Product manual
Product use, preparation, operating conditions and storage.
A free-carboxylic-acid form for custom coupling after carboxyl activation or fluorescence-method development.
Packs & quoteA free carboxylic acid is not a preactivated NHS ester. Activate it using a sample-compatible method before coupling to an accessible primary amine; do not use it as an NHS reagent without activation.
For small molecules, peptides or amino-modified samples with a defined activation, coupling and purification procedure.
When comparing free dye and conjugate detection, match pH, solvent and concentration and consider environment-dependent spectral differences.
Use parameters for the exact catalog number when preparing reagents, setting reagent input or calculating results. Request a lot-specific CoA for test results.
Choose activator, solvent and pH for the actual carboxylic acid and target amine, then begin at small scale.
For targets containing multiple carboxyls and amines, assess self-crosslinking, site distribution and separation difficulty.
Record the 5- or 6-isomer and free-acid or NHS-ester form. Wavelengths differ among isomers and forms; retain the exact catalog number during lot comparisons, HPLC separation and probe transfer.
Choose an activation system compatible with this dye carboxylic acid and solvent. Record activator input, pH and time; do not add unactivated free acid to the sample as though it were an NHS ester.
React the activated dye with a sample carrying accessible primary amines. For samples with multiple carboxyl and amino groups, compare separate activation and excess-activator removal, monitoring self-crosslinking and recovery.
Select desalting, size-exclusion separation, dialysis or chromatography for the sample size. Remove free reagent before measuring concentration, labeling density and function. Residual free dye raises background and biases labeling-density calculations.
Use suitable chromatography, mass spectrometry or electrophoresis to distinguish conjugate, unreacted dye and by-products, then test probe function. Increased fluorescence or a color change alone does not establish covalent coupling.
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.
Omit the carboxyl activator, mix an equal amount of free dye with the sample and purify identically to assess adsorption and free-dye carryover.
Use an unlabeled aliquot from the same preparation to assess changes in function, aggregation and recovery.
Include free-dye or no-target-handle controls to distinguish conjugation from adsorption. Match exposure, gain or voltage during detection.
Use suitable HPLC, PAGE or mass spectrometry to assess probe purity and labeling, comparing function with the unlabeled sequence. Measure free dye and probe in the same buffer and pH so environmental changes are not mistaken for changes in labeling.
Include your sample, formulation and detection method when requesting application guidance.
Thermo Fisher Scientific · Carbodiimide crosslinker chemistry
Explains carboxyl activation, intermediate hydrolysis and self-crosslinking risks in multi-handle samples, informing free-acid dye activation and product analysis.
Not directly. The free acid needs activation; use this product’s molecular weight, solubility and input conditions.
A fluorescent free acid is used for analytical or coupling work; its fluorophore does not make it a specific nucleic-acid stain.
Remove free dye, characterize the product by suitable chromatography, mass spectrometry or electrophoresis, and check sample function.
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