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Hrp conjugated secondary antibodies

Manufactured by Immunoway
Sourced in United States

HRP-conjugated secondary antibodies are laboratory reagents used in immunoassays and other immunochemical techniques. They consist of a secondary antibody that is covalently linked to the enzyme horseradish peroxidase (HRP). The HRP enzyme can catalyze a colorimetric or chemiluminescent reaction, which allows for the detection and quantification of target analytes in a sample.

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2 protocols using hrp conjugated secondary antibodies

1

Hippocampal Protein Analysis in Mice

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Mice (n = 6 in each group) were decapitated, the hippocampus were immediately dissected, frozen and stored at −80 °C. Tissue samples were lysed and western blots were performed as previously described [11 (link)]. Primary antibodies include GFP (1:1000, Beyotime, cat # AG281, Shanghai, China), Glial fibrillary acidic protein (GFAP) (1:1000, Wanleibio, cat # WL0836, Shenyang, China), Flag (1:1000, abm, cat # G188, Zhenjiang, China), Oligo2 (1:1000, Wanleibio cat # WL04942, Shenyang, China), NeuN (1:1000, Wanleibio, cat # WL03099, Shenyang, China), doublecortin (Dcx) (1:1000, Proteintech, cat # 13925-1-AP, Rosemont, USA), GAPDH (1:5000, Boster, cat # BM1623, Wuhan, China) and β-Tubulin (1:5000, Beidibio, Nanjing, China). HRP-conjugated secondary antibodies purchased from Immunoway Biotechnology Company (goat anti mouse cat # RS0001 and goat anti rabbit cat # RS0002, Plano, TX, USA) were used to probe these blots. Protein visualization was carried out using an enhanced chemiluminescen (ECL, Meilunbio, Dalian, China). The signal intensity was obtained by densitometric scanning.
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2

Western Blot Analysis of Cellular Proteins

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Cell extracts were harvested and separated by SDS-PAGE, and then transferred to PVDF membranes (Millipore, Billerica, USA). The membranes were blocked with 5% non-fat milk for 1 h at room temperature, washed, and incubated with specific antibodies overnight at 4°C. The membranes were washed again and incubated with the corresponding HRP-conjugated secondary antibodies (Immunoway). Finally, protein bands were detected using a chemiluminescence system (Millipore). The primary antibodies used are as follows: anti-FLAG-tag (Cell Signaling Technology), anti-RPA2 (Abcam), anti-β-tubulin (Immunoway), anti-PRIMPOL (Abcam), and anti-RAD51 (Abcam).
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