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Serum insulin was measured by radioimmunoassay using a polyclonal guinea pig antiserum (14).
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Here, we demonstrated that in third instar larvae, Cora was concentrated around the NMJ (Fig. 5A), using a polyclonal guinea-pig antibody directed against a sequence present only in large Cora isoforms [35].
Captured aflibercept was detected using a polyclonal anti-human IgG Fc antibody.
A polyclonal guinea pig antibody was raised against a peptide encompassing the sequence of the second C-terminal CRD domain (GCAPSCQQQCIPSCPRGCCGA) of Cnidoin (Eurogentec, Seraing, Liège, Belgium).
Following fixation, the cells were immunostained with a polyclonal guinea pig anti-chlamydia and mouse monoclonal anti-caveolin-2 antibodies as described above.
These assays used a polyclonal antibody against hCG dimer.
We used a polyclonal antibody against Laminin heterotrimer [34].
In some cases, doublestaining was performed for perilipin using a monospecific guinea pig polyclonal antibody (Progen, Heidelberg, Germany).
Insulin was measured by radioimmunoassay using polyclonal guinea pig antiserum at age 49 years and by double antibody enzyme-linked immunosorbant assay at age 61 years.
Nephrin was stained using a guinea pig (Acris, Germany) antibody with an anti-guinea pig TRITC labelled secondary (Jackson, Westgrove).
Normalization was performed via detection of actin levels using a mouse polyclonal antibody (Millipore, 1 2500).
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