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Anti rabbit igg hrp conjugate

Manufactured by Agilent Technologies
Sourced in United States

The Anti-rabbit IgG HRP conjugate is a reagent used in immunoassays and Western blotting applications. It consists of horseradish peroxidase (HRP) enzyme covalently conjugated to anti-rabbit immunoglobulin G (IgG) antibodies. This conjugate can be used to detect and quantify the presence of rabbit IgG in biological samples.

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2 protocols using anti rabbit igg hrp conjugate

1

Peptide-based Epitope Mimic Library

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A library of peptide based epitope mimics was synthesized using solid-phase Fmoc synthesis. An amino functionalized polypropylene support was obtained by grafting with a proprietary hydrophilic polymer formulation, followed by reaction with t-butyloxycarbonyl-hexamethylenediamine (BocHMDA) using dicyclohexylcarbodiimide (DCC) with N-hydroxybenzotriazole (HOBt) and subsequent cleavage of the Boc-groups using trifluoroacetic acid (TFA). Standard Fmoc-peptide synthesis was used to synthesize peptides on the amino-functionalized solid support by custom modified JANUS liquid handling stations (Perkin Elmer). The binding of antibody to each of the synthesized peptides was tested in a pepscan-based ELISA. The peptide arrays were incubated with primary antibody solution (overnight at 4 °C). After washing, the peptide arrays were incubated with a 1:1000 dilution of anti-rabbit IgG HRP conjugate (DAKO) for 1 h at 25 °C. After washing, the peroxidase substrate 2,2′-azino-di-3-ethylbenzthiazoline sulfonate (ABTS) and 20 μl/ml of 3% H2O2 were added. After 1 h, the color development was measured with a charge coupled device (CCD) - camera and an image processing system. Epitope targets were read as the largest contiguous stretch of amino acids shared by all peptides recognized by the primary antibodies.
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2

Western Blot Analysis of Phospho-STAT3

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Cells were resuspended in ice-cold lysis buffer (50 mM Tris, 150 mM NaCl, 10% glycerol, 1% IGEPAL CA-630, 0.5% sodium deoxycholate, 0.1% SDS, 10 mM NaF, 1.5 mM Na 3 VO 4 and 1 mM EDTA), supplemented with SIGMAFAST protease inhibitors (Sigma-Aldrich) and benzonase (Merck Millipore, Billerica, MA, USA, 25 U per cell pellet), and lysed for 30 min at 4 °C with rotation. Samples were then centrifuged at 17 000 g for 20 min at 4 °C. Supernatants were assayed for protein concentration using the Pierce 660 nm protein assay and diluted to the same protein concentration with lysis buffer. Aliquots corresponding to 10 μg of cell protein were diluted with 5 × SDS-PAGE sample buffer, heated to 95 °C for 10 min and centrifuged at 12 000 g for 5 min at room temperature. Samples were run on a 10% SDS-PAGE gel, transferred to polyvinylidene difluoride and analyzed by immunoblot using polyclonal rabbit antibody raised against mouse phospho-STAT3 (Cell Signaling, Danvers, MA, USA), mouse monoclonal antibody raised against beta actin (Abcam, Cambridge, MA, USA), anti-mouse IgG, HRP conjugate (Promega, Fitchburg, WI, USA) and anti-rabbit IgG, HRP conjugate (Dako, Carpinteria, CA, USA).
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