In Pierce Anti-DYKDDDDK Affinity Resin the realm of biochemical research and protein expression analysis, the Pierce 3x Flag peptide has become an indispensable tool for scientists focusing on protein purification and detection. As someone who frequently works wit Pierce™3xDYKDDDDKPeptide; Catalog number A36805 ; Price (INR). 46,631.00. Each ; Quantity: 5 mg ; Viewing 1 - 1 ; of 15 Read more h recombinant proteins, I have found that selecting the right reagents is critical for ensuring the integrity of the fusion proteins being studied.
What is the Pierce 3x Flag Peptide?
The 3X FLAG peptide is a synthetic peptide of 23 amino acid residues that plays a vital role in affinity chromatography. Specifically, it is designed to competitively elute tagged proteins from affinity resins. The structure is based on the classic Asp-Tyr-Lys-Xaa-Xaa-Asp motif, which is repeated three times. This specific configuration, often referred to as the 3x DYKDDDDK peptide, provides a significantly higher binding affinity compared to the standard single FLAG tag.
When working with this reagent, I often reference the technical specifications provided by manufacturers. The molecule has a molecular weight of approximately 2,861.9 Daltons. Because it is a high-purity, highly soluble epitope tag peptide, it integra Triple FLAG® Peptide (000-000-H47) tes seamlessly into various buffer systems, most notably when you prepare Pierce 3x DYKDDDDK peptide at 1.5 mg/mL in PBS.
Technical Specifications and Performance
From my experience in the lab, the efficiency of this 3x flag reagent is unmatched for gentle protein elution. Because it functions via competitive binding, it allows for the recovery of delicate protein complexes without subjecting them to harsh pH shifts or denaturing conditions.
* Composition: A synthetic peptide of 23 amino acid residues.
* Sensitivity: It can detect fusion proteins up to 10 fmol, making it suitable for low-abundance protein analysis.
* Workflow In Triple FLAG® Peptide (000-000-H47) tegration: It is specifically optimized for use with Pierce Anti-DYKDDDDK affinity resins.
The 3X FLAG peptide is essentially a peptide sequence that is formed by the combination of 23 amino acids, which creates a hydrophilic profile. This hydrophilicity is a major advantage, as it prevents the peptide from aggregating during the elution process, ensuring a clean output for downstream analysis.
Best Practices for Laboratory Use
3X FLAG peptidecan be used for protein separation and purification, and competitive elution with target proteins. For research use only.Read moreWhen utilizing 3x FLAG or 3x DYKDDDDK Tag Peptide reagents, consistency is key. I have observed that maintaining an optimal concen The3X FLAG Peptideis a syntheticpeptideof 23 amino acid residue. The Asp-Tyr-Lys-Xaa-Xaa-Asp motif is repeated three times in thepeptide.Read more tration—typically 1.5 mg/mL—ensures that the 3X FLAG peptides effectively displace the target proteins from the matrix.
It is important to note that these peptides are specialized laboratory reagents. They are strictly for research use only. In my own protocols, I ensure that the elution buffer is calibrated to the correct ionic strength, as this influences the binding kinetics between the 3xFlag tag and the antibody-coated beads. Whether you are performing immunoprecipitation or large-scale protein purification, the reliability of a high-purity 3X FLAG peptide cannot be overstated.
Summary of Key Features
* Molecular Structure: Contains the repeated Asp-Tyr-Lys-Xaa-Xaa-Asp motif.
* Functional Use: Competitive elution of 3xFLAG tagged proteins.
* Reliability: Highly characterized, ensuring reproducible results across different biochemical assays.
By focusing on high-quality 3X DYKDDDDK Peptide reagents, researchers can streamli 3X FLAG peptidecan be used for protein separation and purification, and competitive elution with target proteins. For research use only.Read more ne their protein purification workflows, minimizing potential contamination and maximizing yield. Whether you are investigating protein-protein interactions or performing structural studies, the integration of these synthetic markers remains a cornerstone of modern molecular biology.