The Lightning-Link conjugation kit allows fluorescent conjugations to be set up in seconds, simply by adding a solution of the protein to be labeled to the lyophilised mixture containing a proprietary activated fluorescent ligand.
By circumventing the desalting or dialysis steps that commonly interrupt traditional protein conjugation procedures, Lightning-Link technology can be used to label small quantities of protein with 100% recovery and no excessive dilution of the conjugate.
Upon dissolution of Lightning-Link mixture with a solution of the antibody (or other biomolecule to be labeled) proprietary chemicals in the mixture become activated. This results in coupling of the antibody to the fluorescent dye, in a gentle and controlled process at near-neutral pH. Lightning-Link makes it possible to conjugate primary antibodies and other proteins with ease, using a simple, efficient process that has safeguards to prevent over-labeling of the biomolecule and that ensures 100% recovery even at small scale.
- Considerations before use
- Sample buffer
Ideally, the antibody to be labeled should be in 10-50mM amine-free buffer pH range 6.5 to 8.5. However, many buffers outside these limits of concentration and pH can be accommodated. Modest concentrations of Tris buffer are also tolerated. Appendix 1 gives further guidance on buffers and compatible additives.
- Amount and volume of antibody
The recommended amount of antibody to be used for labeling is 100-200ug for 791-0010 and 1-2mg for 791-0015. The volume of the antibody sample, ideally, should be in the range 40-100ul (791-0010), and 400-1000ul (791-0015). Antibody concentrations of 1-4 mg/ml generally give optimal results, but concentrations and volumes outside the suggested ranges have also yielded excellent conjugates.
- Setting up conjugation reactions
- Before you add antibody to the Lightning-Link mix, add 1ul of LL-Modifier reagent for each 10ml of antibody to be labeled. Mix gently.
- Remove the screw cap from the vial of Lightning-Link mix and pipette the antibody sample (with added LL-modifier) directly onto the lyophilised material. Resuspend gently by withdrawing and re-dispensing the liquid once or twice using a pipette.
- Place the cap back on the vial and leave the vial standing for 3 hours at room temperature (20-25C). Alternatively, and sometimes more conveniently, conjugations can be set up and left overnight, as the longer incubation time has no negative effect on the conjugate.
- After incubating for 3 hours (or more), add 1ul of LL-quencher FD reagent for every 10ml of antibody used. The conjugate can be used after 30 minutes.
- Storage of conjugates
For any new conjugate, initial storage at 4C is recommended. A preservative may be desirable
for long-term storage. Other storage conditions (e.g. frozen at -70C or stored at -20C with 50% glycerol) may also be satisfactory. The best conditions for any particular conjugate must be determined by experimentation.
Appendix 1. Compatibility of buffers and buffer additives.
Amine-free buffers, including MES, MOPS, HEPES and phosphate are compatible if they are in the concentration range 10-50mM and have pH values in the range 6.5-8.5, as the addition of LL-Modifier provides the conditions necessary for efficient conjugation. Common non-buffering salts (e.g. sodium chloride), chelating agents (e.g. EDTA), and sugars may be present, as they have no effect on conjugation efficiency. Azide (0.02-0.1%) has little or no effect. If the amine-free buffer is relatively concentrated and outside the pH range 6.6-8.5 you may need to add more LL-modifier for each 10ul of antibody. Excess LL-Modifier is provided so that you can check the pH of the buffer after the addition of the modifier. Ideally the pH should be around 7.3-7.6, though efficient conjugation occurs anywhere between pH 6.8 and 7.8. Avoid buffer components that are nucleophilic, as these may react with Lightning-Link chemicals. Primary amines (e.g. amino acids, ethanolamine) and thiols (e.g. mercaptoethanol, DTT) fall within this class. (Note: Tris has little effect on conjugation efficiency as long as the concentration is 20mM or less).