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Peroxidase affinipure donkey anti rabbit igg h l antibody

Manufactured by Jackson ImmunoResearch

The Peroxidase AffiniPure Donkey Anti-Rabbit IgG (H+L) antibody is a secondary antibody produced in donkeys and specifically recognizes the heavy and light chains of rabbit immunoglobulin G (IgG). The antibody is conjugated with the enzyme horseradish peroxidase (HRP), which can be used as a detection system in various immunoassay techniques.

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2 protocols using peroxidase affinipure donkey anti rabbit igg h l antibody

1

Characterization of HIV Protein Expression

Check if the same lab product or an alternative is used in the 5 most similar protocols
HIV-infected and uninfected H9 cells were pelleted and resuspended in radioimmunoprecipitation assay (RIPA) buffer (25 mM Tris-HCl pH 7.6, 150 mM NaCl, 1% NP-40, 1% sodium deoxycholate, 0.1% SDS) supplemented with protease inhibitor cocktail (Thermo Scientific, cat# 87786). After centrifugation, the protein concentration in the cell lysates was determined using Bicinchoninic acid (BCA) assay (Thermo Scientific, cat# 23235). 1 μg of total protein lysates were resolved on a 4%–12% Bis-Tris gel at 200 V for 30 min. Resolved proteins were transferred to nitrocellulose membranes, blocked and probed with the following primary antibodies: human Fucosyltransferase 7/FUT7 antibody, (clone 795116, R&D Systems, cat# MAB64091), B4GALT5 antibody (Novus, cat# NBP2–14882), GAPDH antibody (clone 14C10, Cell Signaling Technology, cat# 2118), anti-p24 antibody (clone KC57, Beckman Coulter cat# 6604665), and FUT6 Antibody (Thermo Fisher, cat# PA5–96261). After two washes in 1X TBS supplemented with 0.05% Tween 20, membranes were incubated with HRP-conjugated secondary antibody: Peroxidase AffiniPure Donkey Anti-Rabbit IgG (H+L) antibody (Jackson ImmunoResearch, cat# 711-035-152). Bound HRP-conjugated antibodies were revealed with SuperSignal West Pico PLUS chemiluminescent substrate (Thermo Scientific, cat# 34580).
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2

Characterization of HIV Protein Expression

Check if the same lab product or an alternative is used in the 5 most similar protocols
HIV-infected and uninfected H9 cells were pelleted and resuspended in radioimmunoprecipitation assay (RIPA) buffer (25 mM Tris-HCl pH 7.6, 150 mM NaCl, 1% NP-40, 1% sodium deoxycholate, 0.1% SDS) supplemented with protease inhibitor cocktail (Thermo Scientific, cat# 87786). After centrifugation, the protein concentration in the cell lysates was determined using Bicinchoninic acid (BCA) assay (Thermo Scientific, cat# 23235). 1 μg of total protein lysates were resolved on a 4%–12% Bis-Tris gel at 200 V for 30 min. Resolved proteins were transferred to nitrocellulose membranes, blocked and probed with the following primary antibodies: human Fucosyltransferase 7/FUT7 antibody, (clone 795116, R&D Systems, cat# MAB64091), B4GALT5 antibody (Novus, cat# NBP2–14882), GAPDH antibody (clone 14C10, Cell Signaling Technology, cat# 2118), anti-p24 antibody (clone KC57, Beckman Coulter cat# 6604665), and FUT6 Antibody (Thermo Fisher, cat# PA5–96261). After two washes in 1X TBS supplemented with 0.05% Tween 20, membranes were incubated with HRP-conjugated secondary antibody: Peroxidase AffiniPure Donkey Anti-Rabbit IgG (H+L) antibody (Jackson ImmunoResearch, cat# 711-035-152). Bound HRP-conjugated antibodies were revealed with SuperSignal West Pico PLUS chemiluminescent substrate (Thermo Scientific, cat# 34580).
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