaction can promote apoptosis in senescent cells under certain experimental conditions. PubMed

These observations provide opportunities for researchers to investigate the molecular relationship between senescence and programmed cell death.


p53 Signaling Research

p53 is one of the most extensively studied proteins in molecular biology.

It plays important roles in responding to cellular stress and DNA damage.

Researchers can examine:

  • p53 phosphorylation
  • p53 localization
  • p53 transcriptional activity
  • p53-dependent apoptosis
  • Protein-protein interactions
  • Cell-cycle regulation

Recent structural research found that FOXO4-DRI interacts with the p53 transactivation domain and provided additional information about the molecular basis of this interaction. PubMed


Nuclear Signaling Research

The location of signaling proteins within the cell can influence their function.

Research involving FOXO4 and p53 may therefore examine:

  • Nuclear localization
  • Cytoplasmic localization
  • Nuclear exclusion
  • Protein trafficking
  • Transcriptional activity

Experimental studies have reported that disruption of FOXO4-p53 interactions can influence p53 localization in senescent-cell models. PubMed Central (PMC)

Techniques such as immunofluorescence and cellular fractionation can be used to study these changes.


Aging Biology Research

Cellular aging is influenced by numerous interacting mechanisms.

Important research areas include:

  • Cellular senescence
  • Telomere biology
  • DNA damage
  • Mitochondrial function
  • Oxidative stress
  • Protein homeostasis
  • Autophagy
  • Epigenetic regulation
  • Inflammatory signaling

The FOXO4-p53 pathway represents one molecular mechanism being investigated within this broader field.

FOXO4-DRI can therefore be used as an experimental tool in studies examining relationships between protein interactions and cellular aging.


Oxidative Stress and FOXO4

FOXO transcription factors are closely associated with cellular stress responses.

Research into FOXO4 includes investigation of:

  • Reactive oxygen species
  • Redox signaling
  • Stress adaptation
  • Antioxidant pathways
  • Nuclear signaling
  • Cellular survival

A recent 2026 review examined FOXO4 as a redox-sensitive regulator and discussed the relationship between FOXO4, oxidative stress, cellular senescence, and p53 signaling. The review also emphasized that some proposed FOXO4 antioxidant functions remain incompletely established. PubMed

This distinction is important when interpreting experimental findings.


Endothelial Cell Research

Recent research has investigated FOXO4-DRI in models of endothelial-cell senescence.

A 2026 study reported that the peptide disrupted FOXO4-p53 interaction in experimental endothelial models and investigated downstream changes involving p53, BAX, BCL-2, and caspase-3. The study also used aged mouse models to investigate vascular effects. PubMed

These findings provide a current research direction for scientists studying:

  • Endothelial senescence
  • Vascular aging
  • p53 signaling
  • Apoptosis
  • Cellular stress

Because these observations come from experimental models, further research is required to determine their broader biological significance.


Fibroblast and Cellular Aging Research

FOXO4-DRI has also been investigated in experimental fibroblast models.

A 2025 study examining keloid-associated fibroblasts reported that the peptide promoted apoptosis in senescent fibroblast models and investigated changes involving phosphorylated p53 and nuclear localization. PubMed

This type of research can help scientists investigate whether the FOXO4-p53 interaction behaves differently across specific cell types and senescence models.


Cancer Biology Research

Cellular senescence is also relevant to cancer biology.

Senescent cancer cells and therapy-induced senescence are active areas of investigation because senescent cells can display altered signaling and secretory characteristics.

Researchers have investigated peptides targeting FOXO4-p53 interactions as experimental approaches for studying senescent cancer cells. PubMed

This does not establish FOXO4-DRI as a cancer treatment. Instead, it highlights its value as an experimental tool for investigating molecular mechanisms associated with senescent-cell survival.


Protein-Protein Interaction Research

One of the most interesting characteristics of this research peptide is its use in studying protein-protein interactions.

FOXO4-DRI research can investigate:

  • FOXO4-p53 binding
  • Competitive inhibition
  • Binding affinity
  • Structural interactions
  • Protein localization
  • Downstream signaling

Nuclear magnetic resonance (NMR) studies have provided structural information about FOXO4-DRI interaction with the p53 transactivation domain. PubMed

This makes the compound relevant to structural biology and molecular pharmacology research.


Molecular Biology Applications

Laboratories investigating this peptide may use several analytical approaches.

Western Blotting

Can be used to investigate proteins such as p53, FOXO4, BAX, BCL-2, and cleaved caspases.

Immunofluorescence

Can help visualize protein localization and nuclear/cytoplasmic distribution.

Co-Immunoprecipitation

Can be used to investigate protein-protein interactions.

RT-qPCR

Can measure changes in gene expression associated with senescence and apoptosis.

Flow Cytometry

Can assess cellular viability, apoptosis markers, and cell-cycle characteristics.

NMR Spectroscopy

Can provide structural information about peptide-protein interactions.


Senescence Markers

Researchers studying cellular senescence may evaluate several independent markers rather than relying on a single measurement.

Potential endpoints include:

  • p16 expression
  • p21 expression
  • p53 signaling
  • SA-β-gal activity
  • SASP-associated genes
  • DNA-damage markers
  • Cell-cycle arrest
  • Morphological changes

Using multiple markers can provide stronger evidence that cells have entered a senescent state.


Analytical Testing

Research peptides should be appropriately characterized before experimental use.

Potential analytical methods include:

  • HPLC
  • Reverse-phase HPLC
  • LC-MS
  • Mass spectrometry
  • Peptide mapping
  • Molecular-weight analysis

Testing may provide information about:

  • Identity
  • Purity
  • Molecular mass
  • Sample composition
  • Batch consistency

Researchers should review available batch-specific analytical documentation before beginning experiments.


Certificate of Analysis

A Certificate of Analysis (COA) can provide important batch-specific information.

Depending on the quality-control program, a COA may include:

  • Product identification
  • Lot number
  • Purity
  • Molecular weight
  • Analytical methodology
  • Testing date
  • Other applicable quality measurements

Maintaining batch records supports experimental traceability and reproducibility.

A COA describes analytical characteristics of a particular batch and should not be interpreted as evidence of human efficacy or safety.


Storage and Handling

Research peptides should be handled and stored according to the manufacturer's current product-specific documentation.

Potential factors affecting peptide integrity include:

  • Temperature
  • Moisture
  • Light
  • Container integrity
  • Storage duration
  • Environmental fluctuations

Laboratory personnel should minimize unnecessary exposure to conditions that may compromise sample integrity.


Laboratory Safety

This research material should be handled by appropriately trained laboratory personnel.

Standard laboratory practices may include:

  • Appropriate personal protective equipment
  • Clearly labeled containers
  • Controlled sample handling
  • Inventory documentation
  • Appropriate storage
  • Spill-management procedures
  • Proper laboratory waste disposal

Researchers should review the applicable SDS and product documentation before starting experimental work.


Research Applications

Potential areas of investigation include:

Cellular Senescence

Study of senescent-cell survival and molecular characteristics.

Senolytic Research

Investigation of experimental mechanisms for targeting senescent cells.

FOXO4-p53 Biology

Study of protein-protein interactions and signaling.

Apoptosis

Investigation of programmed cell death pathways.

Aging Biology

Research into cellular mechanisms associated with aging.

Molecular Pharmacology

Study of peptide-mediated protein interactions.

Structural Biology

Investigation of peptide-protein binding.

Cancer Biology

Research into senescence-associated mechanisms in cancer models.


Experimental Design Considerations

Researchers should consider:

Experimental Controls

Use appropriate negative and positive controls to distinguish specific effects from nonspecific cellular responses.

Cellular Model

Different cell types can have substantially different senescence pathways and responses.

Senescence Validation

Multiple senescence markers should ideally be used to validate the experimental model.

Protein Interaction Measurements

Co-immunoprecipitation, imaging, or structural techniques can provide complementary information.

Apoptosis Measurements

Multiple endpoints can help distinguish apoptosis from general cytotoxicity.

Replication

Independent experimental replicates improve reproducibility.


General Research Workflow

A laboratory study may follow:

Material Selection → Analytical Verification → Senescence Model → Experimental Exposure → Protein/Cellular Analysis → Apoptosis Assessment → Molecular Analysis → Data Interpretation

The precise workflow should be determined by the validated laboratory protocol and research objective.


Frequently Asked Questions

What is FOXO4-DRI?

FOXO4-DRI is a synthetic D-retro-inverso peptide designed to investigate the interaction between FOXO4 and p53.

What is the FOXO4-p53 axis?

It describes a molecular interaction between FOXO4 and the tumor-suppressor protein p53 that has been investigated in relation to senescent-cell survival.

What is a senolytic peptide?

A senolytic peptide is an experimental peptide investigated for its ability to preferentially affect senescent cells.

What research areas involve this peptide?

Research includes cellular senescence, apoptosis, aging biology, protein-protein interactions, p53 signaling, molecular biology, and experimental senolytic research.

How can its molecular interactions be studied?

Researchers may use techniques such as co-immunoprecipitation, NMR spectroscopy, Western blotting, and immunofluorescence.

Is FOXO4-DRI 10MG intended for human use?

No. This product is intended for research use only and is not intended for human or veterinary use.


Scientific & Educational Resources

For further scientific research, use authoritative resources such as:

PubMed – FOXO4-DRI Research

PubMed – FOXO4-p53 Research

PubMed – Cellular Senescence

PubMed – Senolytic Research

PubChem

National Center for Biotechnology Information

Recent peer-reviewed research provides useful information about the structural basis of the FOXO4-p53 interaction and ongoing experimental investigations of FOXO4-DRI. PubMed


Internal Links for LabRat Peptides

Use contextual internal links throughout the page.

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Researchers investigating related research peptides can explore the broader LabRat Peptides collection.

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Additional educational resources covering peptide science, cellular research, and laboratory methodologies are available through the LabRat Peptides Research Hub.

Relevant internal categories to link naturally where appropriate:

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Explore Related Research Materials

Researchers studying cellular aging, senescence, molecular signaling, and peptide research can explore the LabRat Peptides Research Collection.

For additional educational information covering peptide science, molecular biology, laboratory methodologies, and analytical testing, visit the LabRat Peptides Research Hub.


Research Disclaimer

FOR RESEARCH USE ONLY. NOT FOR HUMAN OR VETERINARY USE.

FOXO4-DRI 10MG is presented as research material for controlled scientific investigation. The information provided is intended for educational and research purposes only and does not constitute medical advice, treatment recommendations, dosing instructions, or instructions for human or veterinary administration.

Published findings concerning this peptide are primarily derived from experimental and preclinical research. Results observed in cell or animal models should not automatically be interpreted as evidence of human therapeutic efficacy or safety. Recent reviews specifically note that FOXO4-DRI remains preclinical and that additional pharmacokinetic, delivery, toxicology, and tissue-specific research is needed. PubMed

Researchers are responsible for complying with applicable laws, institutional requirements, laboratory safety procedures, manufacturer documentation, and approved research protocols.

Specifications

SequenceAvailable on COA
AppearanceWhite Lyophilized Powder
Mol. Weight1419.6 g/mol
Purity99.2%
Storage-20°C or below
© 2026 LabRat Peptides. For laboratory research use only.Not for human consumption
CAUTION: PRODUCTS ARE INTENDED FOR RESEARCH USE ONLY. THE USE OF THESE PRODUCTS IN ANY HUMAN OR ANIMAL CAPACITY IS STRICTLY PROHIBITED BY LAW.
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