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Pipa529118

Manufactured by Thermo Fisher Scientific

The PIPA529118 is a laboratory instrument designed for general analytical tasks. It features precision components and advanced technology to provide reliable and consistent performance. The core function of this product is to facilitate various analytical procedures in a laboratory setting.

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2 protocols using pipa529118

1

Immunohistochemical Analysis of COVID-19 Tissues

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4-μm-thick sections were cut from paraffin blocks of lung and liver tissues from COVID-19 patients and non-COVID-19 donors. IHC staining with an anti-FXa protein antibody (PIPA529118, Invitrogen), an anti-furin antibody (ab183495, Abcam), an anti-trypsin antibody (ab200997, Abcam), or an anti-plasmin antibody (LS-C150813–1, LSBio) as a primary antibody was performed by the Pathology Shared Resource Core at City of Hope Beckman Research Institute. Stained slides were mounted and scanned for observation.
Mouse tissues isolated from experimental mice were placed in 10% neutral buffered formalin for a minimum of 72 hours. After paraffin embedding, 4-μm-thick sections were cut from the blocks. H&E staining and IHC with anti-NP protein antibody (NB100–56576, Novus) as the primary antibody were performed by the Pathology Shared Resource Core at City of Hope Beckman Research Institute. Stained slides were mounted and scanned for observation.
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2

Histological Analysis of COVID-19 Tissues

Check if the same lab product or an alternative is used in the 5 most similar protocols
4-μm-thick sections were cut from paraffin blocks of lung and liver tissues from COVID-19 patients and non-COVID-19 donors. The following primary antibodies were used for IHC staining: an anti-FXa protein antibody (PIPA529118, Invitrogen, at a 1:500 dilution), an anti-furin antibody (ab183495, Abcam, at a 1:500 dilution), an anti-trypsin antibody (ab200997, Abcam, at a 1:500 dilution), or an anti-plasmin antibody (LS-C150813-1, LSBio, at a 1:500 dilution). IHC was performed by the Pathology Shared Resource Core at City of Hope Beckman Research Institute. Stained slides were mounted and scanned for observation.
Tissues isolated from the experimental mice were placed in 10% neutral buffered formalin for a minimum of 72 hours. After paraffin embedding, 4-μm-thick sections were cut from the blocks. H&E staining and IHC with an anti-NP protein antibody (NB100-56576, Novus, at a 1:500 dilution) as the primary antibody were performed by the Pathology Shared Resource Core at City of Hope Beckman Research Institute. Stained slides were mounted and scanned for observation.
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