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Titlebook: Breast Cancer Immunodiagnosis and Immunotherapy; Roberto L. Ceriani Book 1989 Springer Science+Business Media New York 1989 antibody.antig

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Jamin V. Brahmbhatt MD,Sijo J. Parekattil MD the cDNA was isolated from a genomic library and encompasses 7.5 kb. A 2.3 kb segment of this gene was found to be an array of tandem 60 bp repeat units whilst the remaining parts of the gene do not contain these repeats. The fact that these non-repeat sequences hybridize to identical mRNA species,
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The Potential of Synthetic Tumor-Associated Glycoconjugates (S-TAGs) for Generating Monoclonal Antibaled on normal human erythrocytes by neuraminidase treatment, TF has been characterized as: β-D-Gal-(1–3)- α-GalNAc, attached to glycophorin or other glycoproteins through O-serine or O-threonine linkages (1). Tn, the TF precursor, is reported to be α-GalNAc-O-serine/ threonine. While TF is normally
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Extracellular Keratins: An Updatet cancer cell lines (1). One of the antibodies, UCD/PR 10.11, has proven to be an excellent reagent, when used in the immunoperoxidase technique, for the diagnosis of epithelial malignancies (2). UCD/PR 10.11 reacts with CK 8 and 18. It has a superb signal-to-noise ratio in staining almost all simpl
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Preclinical Evaluation of MoAbs Mc5 and BrElare shared with other epithelial tissues of the body. In addition, neoplastic breast epithelial cells possess certain epitopes on their glycoproteins that could be oncofetal in nature and are considered tumor specific by others. They are epitopes that are made more available as a result of a lack of
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Clinical and Molecular Investigations of the DF3 Breast Cancer-Associated Antigen(1). Immunoperoxidase studies have demonstrated that MAb DF3 clearly distinguishes malignant and benign breast lesions. Whereas MAb DF3 produces a cytosolic staining pattern in 78% of breast carcinomas, such a pattern is observed in less than 10% of fibrocystic lesions or fibroadenomas (1). In contr
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