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Hrp conjugated anti rabbit igg secondary antibody

Manufactured by CWBIO

The HRP-conjugated anti-rabbit IgG secondary antibody is a laboratory tool used to detect and quantify the presence of rabbit primary antibodies in various immunoassays. It consists of an anti-rabbit IgG antibody that is conjugated with the enzyme Horseradish Peroxidase (HRP). This secondary antibody can bind to the constant region of rabbit primary antibodies, allowing for the detection and amplification of the target signal.

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2 protocols using hrp conjugated anti rabbit igg secondary antibody

1

Quantitative 5fC Detection in DNA

Check if the same lab product or an alternative is used in the 5 most similar protocols
Chemical labeling of 76mer model DNA containing single 5fC or Tdg−/− mESC gDNA was performed as described above. For the dot blot assay, different amounts of model DNA or gDNA were denatured in advance with NaOH solution (final concentration of 0.15M), spotted on the Amersham Hybond-N+ membrane (GE Healthcare) and air-dried for 5 min. The membrane was UV crosslinked and then blocked with 5% nonfat milk in 1x TBST at room temperature for 2 h. The membrane was then incubated with anti-5fC antiserum (Active Motif, 61223, 1:2,500 dilution) overnight at 4 °C followed by 1× TBST washing three times. After incubation with HRP-conjugated anti-rabbit IgG secondary antibody (CW Biotech, CW0103, 1:10,00 dilution) at room temperature for 1 h and washing with 1× TBST for three times, the membrane was supplied with 1 mL SuperSignal West Chemiluminescent Substrate (Thermo Scientific) and then visualized by chemiluminescence exposure.
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2

Quantitative 5fC Detection in DNA

Check if the same lab product or an alternative is used in the 5 most similar protocols
Chemical labeling of 76mer model DNA containing single 5fC or Tdg−/− mESC gDNA was performed as described above. For the dot blot assay, different amounts of model DNA or gDNA were denatured in advance with NaOH solution (final concentration of 0.15M), spotted on the Amersham Hybond-N+ membrane (GE Healthcare) and air-dried for 5 min. The membrane was UV crosslinked and then blocked with 5% nonfat milk in 1x TBST at room temperature for 2 h. The membrane was then incubated with anti-5fC antiserum (Active Motif, 61223, 1:2,500 dilution) overnight at 4 °C followed by 1× TBST washing three times. After incubation with HRP-conjugated anti-rabbit IgG secondary antibody (CW Biotech, CW0103, 1:10,00 dilution) at room temperature for 1 h and washing with 1× TBST for three times, the membrane was supplied with 1 mL SuperSignal West Chemiluminescent Substrate (Thermo Scientific) and then visualized by chemiluminescence exposure.
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