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General

You may occasionally observe a small amount of aggregation of the Qdot™ nanocrystals during proper storage. To remove any aggregates that may have formed prior to use, we recommend centrifuging the vial at 2,000 x g for 1 min. Pipette only the supernatant and avoid the pellet. In our experience, pelleting any aggregates that may have formed typically results in a loss of less than 10% of the product.

Once your product undergoes aggregation, it cannot be dispersed back into solution. We recommend purchasing a new product. 

Freezing will cause the product to aggregate. The Qdot™ nanocrystals cannot be dispersed into solution after aggregation.

Appropriate mounting media selection is very important to retain the fluorescence of Qdot™ nanocrystals. In our studies, Qdot™ nanocrystals work best with the following mountants:

  • HistoMount™ medium (Cat No. 00-8030); best for long term archiving
  • Cytoseal™ 60 Mountant
  • Clarion™ Mountant
  • Most polyvinyl alcohol-based mountants (limited storage time, <weeks)
  • Water-based mountants (limited storage time, <week)
  • Up to 50% glycerol (limited storage time, <week)

Note: We do not recommend using ProLong™ mounting media with Qdot™ nanocrystals as it will quench their fluorescence. 

Blinking is an inherent property of quantum dots; in fact, all single-luminescent molecules blink, including organic dyes. The brightness and photostability of Qdot™ nanocrystals makes the blinking more visibly apparent. Under higher energy excitation, Qdot™ nanocrystals blink even faster. Beta-mercaptoethanol can reduce blinking.

The precipitate in the organic ITK™ Qdot™ nanocrystals occurs with some frequency. The ITK™ Qdot™ nanocrystals sometimes include impurities that show as a white precipitate.

Spinning your ITK™ Qdot™ nanocrystals at ~3,000 rpm for 3_5 minutes should remove the white precipitate from the supernatant. Use the supernatant immediately.

Here are some suggestions:

  • Confirm imaging/detection setup suitability. 
    Make sure that you are using an appropriate filter set to detect the signal. Please consult Table 1 in the Qdot™ Biotin User Manual for a list of appropriate and optimal filters. 
  • Check to see that Qdot™ conjugate is fluorescing using an alternative light source.
    Qdot™ conjugates will normally fluoresce brightly under a hand-held ultraviolet lamp (long wave, such as the type used to visualize ethidium bromide on agarose gels). Although we have not seen pronounced loss of fluorescence of these materials under any storage conditions that we have investigated, we have not been able to examine all storage conditions. If the Qdot™ product does not appear to fluoresce under the long wave UV excitation, please contact Technical Support at techsupport@qdots.com. For a microscope, perform a spot test: place a small droplet (2 to 5 μL) of the quantum dot solution onto a clean slide (no coverslip) and examine under the appropriate filter set at low magnification. 
  • Confirm the specificity and titer of primary antibody.
    Make sure the antibody will recognize the intended targets. Make sure there is sufficient primary antibody bound to the targets. This verification can be performed by ELISA-based capture of the antigen of interest, or by other techniques that can be found in lab manuals such as the Current Protocols in Immunology. 
  • For Qdot™ streptavidin conjugates, confirm biotinylation of antibody.
    Make sure your antibodies are effectively biotinylated. It may be necessary to independently adjust the concentration of both the primary and secondary antibodies used in the assay to obtain optimal signal and minimal background. 
  • PAP pen ink may quench signal.
    Use an alternate method for isolating target areas on the slide. If your protocol requires the use of a PAP pen, we recommend the ImmEdge™ Hydrophobic Barrier Pen (Cat. No. H-4000) from Vector Labs. 

Here are some suggestions:

  • Use the Qdot™ Incubation Buffer (Cat. No. Q20001MP).
    The included buffer is formulated specifically for improved signal-to-background ratios in most immunolabeling applications using the Qdot™ streptavidin conjugates. Alternate buffers may result in more variable staining and, in particular, may increase background staining. However, some specific applications may require other buffer conditions. Please see the protocol "Double-labeling Using Qdot™ Streptavidin conjugates." 
  • Determine if the sample has a high level of endogenous biotin. Block the sample using an avidin-biotin pre-blocking step.
    If you have used the Qdot™ Incubation Buffer and still get high nonspecific background, then it may be necessary to check other steps of your procedure. Blocking the sample with BSA or normal animal serum will generally decrease nonspecific binding of both antibodies and Qdot™ streptavidin conjugates. It is a good practice to dilute your primary and secondary antibodies in the blocking buffer. Some tissues such as spleen and kidney sections may contain endogenous biotin, which may contribute to non-specific signal. Endogenous biotin can be blocked with an avidin/biotin blocking kit (Cat. No. E21390). 
  • Grainy staining or clumps of fluorescent material appear in the background.
    Occasionally the BSA within the Qdot™ Incubation Buffer shows slight aggregation over time. It is necessary to remove this aggregate prior to labeling the sample with the Qdot™ streptavidin conjugate. Spin down the incubation mixture before addition to the sample. This can be accomplished by spinning the samples in a benchtop centrifuge (Eppendorf 5415) at 5,000 x g for 2 minutes. The material can also be passed over a 0.2 µm spin filter unit before you add it to the sample for staining to remove microscopic precipitates. If you are using a buffer that is different than the Qdot™ Incubation Buffer, this behavior can often be attributed to higher levels of NaCl or other salts in the incubation buffer, and may not be easily fixed with filtration. In this case, reduce the overall salt concentration. 
  • Optimize concentration of biotinylated secondary antibodies.
    Optimizing specific signal can often be achieved by adjusting the level of biotinylated antibody used instaining. High levels of biotinylated antibody are necessary to obtain specific labeling, but overly high levels will contribute to nonspecific binding of the antibody to the sample. Nonspecifically bound biotinylated antibody will bind to the Qdot™ streptavidin conjugate, resulting in higher staining of the background.
  • Optimize concentration of Qdot™ streptavidin conjugate.
    Just as titration of primary and secondary antibodies is necessary to achieve optimal specific signal in immunolabeling applications, the level of the final probe should be optimized for each conjugate. In general, concentrations at or slightly below saturation should have the optimal signal-to-background ratio, while concentrations substantially higher than saturation will compromise the assay with higher background levels. 

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