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According to optimal reaction factors, the antigenicity of all synthetic peptides was identified by analyzing the recognition and combination between peptides and standard antibody samples using the FP method.
All possible antigenic epitopes from hepatitis B virus (HBV) surface antigen protein were predicted, and the antigenicity of peptide was determined by analyzing the recognition and combination of peptide and standard antibody samples using the FP technique.
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Expression of Ki67 was assessed in Hong Kong tumor samples using the antibody SP6 (Neomarkers/LabVision), a rabbit monoclonal antibody, which provides similar accuracy, reproducibility and prognostic value when compared to MIB1 in primary breast cancer [ 24, 25].
Reflecting the US pattern, one German group analyzed 16 breast milk samples using the antibody-based test and reported finding glyphosate in all 16 samples (sorry--it's in German).
Anti- L. infantum IgG antibodies were found in 54/89 samples using the IFAT test, with titers ranging between 1 : 80 and 1 : 5120, and 51/89 samples were positive with the rapid immunochromatographic test.
We also stained 221 tumor samples using the same antibody.
Of these studies, the one on human solid tumors analyzed only 8 meningioma samples using the DAKO antibody we used in the present study but the staining protocol was not described in sufficient details [ 18].
HSV-2 specific antibody status was determined for serum samples using the HerpeSelect 2 ELISA IgG (Focus Diagnostics, Cypress, California, USA) according to the manufacturer's protocol [ 23] with the following exception.
Expression of the class I p85 adaptor and class II PI3K were assessed in 104 normal adult human samples using the above antibodies.
IHC was performed for these samples using the aforementioned AKR antibodies.
Whole cell lysate was isolated as described above and the proteins of interest were immunoprecipitated from an equivalent amount of protein for each sample using the specific antibodies.
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