Product manual
Product use, preparation, operating conditions and storage.
A fluorescent-protein donor and dye acceptor tandem for developing conjugates matched to the intended detection channel.
Packs & quoteAfter donor excitation, energy is transferred to the acceptor. Light, fixation and storage can alter this relationship, changing acceptor signal and donor leakage. Compensation or unmixing references should match reagent lot and processing.
After preparing the target conjugate, assess binding, free fluorescent-protein carryover and aggregation.
Configure the detection channel from this reagent’s optical properties, lasers and filters, then establish single-stain references.
Use parameters for the exact catalog number when preparing reagents, setting reagent input or calculating results. Request a lot-specific CoA for test results.
Use an appropriate aqueous buffer for the formulation, avoiding organic solvents, harsh mixing and unsuitable freeze–thaw cycles.
Check existing sites and any linker handles to be introduced. Do not use a fluorescent-protein reagent as though it were a small-molecule NHS dye.
Confirm by catalog number whether an activated handle is supplied and plan matching handles on the fluorescent material and target. Follow the supplied group for preactivated products, avoiding reactivation; remove free activator or reductant from each processed component.
This product uses a PE donor system. Check donor excitation, acceptor emission and acquisition windows by catalog number. The acceptor name does not specify donor excitation; monitor both acceptor signal and donor leakage in single stains.
Check concentration, buffer and optical properties, including visible precipitation and aggregation.
Use a validated activation and coupling procedure, titrating inputs and recording recovery and reaction conditions.
Both the fluorescent material and target antibody are macromolecules. Ordinary desalting or ultrafiltration does not ensure separation of the final conjugate from free fluorescent protein. Validate the resolving power of size-exclusion or another method, then assess recovery, purity and function.
Compare initial and stored acceptor signal and donor-channel leakage, using lot- and processing-matched single stains for compensation or unmixing.
Select a document and enter your phone and email. Include the lot number for a CoA.
Product use, preparation, operating conditions and storage.
Spectra, measurement conditions and detection settings for the exact catalog number.
Lot-specific test results. Include the lot number from the vial.
Handling, storage and emergency response information.
Compare free protein and the target conjugate to assess nonspecific adsorption.
Use matching references for each lot and fixation treatment rather than automatically substituting another same-name lot.
Use an unlabeled aliquot from the same preparation to assess changes in function, aggregation and recovery.
R&D Systems · Tandem Dye-Conjugated Antibodies FAQs
The source concerns conjugated antibodies and informs energy transfer, degradation and lot-matched controls. Qihe’s tandem series contains labeling reagents; validate the final conjugate with lot- and process-matched single stains. The source is not a raw-reagent conjugation recipe.
Cossarizza A, Chang HD, Radbruch A, et al. · European Journal of Immunology · 51(12):2708–3145 · 2021
Provides methodological guidance on detection settings, controls and experimental records for downstream conjugate evaluation.
It is a fluorescent-protein or tandem reagent. Specific recognition requires a suitable antibody or targeting molecule.
Fluorescent proteins require structural preservation. Follow the aqueous formulation rather than small reactive-dye stock methods.
Tandems can be affected by fixation and storage. Compare acceptor and donor channels through the complete process and verify single-stain references.
First identify the supplied reactive group, then prepare a matching target handle. Reactivation can change handle density and protein condition; the reagent name alone does not establish activation.
Acceptor composition, processing and storage can affect tandem spectra. Use the actual conjugate with lot- and processing-matched references for compensation or unmixing, and recheck after fixation or storage changes.
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