24 Diagnostic Applications of Phycobiliproteins
609
Gratama, J. W., D’hautcourt, J. L., Mandy, F., Rothe, G., Barnett, D., Janossy, G., et al. (1998). Flow
cytometric quantitation of immunofluorescence intensity: Problems and perspectives. Cytometry,
33, 166–178.
Gupta, R., Jain, P., Deo, S. V. S., & Sharma, A. (2004). Flow cytometric analysis of CD5+ B cells:
A frame of reference for minimal residual disease analysis in chronic lymphocytic leukemia.
American Journal of Clinical Pathology, 121, 368–372.
Hasper, H. J., Weghorst, R. M., Richel, D. J., Meerwaldt, J. H., Olthuis, F. M. F. G., & Schenkeveld,
C. E. I. (2000). A new four-color flow cytometric assay to detect apoptosis in lymphocyte subsets
of cultured peripheral blood cells. Cytometry, 40, 167–171.
Leigh, D. R., Steinert, S., Moore, L. R., Chalmers, J. J., & Zborowski, M. (2005). Cell tracking
velocimetry as a tool for defining saturation binding of magnetically conjugated antibodies.
Cytometry A, 66, 103–108.
Lin, Z., Jiang, B. P., Liang, J., Wen, C., & Shen, X. C. (2019). Phycocyanin functionalized
single-walled carbon nanohorns hybrid for near-infrared light-mediated cancer phototheranostics.
Carbon, 143, 814–827.
Ma, H. J., Zhao, G., Zi, S. X., Li, D. G., Liu, W., & Yang, Q. Q. (2010). Efficacy of quantifying
melanosome transfer with flow cytometry in a human melanocyte–HaCaT keratinocyte co-culture
system in vitro. Experimental Dermatology, 19(8), e282–e285.
Moss, D. M., & Arrowood, M. J. (2001). Quantification of Cryptosporidium parvum oocysts in
mouse fecal specimens using immunomagnetic particles and two-color flow cytometry. Journal
of Parasitology, 87, 406–413.
Nagy, S., Jansen, J., Topper, E. K., & Gadella, B. M. (2003). A triple-stain flow cytometric method
to assess plasma-and acrosome-membrane integrity of cryopreserved bovine sperm immediately
after thawing in presence of egg-yolk particles. Biology of Reproduction, 68, 1828–1835.
Onlamoon, N., Tabprasit, S., Sukapirom, K., Polsira, K., Ammaranond, P., Loharungsikul, S., et al.
(2011). Discordant CD38 measurement of CD8+ T lymphocytes using fluorescein conjugates in
comparison with phycoerythrin conjugates. Asian Pacific Journal of Allergy and Immunology,
29, 181.
Opalka, D., Lachman, C. E., MacMullen, S. A., Jansen, K. U., Smith, J. F., Chirmule, N., et al.
(2003). Simultaneous quantitation of antibodies to neutralizing epitopes on virus-like particles
for human papillomavirus types 6, 11, 16, and 18 by a multiplexed luminex assay. Clinical and
Diagnostic Laboratory Immunology, 10, 108–115.
Pan, Y., Wei, X., Liang, T., Zhou, J., Wan, H., Hu, N., et al. (2018). A magnetic beads-based portable
flow cytometry immunosensor for in-situ detection of marine biotoxin. Biomedical Microdevices,
20, 60.
Pannu, K. K., Joe, E. T., & Iyer, S. B. (2001). Performance evaluation of QuantiBRITE phycoerythrin
beads. Cytometry, 45, 250–258.
Patel, D., & Good, T. (2007). A rapid method to measure beta-amyloid induced neurotoxicity
in vitro. Journal of Neuroscience Methods, 161, 1–10.
Ramachandiran, V., Grigoriev, V., Lan, L., Ravkov, E., Mertens, S. A., & Altman, J. D. (2007). A
robust method for production of MHC tetramers with small molecule fluorophores. Journal of
Immunological Methods, 319, 13–20.
Ritzi-Lehnert, M., Himmelreich, R., Attig, H., Claußen, J., Dahlke, R., Großhauser, G., et al. (2011).
On-chip analysis of respiratory viruses from nasopharyngeal samples. Biomedical Microdevices,
13, 819–827.
Stuchlý, J., Kanderová, V., Fišer, K., ˇ
Cerná, D., Holm, A., Wu, W., et al. (2012). An automated
analysis of highly complex flow cytometry-based proteomic data. Cytometry A, 81, 120–129.
Subires, A., Yuste, J., & Capellas, M. (2014). Flow cytometry immunodetection and membrane
integrity assessment of Escherichia coli O157: H7 in ready-to-eat pasta salad during refrigerated
storage. International Journal of Food Microbiology, 168, 47–56.
Tawa, K., Yamamura, S., Sasakawa, C., Shibata, I., & Kataoka, M. (2016). Sensitive detection of cell
surface membrane proteins in living breast cancer cells using multicolor fluorescence microscopy
with a plasmonic chip. ACS Applied Materials & Interfaces, 8, 29893–29898.
609
Gratama, J. W., D’hautcourt, J. L., Mandy, F., Rothe, G., Barnett, D., Janossy, G., et al. (1998). Flow
cytometric quantitation of immunofluorescence intensity: Problems and perspectives. Cytometry,
33, 166–178.
Gupta, R., Jain, P., Deo, S. V. S., & Sharma, A. (2004). Flow cytometric analysis of CD5+ B cells:
A frame of reference for minimal residual disease analysis in chronic lymphocytic leukemia.
American Journal of Clinical Pathology, 121, 368–372.
Hasper, H. J., Weghorst, R. M., Richel, D. J., Meerwaldt, J. H., Olthuis, F. M. F. G., & Schenkeveld,
C. E. I. (2000). A new four-color flow cytometric assay to detect apoptosis in lymphocyte subsets
of cultured peripheral blood cells. Cytometry, 40, 167–171.
Leigh, D. R., Steinert, S., Moore, L. R., Chalmers, J. J., & Zborowski, M. (2005). Cell tracking
velocimetry as a tool for defining saturation binding of magnetically conjugated antibodies.
Cytometry A, 66, 103–108.
Lin, Z., Jiang, B. P., Liang, J., Wen, C., & Shen, X. C. (2019). Phycocyanin functionalized
single-walled carbon nanohorns hybrid for near-infrared light-mediated cancer phototheranostics.
Carbon, 143, 814–827.
Ma, H. J., Zhao, G., Zi, S. X., Li, D. G., Liu, W., & Yang, Q. Q. (2010). Efficacy of quantifying
melanosome transfer with flow cytometry in a human melanocyte–HaCaT keratinocyte co-culture
system in vitro. Experimental Dermatology, 19(8), e282–e285.
Moss, D. M., & Arrowood, M. J. (2001). Quantification of Cryptosporidium parvum oocysts in
mouse fecal specimens using immunomagnetic particles and two-color flow cytometry. Journal
of Parasitology, 87, 406–413.
Nagy, S., Jansen, J., Topper, E. K., & Gadella, B. M. (2003). A triple-stain flow cytometric method
to assess plasma-and acrosome-membrane integrity of cryopreserved bovine sperm immediately
after thawing in presence of egg-yolk particles. Biology of Reproduction, 68, 1828–1835.
Onlamoon, N., Tabprasit, S., Sukapirom, K., Polsira, K., Ammaranond, P., Loharungsikul, S., et al.
(2011). Discordant CD38 measurement of CD8+ T lymphocytes using fluorescein conjugates in
comparison with phycoerythrin conjugates. Asian Pacific Journal of Allergy and Immunology,
29, 181.
Opalka, D., Lachman, C. E., MacMullen, S. A., Jansen, K. U., Smith, J. F., Chirmule, N., et al.
(2003). Simultaneous quantitation of antibodies to neutralizing epitopes on virus-like particles
for human papillomavirus types 6, 11, 16, and 18 by a multiplexed luminex assay. Clinical and
Diagnostic Laboratory Immunology, 10, 108–115.
Pan, Y., Wei, X., Liang, T., Zhou, J., Wan, H., Hu, N., et al. (2018). A magnetic beads-based portable
flow cytometry immunosensor for in-situ detection of marine biotoxin. Biomedical Microdevices,
20, 60.
Pannu, K. K., Joe, E. T., & Iyer, S. B. (2001). Performance evaluation of QuantiBRITE phycoerythrin
beads. Cytometry, 45, 250–258.
Patel, D., & Good, T. (2007). A rapid method to measure beta-amyloid induced neurotoxicity
in vitro. Journal of Neuroscience Methods, 161, 1–10.
Ramachandiran, V., Grigoriev, V., Lan, L., Ravkov, E., Mertens, S. A., & Altman, J. D. (2007). A
robust method for production of MHC tetramers with small molecule fluorophores. Journal of
Immunological Methods, 319, 13–20.
Ritzi-Lehnert, M., Himmelreich, R., Attig, H., Claußen, J., Dahlke, R., Großhauser, G., et al. (2011).
On-chip analysis of respiratory viruses from nasopharyngeal samples. Biomedical Microdevices,
13, 819–827.
Stuchlý, J., Kanderová, V., Fišer, K., ˇ
Cerná, D., Holm, A., Wu, W., et al. (2012). An automated
analysis of highly complex flow cytometry-based proteomic data. Cytometry A, 81, 120–129.
Subires, A., Yuste, J., & Capellas, M. (2014). Flow cytometry immunodetection and membrane
integrity assessment of Escherichia coli O157: H7 in ready-to-eat pasta salad during refrigerated
storage. International Journal of Food Microbiology, 168, 47–56.
Tawa, K., Yamamura, S., Sasakawa, C., Shibata, I., & Kataoka, M. (2016). Sensitive detection of cell
surface membrane proteins in living breast cancer cells using multicolor fluorescence microscopy
with a plasmonic chip. ACS Applied Materials & Interfaces, 8, 29893–29898.