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Ranking of fluorochromes - not instrument specific (specific soon to be uploaded on instrument configurations)

Very BrightBrightOkayDim
PEAPCR700BV510APCCY7
PECF594BUV661BUV395DYLIGHT800
PEDAZZLE594BV605FITCAPCH7
PECY7BUV737PERCPCY55AF700
PECY55APCBUV496PERCP
BB515AF647AF488APCFIRE
BV421BV786BV570V500
BV650APCR700
PB
BV711BV750
V450
BB700BV480
BUV805
BYG584BUV615

BB790BUV563

PECY5


BB630




BB660






Clone selection...

Ensure antibody clone / manufacturer differences are tested when selecting antibodies for a panel.

a)Image Added

b)Image Added

(a) Two clones were available for the transcription factor PU.1 (found in some myeloid cell subsets). Both are on the same fluorophore, but only clone 7C6B05 was able to resolve a separate population. A titration was preformed, but the population was never discernible by clone 7C2C34.

(b) Here the same clone from two different companies on two similar fluorophores was evaluated on the same PBMC donor. You can see company A conjugated-antibody was able to resolve a CD3+ CRTH2+ population, however company B’s conjugated antibody was not. Increasing the concentration did not help and simply resulted in more spread in the negative.

Viability titration

Benefits of titrating not only antibodies but viability dyes. 

Image Added

(above) Titration revealing populations that are unresolvable with an abundance of antibody due to non-specific binding.

(below) Often overlooked, titrating the amine-reactive viability markers can result in tighter negative populations due to minimised unbound fluorophores and baseline restoration, which has less of an effect on other important markers even in the negative (live) population.  

Annotate your experiment before or during data acquisition

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