Protein timeless homolog (848-856)

Protein timeless homolog

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.

CAT No: ta-059

Synonyms/Alias:Protein timeless homolog (848-856)

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cGMP Peptide
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  • IND and NDA support
  • Drug master files (DMF) filing
Sequence
AILAHLNTV
Areas of Interest
Antigen-presenting Cells; Cancer Research

Protein timeless homolog (848-856) is a synthetic peptide fragment derived from the C-terminal region of the mammalian TIMELESS protein, a key component in circadian rhythm regulation and DNA replication processes. As a defined sequence peptide, it serves as a valuable molecular tool for dissecting the functional domains and protein-protein interaction sites within the TIMELESS protein family. Researchers utilize such peptides to gain insights into the mechanistic underpinnings of cell cycle progression, DNA damage response, and the molecular machinery governing circadian oscillations in eukaryotic systems. The sequence specificity and biochemical relevance of this fragment make it a versatile reagent for a range of molecular and cellular biology investigations.

Peptide interaction studies: In protein biochemistry and molecular biology, the 848-856 fragment is commonly used to investigate the binding interfaces of TIMELESS with its interaction partners, such as components of the circadian clock or DNA replication complexes. By employing this peptide in binding assays or affinity purification experiments, researchers can map and characterize the critical residues involved in protein-protein interactions, thereby elucidating the structural determinants of complex formation. Such studies contribute to a deeper understanding of the regulatory networks that coordinate cellular timekeeping and genome stability.

Epitope mapping and antibody validation: The defined sequence of the 848-856 peptide allows it to function as a standard in epitope mapping experiments. Laboratories frequently use synthetic peptides corresponding to regions of larger proteins to validate antibody specificity or to generate custom antibodies against unique epitopes. By incorporating this fragment into immunoassays, scientists can confirm the selective recognition of TIMELESS by monoclonal or polyclonal antibodies, facilitating the development of robust analytical tools for protein detection and quantification in diverse sample types.

Functional assays in cell signaling: The peptide serves as a modulator or competitor in functional assays designed to probe the role of TIMELESS in signaling pathways. By introducing the 848-856 fragment into in vitro or cell-based systems, researchers can competitively inhibit native protein-protein interactions or assess the impact of this domain on downstream signaling events. These approaches are instrumental in delineating the contribution of specific TIMELESS motifs to cell cycle checkpoints, DNA repair mechanisms, or circadian rhythm regulation.

Peptide-based inhibitor design: The structural and sequence information provided by the 848-856 region is valuable for rational drug design and the development of peptide-based inhibitors targeting TIMELESS or its binding partners. Structure-activity relationship studies often utilize such fragments to identify minimal binding motifs or to engineer modified peptides with enhanced affinity or stability. These efforts support early-stage research in modulating protein function for applications in basic science and biotechnology.

Analytical standards and assay calibration: Synthetic peptides like the 848-856 fragment are routinely employed as quantitative standards or positive controls in mass spectrometry-based proteomics and other analytical platforms. Their defined composition and stability allow for accurate calibration of detection systems, validation of peptide identification workflows, and benchmarking of assay performance. This ensures reproducibility and reliability in high-throughput analyses of TIMELESS expression, post-translational modifications, or interaction networks across experimental models.

Source#
Homo sapiens (human)
Epitope
848-856
Restricting HLA
HLA-class I
References
Chopie Hassan; Mol Cell Proteomics 2013

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