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Cy and alexa fluor conjugated secondary antibodies

Manufactured by Jackson ImmunoResearch
Sourced in United States

Cy and Alexa Fluor-conjugated secondary antibodies are fluorescently labeled antibodies that are designed to bind to primary antibodies, enabling detection and visualization of target proteins or molecules in various applications such as immunoassays, flow cytometry, and fluorescence microscopy. These antibodies are available in different fluorescent dye conjugates, providing a range of excitation and emission wavelengths to suit different experimental needs.

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3 protocols using cy and alexa fluor conjugated secondary antibodies

1

Immunocytochemistry Reagent Procurement

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Mouse anti-occludin and rabbit anti-ZO-1 were purchased from Invitrogen. Rabbit anti-cortactin antibody was from Abcam. Rabbit anti-iNOS and eNOS were obtained from Santa Cruz Biotechnology, (Santa Cruz, CA, USA). Mouse anti-prion protein (12F10), for detection of the cellular prion protein was obtained from Cayman (Cayman Chemical, Ann Arbor, MI, USA). Alexa Fluor 488-conjugated phalloidin was purchased from Molecular Probes. Cy and Alexa Fluor-conjugated secondary antibodies were acquired from Jackson Immunoresearch and Molecular Probes, respectively, and used for immunocytochemistry. IR-conjugated secondary antibodies were purchased from LI-COR Biosciences and were used for the in-cell western blot experiments. Unless otherwise mentioned, all other materials used were purchased from Sigma-Aldrich Israel Ltd. (Rehovot, Israel).
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2

Immunocytochemistry Reagents and Protocols

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Mouse anti-VE-cadherin antibody (sc-9989) diluted 1:50 was obtained from Santa Cruz Biotechnology (Dallas, TX, USA). Cy and Alexa Fluor-conjugated secondary antibodies were acquired from Jackson Immunoresearch (Philadelphia, PA, USA) and Molecular Probes (Eugene, OR, USA), respectively, and used for immunocytochemistry. HIF2α inhibitor [51 (link)] (Axon 2034) was obtained from Axon Medchem (Hanzeplein, The Netherlands). Z-VAD-FMK was obtained from Adooq-bioscience (187389-52-2, Irvine, CA, USA) and Santa Cruz Biotechnology (sc-3067, Dallas, TX, USA). Marimastat from Santa Cruz Biotechnology (sc-202223, Dallas, TX, USA), MG-132 from Promega (G9951, Madison, WI, USA). Cytotoxgreen was obtained from Essen BioScience (Ann Arbor, MI, USA) and CellROXgreen from Molecular Probes (Eugene, OR, USA). PX-ethyl was purchased from Sigma (St. Louis, MO, USA). According to the Sigma safety data sheet, safety measures of eye shields, face shields, full-face respirator, and gloves should be taken. PX was used according to our previously reported protocol [43 (link),44 (link)] All other reagents applied in this study were used in accordance to the known literature and the supplier’s guidelines.
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3

Immunocytochemistry with VE-cadherin antibody

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Mouse anti-VE-cadherin antibody (sc-6458) diluted 1:50 was obtained from Santa Cruz Biotechnology (United States). Cy and Alexa Fluor-conjugated secondary antibodies were acquired from Jackson Immunoresearch (United States) and Molecular Probes (United States), respectively, and used for immunocytochemistry. Z-VAD-FMK was obtained from Adooq-bioscience (187389-52-2, United States) and Santa Cruz Biotechnology (sc-3067, United States). Marimastat from Santa Cruz Biotechnology (sc-202223, United States), MG-132 from Promega (G9951, United States). Cytotoxgreen was obtained from Essen BioScience (United States) and CellROXgreen from Molecular Probes (United States). PX-ethyl was purchased from Sigma (United States), according to Sigma safety data sheet safety measures of eyeshields, face shields, full-face respirator and Gloves should be taken. For assessing the BBB response, PX freshly made in ethanol to 400 mM stock solution was immediately diluted in the medium to the desired final concentrations and added to the cell culture. All other reagents applied in this study were used in accordance to the known literature and the supplier's guidelines.
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