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Fluorescein cadaverine

Manufactured by Thermo Fisher Scientific
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Fluorescein cadaverine is a fluorescent dye that can be used as a labeling reagent in various analytical and research applications. It is a derivative of the fluorescent compound fluorescein, which contains a cadaverine linker. The core function of fluorescein cadaverine is to provide a fluorescent label that can be attached to molecules or structures of interest for detection and analysis purposes.

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Lab products found in correlation

Trypsin edta, by Thermo Fisher Scientific (2 mentions) Sodium pyruvate, by Thermo Fisher Scientific (2 mentions) L glutamine, by Thermo Fisher Scientific (2 mentions) Matrigel, by BD (2 mentions) Dulbecco s modified eagle s medium, by Thermo Fisher Scientific (2 mentions) Anti green fluorescent protein, by Abcam (2 mentions) Anti tg2 mab3839, by Merck Group (2 mentions) Biocoat cell inserts, by BD (2 mentions) Cell lysis buffer 9803, by Cell Signaling Technology (2 mentions)

2 protocols using fluorescein cadaverine

1

Inhibiting Transglutaminase 2 Activity

Check if the same lab product or an alternative is used in the 5 most similar protocols
Dulbecco's modified Eagle's medium (11960-077), sodium pyruvate (11360-070), L-Glutamine (25030-164), and 0.25% trypsin-EDTA (25200-056) were from Gibco. Heat-inactivated FCS (F4135), anti–β-actin (A5441), A23187 ionophore was from Sigma (C7522). Anti-green fluorescent protein was from Abcam (ab290). Cell lysis buffer (9803) was from Cell Signaling Technology. Anti-TG2 (MAB3839) was from EMD Millipore. Synthesis of the NC9, and CP4d TG2 inhibitors is described elsewhere (31 , 44 (link)). VA4 and VA5 were synthesized by Akbar and Keillor (unpublished). Fluorescein cadaverine (FC) was from Life Technologies. BD Biocoat cell inserts (353097) and Matrigel (354234) were from BD Biosciences. Measurement of significant difference was performed using the student’s T test with a minimum of three independent repeated experiments.
Kerr C., Szmacinski H., Fisher M.L., Nance B., Lakowicz J.R., Akbar A., Keillor J.W., Wong T.L., Godoy-Ruiz R., Toth E.A., Weber D.J, & Eckert R.L. (2016). Transamidase site-targeted agents alter the conformation of the transglutaminase cancer stem cell survival protein to reduce GTP binding activity and cancer stem cell survival. Oncogene, 36(21), 2981-2990.
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2

Inhibiting Transglutaminase 2 Activity

Check if the same lab product or an alternative is used in the 5 most similar protocols
Dulbecco's modified Eagle's medium (11960-077), sodium pyruvate (11360-070), L-Glutamine (25030-164), and 0.25% trypsin-EDTA (25200-056) were from Gibco. Heat-inactivated FCS (F4135), anti–β-actin (A5441), A23187 ionophore was from Sigma (C7522). Anti-green fluorescent protein was from Abcam (ab290). Cell lysis buffer (9803) was from Cell Signaling Technology. Anti-TG2 (MAB3839) was from EMD Millipore. Synthesis of the NC9, and CP4d TG2 inhibitors is described elsewhere (31 , 44 (link)). VA4 and VA5 were synthesized by Akbar and Keillor (unpublished). Fluorescein cadaverine (FC) was from Life Technologies. BD Biocoat cell inserts (353097) and Matrigel (354234) were from BD Biosciences. Measurement of significant difference was performed using the student’s T test with a minimum of three independent repeated experiments.
Kerr C., Szmacinski H., Fisher M.L., Nance B., Lakowicz J.R., Akbar A., Keillor J.W., Wong T.L., Godoy-Ruiz R., Toth E.A., Weber D.J, & Eckert R.L. (2016). Transamidase site-targeted agents alter the conformation of the transglutaminase cancer stem cell survival protein to reduce GTP binding activity and cancer stem cell survival. Oncogene, 36(21), 2981-2990.
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