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Horseradish peroxidase hrp conjugated goat anti mouse igg and anti rabbit igg antibodies

Manufactured by Bio-Rad

Horseradish peroxidase (HRP)-conjugated goat anti-mouse IgG and anti-rabbit IgG antibodies are secondary antibodies that can be used for detection in various immunoassays. They are designed to bind to the primary antibodies targeting mouse or rabbit immunoglobulins (IgG) and are conjugated with the enzyme horseradish peroxidase, which can catalyze a colorimetric or chemiluminescent reaction for signal detection.

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3 protocols using horseradish peroxidase hrp conjugated goat anti mouse igg and anti rabbit igg antibodies

1

Maintenance of Mosquito and Mammalian Cell Lines

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Mosquito Aedes albopictus C6/36 cells were maintained at 28°C in Leibovitz medium (L15) supplemented with 10% heat-inactivated fetal bovine serum (FBS). Vero cells and were maintained at 37°C in Dulbecco’s modified Eagle medium (DMEM) supplemented with 5% FBS. BHK-21, SK-N-SH, and HEK-293T cells were maintained at 37°C in DMEM supplemented with 10% FBS. Highly purified mouse anti-pan Flavivirus E monoclonal antibody (mAb) 4G2 was produced by RD Biotech (Besançon, France). Mouse mAb anti-JEV NS5 was kindly provided by Y. Matsuura [26 (link)]. Antibodies against Calnexin and SNAP-tag were purchased from Enzo Life Sciences and New England Biolabs, respectively. Horseradish peroxidase (HRP)-conjugated goat anti-mouse IgG and anti-rabbit IgG antibodies were obtained from Bio-Rad Laboratories. HRP-conjugated goat anti-pig antibody was obtained from Bethyl Laboratories. Alexa Fluor 488-conjugated goat anti-mouse IgG antibody was obtained from Jackson ImmunoResearch.
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2

Antibody Dilutions for HCV Assays

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Mouse monoclonal antibody 9E10 anti-HCV NS5A was kindly provided by Charles Rice38 (link) and diluted 1:1000 in TCID50 assays. Commercial antibodies used in Western blotting, along with their respective dilutions, are listed as follow. Mouse monoclonal antibody anti-HCV NS3 was purchased from Abcam (ab65407, 1:3,000). Mouse monoclonal antibody against GAPDH, rabbit polyclonal antibody against CRBN, and rabbit polyclonal antibody against SOD1 were respectively purchased from GeneTex (GTX28245, 1:5,000), Novus Biologicals (NBP1-91810, 1:500), and Sigma-Aldrich (HPA00140-1; 1:500). Horseradish peroxidase (HRP)-conjugated goat anti-mouse IgG and anti-rabbit IgG antibodies were obtained from Bio-Rad Laboratories (170-6516 and 170-6515, respectively, 1:3,000). IRDye® 800CW-conjugated goat anti-rabbit antibody was purchased from LI-COR (926-32211, 1:10,000).
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3

Antibody Identification and Lipid Staining

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The following commercial antibodies were used: rabbit polyclonal anti-calnexin, anti-PLIN3/TIP47/M6PRBP1 and anti-GFP antibodies from Abcam (Cambridge, UK), and anti-calreticulin antibody from Merck Millipore (Darmstadt, Germany); mouse monoclonal anti-β-tubulin (clone 2-28-33) and anti-c-myc (clone 9E10) antibodies from Sigma (St Louis, MO), anti-Rab8 (clone 4, Rab8), anti-Rab11 (clone 47, Rab11) and anti-GM130 (clone 35, GM130) antibodies from BD Biosciences (Franklin Lakes, NJ), anti-COX IV (clone 1D6E1A8) and anti-transferrin receptor (clone H68.4) antibodies from Life Technologies, anti-β-actin antibody (clone AC-15, Abcam), and anti-PLIN2/ADRP antibody (clone AP 125, PROGEN Biotechnik, Heidelberg, Germany).
The secondary reagents for western blotting were horseradish peroxidase (HRP)-conjugated goat anti-mouse-IgG and anti-rabbit-IgG antibodies (Bio-Rad, Hercules, CA) for analysis of extracts, and HRP–Protein-A (Life Technologies) for immunoprecipitations. The secondary antibodies for immunofluorescence were Alexa Fluor 488, 546 or 647 conjugates of goat anti-mouse-IgG and anti-rabbit-IgG antibodies (Life Technologies).
The following reagents were used: Nile Red, Nocodazole, DAPI and Oil Red O from Sigma; and BODIPY 493/503, BODIPY 558/568 C12 and HCS LipidTOX Red from Life Technologies. Unless otherwise stated, cell culture products were from Life Technologies.
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