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Hrp conjugated species specific secondary antibody

Manufactured by Beyotime
Sourced in China

HRP-conjugated species-specific secondary antibody is a laboratory reagent used in various immunoassays, such as Western blotting and ELISA. It consists of a secondary antibody that is conjugated with the enzyme Horseradish Peroxidase (HRP). This product can be used to detect and quantify target proteins or other biomolecules in a sample by binding to a primary antibody that is specific to the molecule of interest.

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3 protocols using hrp conjugated species specific secondary antibody

1

Protein Expression Analysis in Graft Tissues

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Protein samples were extracted from graft tissues. Equal masses of protein samples were separated by SDS-PAGE, and transferred to PVDF membranes that were blocked and reacted with primary antibodies according to the manufacturer's recommendations. The antibodies used include: CDKN2A (1:600, Abcam), TNFAIP6 (1:800, Abcam), ESR2 (1:400, Abcam), UCN (1:400, LifeSpan BioSciences), IL1B (1:1000, Abcam), VIP (1:1000, Abcam), NFKBIA (1:1000, Abcam), GAL (1:600, Santa), CSF1 (1:400, Santa), JUN (1:1000, Abcam), ARG1 (1:800, Abcam), FGF2 (1:1000, Abcam), ATF3 (1:1000, Abcam), ZFP36 (1:400, Millipore), CCL2 (1:1000, Millipore), GFI1 (1:400, Abcam), CCK (1:1000, Santa), RUNX2 (1:600, Abcam), TNFα (1:600, Abcam), and β-actin (1:4,000, Proteintech). The specific binding of primary antibody was detected by HRP-conjugated species-specific secondary antibody (Beyotime, Shanghai, China) and enhanced chemiluminescence (ECL) assay.
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2

Immunoblotting of Rab GTPases

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Protein samples were extracted from cell cultures. Equal amount of protein samples were separated by SDS-PAGE, and transferred to PVDF membranes, which were blocked, and reacted with primary antibodies against Rab8a (1:1000, Abcam, Cambridge, UK), Rab11a (1 : 500, Abcam), or GAPDH (1:1000, Proteintech, Wuhan, China) according to the manufacturer's recommendations. The specific binding of primary antibody was detected by HRP-conjugated species-specific secondary antibody (Beyotime, Shanghai, China) and enhanced chemiluminescence assay.
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3

Western Blot Analysis of Apoptosis Markers

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Extracted from cell cultures, the protein samples were separated by SDS-PAGE and transferred to the PVDF membranes. According to the manufacturer’s recommendations, the PVDF membranes were then blocked and incubated with the primary antibodies against PAX3 (1:500, Abcam), p53 (1:200, Cell Signaling Technology), Cleaved Caspase-3 (1:500, Cell Signaling Technology), Bcl-2 (1:500, Proteintech) or GAPDH (1:1000, Proteintech). Via HRP-conjugated species-specific secondary antibody (Beyotime, Shanghai, China) and enhanced chemiluminescence assay, the specific binding of primary antibody was finally detected (Zhang et al., 2016 (link)).
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