- /content/site/us/en/home/References/Molecular-Probes-The-Handbook/tables/Spectral-characteristics-of-PeakFlow-flow-cytometry-reference-beads
- Molecular Probes amine-reactive dyes—Table 1.1
- Active esters and kits for labeling proteins and nucleic acids—Table 1.2
- Molecular Probes kits for protein and nucleic acid labeling—Table 1.3
- Alexa Fluor active esters and kits for labeling proteins and nucleic acids—Table 1.4
- Fluorescence quantum yields (QY) and lifetimes (τ) for Alexa Fluor dyes—Table 1.5
- R<0> values for some Alexa Fluor dyes—Table 1.6
- Amine-reactive BODIPY dyes—Table 1.7
- Amine-reactive xanthene derivatives in this section—Table 1.8
- Amine-reactive, orange- and red-fluorescent fluorophores in this section—Table 1.9
- Molecular Probes nonfluorescent quenchers and photosensitizers—Table 1.10
- R<0> values for QSY and dabcyl quenchers—Table 1.11
- Amine-reactive, ultraviolet light–excitable fluorophores for labeling proteins and nucleic acids—Table 1.12
- Amine-reactive, environment-sensitive fluorophores—Table 1.13
- Molecular Probes thiol-reactive dyes excited with visible light—Table 2.1
- Molecular Probes thiol-reactive dyes excited with ultraviolet light—Table 2.2
- Molecular Probes azide and alkyne derivatives—Table 3.1
- Molecular Probes hydrazine, hydroxylamine and amine derivatives—Table 3.2
- Biotinylation and desthiobiotinylation reagents—Table 4.1
- Selected haptenylation reagents and their anti-hapten antibodies—Table 4.2
- Sensitivity of the FluoReporter Biotin Quantitation Assay Kit for biotinylated nucleic acids with varying degrees of biotinylation—Table 4.3
- Molecular Probes heterobifunctional crosslinkers—Table 5.1
- Properties of six different caging groups—Table 5.2
- Tyramide Signal Amplification (TSA) Kits—Table 6.1
- Spectral data for B-PE, R-PE and APC—Table 6.2
- Tandem conjugates of R-phycoerythrin (R-PE)—Table 6.3
- Tandem conjugates of allophycocyanin (APC)—Table 6.4
- Molecular Probes yellow-green–fluorescent FluoSpheres beads compared with other commercially available yellow-green–fluorescent microspheres—Table 6.5
- Fluorescein equivalents in Molecular Probes yellow-green–fluorescent FluoSpheres beads—Table 6.6
- Summary of FluoSpheres fluorescent microspheres—Table 6.7
- Summary of biotin-, streptavidin- and NeutrAvidin biotin-binding protein–labeled FluoSpheres microspheres—Table 6.8
- Summary of TransFluoSpheres fluorescent microspheres—Table 6.9
- Extinction coefficients of Qdot nanocrystal streptavidin conjugates at ultraviolet and visible wavelengths—Table 6.10
- Qdot nanocrystal secondary antibody conjugates—Table 6.11
- Qdot nanocrystal anti–human CD antibody conjugates—Table 6.12
- Summary of Molecular Probes secondary antibody conjugates—Table 7.1
- Alkaline phosphatase and horseradish peroxidase enzyme conjugates—Table 7.4
- Molecular Probes goat anti-mouse isotype-specific antibodies—Table 7.5
- Fluorescent dyes successfully tested with the Image-iT FX signal enhancer—Table 7.8
- NANOGOLD, Alexa Fluor FluoroNanogold and colloidal gold conjugates—Table 7.10
- Binding profiles of protein A and protein G—Table 7.12
- Zenon Antibody Labeling Kits—Table 7.14
- Anti-fluorophore and anti-hapten antibodies—Table 7.19
- Molecular Probes avidin, streptavidin, NeutrAvidin and CaptAvidin conjugates—Table 7.23
- Molecular Probes lectin conjugates—Table 7.24
- Specialty nucleic acid reagents for molecular biology—Table 8.1
- Cell membrane–impermeant cyanine nucleic acid stains—Table 8.2
- Cell-permeant cyanine nucleic acid stains—Table 8.3
- Properties of classic nucleic acid stains—Table 8.4
- Molecular Probes ChromaTide and aha labeled nucleotides—Table 8.5
- Molecular Probes nucleic acid labeling kits—Table 8.6
- Amine-reactive dyes for nucleic acid sequencing—Table 8.7
- Selection guide for the Qubit and Quant-iT Assay Kits—Table 8.8
- A comparison of reagents for detecting and quantitating proteins in solution—Table 9.1
- SYPRO and Coomassie Fluor luminescent and fluorescent protein gel stains—Table 9.2
- Molecular Probes fluorescent and luminescent protein blot stains—Table 9.3
- Pro-Q Diamond gel stain reagents and kits—Table 9.4
- Pro-Q Emerald glycoprotein stain kits for gels and for blots—Table 9.5
- Glycosidase enzymes and their fluorogenic and chromogenic substrates—Table 10.1
- Rhodamine 110–based bis-peptide substrates—Table 10.2
- RediPlate Assay Kits—Table 10.3
- Detection limits of the EnzChek Protease Assay Kits—Table 10.4
- Advantages of the Amplex UltraRed reagent over chromogenic reagents—Table 10.5
- CellLight reagents and their targeting sequences—Table 11.1
- Spectral characteristics of Molecular Probes actin-selective probes—Table 11.2
- Molecular Probes fluorescent organelle stains—Table 12.1
- Spectral characteristics of the MitoTracker probes—Table 12.2
- Summary of our LysoTracker and LysoSensor probes—Table 12.3
- Phospholipids with labeled head groups—Table 13.1
- Spectral properties of some lipid probes—Table 13.2
- Techniques for loading molecules into the cytoplasm—Table 14.1
- Fluorescence characteristics of NeuroTrace fluorescent Nissl stains—Table 14.2
- Summary of our lipophilic carbocyanine and aminostyryl tracers—Table 14.3
- Molecular Probes dextran conjugates—Table 14.4
- FluoSpheres microspheres for blood flow determination—Table 14.5
- FluoSpheres blood flow and color kits—Table 14.6
- FluoSpheres and TransFluoSpheres microspheres for tracing—Table 14.7
- Molecular Probes europium and platinum luminescent FluoSpheres microspheres—Table 14.8
- Esterase substrates for cell viability studies—Table 15.1
- Molecular Probes assay kits for cell viability, cell counting and bacterial gram staining—Table 15.2
- Some organisms that have been successfully stained with our LIVE/DEAD BacLight Bacterial Viability Kits—Table 15.3
- Molecular Probes apoptosis assay kits—Table 15.4
- Fluorogenic substrates for caspase activity—Table 15.5
- Fluorescent detection reagents for imaging mitochondria and lysosomes—Table 15.6
- Fluorescent lipopolysaccharide conjugates—Table 16.1
- Transferrin conjugates—Table 16.2
- BioParticles fluorescent bacteria and yeast—Table 16.3
- Labeled and unlabeled alpha-bungarotoxins—Table 16.4
- Invitrogen kinase assay platforms—Table 17.1
- Spectroscopic properties of MANT-ATP in aqueous solution (pH 8)—Table 17.2
- Fluorescence-based phospholipase assays—Table 17.3
- Reactive oxygen species—Table 18.1
- Scavengers of reactive oxygen species (ROS)—Table 18.2
- Tetrazolium salts for detecting redox potential in living cells and tissues—Table 18.3
- Fluorescence response of APF, HPF and H2DCFDA to various reactive oxygen species (ROS)—Table 18.4
- Summary of Molecular Probes fluorescent Ca2+ indicators—Table 19.1
- Comparison of in vitro and in situ Kd values for various Ca2+ indicators—Table 19.2
- Parallel performance comparison of fluo-3 and fluo-4 on Molecular Devices FLIPR system—Table 19.3
- Coelenterazines and their properties—Table 19.4
- Response of fura-2 and indo-1 to some divalent cations other than Ca2+ and Mg2+—Table 19.5
- Fluorescent indicators for Zn2+—Table 19.6
- Ca2+ affinities of BAPTA chelators—Table 19.7
- Molecular Probes pH indicator families, in order of decreasing pKa—Table 20.1
- Summary of the pH response of our LysoSensor probes—Table 20.2
- Molecular Probes pH indicator dextrans, in order of decreasing pKa—Table 20.3
- Reactive pH indicator dyes—Table 20.4
- Characteristics and selected applications of Molecular Probes fast-response probes—Table 22.1
- Characteristics and selected applications of Molecular Probes slow-response probes—Table 22.2
- Spectral characteristics of Molecular Probes dyes—Table 23.1
- Fluorescence excitation sources—Table 23.2
- Contents of FocalCheck fluorescence microscope test slides—Table 23.3
- Spectroscopic data for components of the Reference Dye Sampler Kit—Table 23.4
- CultureWell cell culture systems and chambered coverslips—Table 23.5
- CoverWell chamber gaskets—Table 23.6
- Press-to-Seal gaskets and Secure-Seal spacers—Table 23.7
- Tools for hybridization experiments—Table 23.8
- Spectral characteristics of PeakFlow flow cytometry reference beads—Table 23.9
Spectral characteristics of PeakFlow flow cytometry reference beads—Table 23.9
| Cat # | Size (µm) | Nominal Color | Abs * (nm) | Em * (nm) | Emission Matches Cells Stained with: |
|---|---|---|---|---|---|
| P14825 | 2.5 | Blue | 400 † | 460 | DAPI, Hoechst dyes |
| P14826 | 6.0 | ||||
| P14827 | 2.5 | Green | 505 ‡ | 515 | Fluorescein, Alexa Fluor 488 dye, Oregon Green 488 dye, DiOC18(3) ("DiO") |
| P14828 | 6.0 | ||||
| P14829 | 2.5 | Orange | 570 ‡ | 575 | R-phycoerythrin, tetramethylrhodamine, Alexa Fluor 568 dye, DiIC18(3) ("DiI") |
| P14830 | 6.0 | ||||
| P14831 | 2.5 | Carmine | 580 ‡ | 620 | Propidium iodide, Texas Red dye, Alexa Fluor 594 dye |
| P14832 | 6.0 | ||||
| P24670 | 6.0 | Claret | 645 § | 680 | TOTO-3, Alexa Fluor 647 dye, Cy5 dye, DiIC18(5) ("DiD") |
| P24671 | 6.0 | Ultra red | 665 § | 695 | Alexa Fluor 660 dye, Cy5.5 dye |
| P24672 | 6.0 | Infrared | 735 | 770 | Alexa Fluor 750 dye, Cy7 dye, DiIC18(7) ("DiR") |
| * Approximate absorption and emission maxima for beads in suspension. † Suitable for excitation by the UV (351–364 nm) spectral line of argon-ion lasers. ‡ Suitable for excitation by the 488 nm spectral line of argon-ion lasers. § Suitable for excitation by the 633 nm spectral line of He-Ne lasers. | |||||
