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Alliance hiv 1 p24 antigen elisa kit 96 test

Manufactured by PerkinElmer

The Alliance HIV-1 P24 Antigen ELISA Kit [96 Test] is a laboratory equipment product designed for the detection and quantification of the HIV-1 p24 antigen in biological samples. It utilizes the enzyme-linked immunosorbent assay (ELISA) technique to provide a reliable and standardized method for measuring the presence of the HIV-1 p24 antigen.

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2 protocols using alliance hiv 1 p24 antigen elisa kit 96 test

1

In Vivo Biodistribution of Transduced BM Cells

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For in vivo biodistribution studies, 4 × 105 Lin BM cells from male and female P3D2F1 mice transduced with PGK-coRPK-WPRE LV were intravenously administered into lethally irradiated B6D2F1 congenic recipients of both sexes. Results were compared with a control group that received non-transduced cells (n = 6 male, and n = 2 females). 1 month after BM transplantation (see Table S1), mice were sacrificed by anesthetic overdose with Avertin (15 μL of a 2.5% solution/1 g weight). Animals were perfused with PBS/EDTA solution through a cardiac cannula and hematopoietic (PB, BM, spleen, thymus, LNs), and non-hematopoietic (liver, lung, kidney, pancreas, large and small intestine, stomach, gonads, brain, muscle, heart) organs were extracted and processed for histology, flow cytometry, analysis of VCN, and serology for the presence of HIV p24 protein, measured according to the manufacturer’s instructions (Alliance HIV-1 P24 Antigen ELISA Kit [96 Test] [NEK050001KT]; PerkinElmer) (see Supplemental text).
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2

Vaginal HIV-1 Challenge in Mouse Model

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Vaginal drug administration was carried out as described previously25 ,27 (link) and summarized in Fig. 1. The employed drug concentrations in the single- and multiple drug dosing groups are provided in Supplementary Data S1S4. Stocks of HIV-1 JR-CSF were prepared as previously described28 (link),37 (link) and standardized by p24 ELISA using the Alliance HIV-1 P24 ANTIGEN ELISA Kit (96 Test) (Perkin Elmer, Waltham, MA), according to the manufacturer’s instructions. Prior to inoculation, mice were anesthetized with isoflurane. Aliquots (5 μL) of drug solutions in PBS were applied vaginally through a pipet tip. The rear half of the mouse remained elevated during the procedure to reduce chance of back-flow from the vaginal cavity during the recovery. Within 30 min (typically 15–25 min) post-drug application, mice were vaginally challenged with HIV-1 (5 µL, corresponding to 200 ng of p24). This inoculum is a standard high viral load for successful vaginal infection (1 ng of p24 corresponds to ca. 10 infectious units). Methods used for the atraumatic vaginal HIV-1 challenge are described elsewhere38 (link),41 (link)–44 (link).
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