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Establishment by the rat lymph node method of epitope-defined monoclonal antibodies recognizing the six different ? chains of human type IV collagen

表位 单克隆抗体 分子生物学 淋巴结 抗体 抗原 化学 肽序列 氨基酸 免疫荧光 生物 生物化学 免疫学 基因
作者
Yoshikazu Sado,Megumi Kagawa,Yumiko Kishiro,Katsuyuki Sugihara,Ichiro Naito,Jerome M. Seyer,Manabu Sugimoto,Toshitaka Oohashi,Yoshifumi Ninomiya
出处
期刊:Histochemistry and Cell Biology [Springer Science+Business Media]
卷期号:104 (4): 267-275 被引量:206
标识
DOI:10.1007/bf01464322
摘要

A group of rat monoclonal antibodies recognizing the six different α chains of human type IV collagen have been established by our novel method. The method is designated the rat lymph node method in which enlarged medial iliac lymph nodes of a rat injected with an antigen emulsion via hind footpads are used as a source of B cells for cell fusion to produce hybridomas. The immunogens used were synthetic peptides having non-consensus amino acid sequences near the carboxyl termini of type IV collagen α chains. Hybridomas were screened both by ELISA with synthetic peptides and by indirect immunofluorescence with cryostat sections of human kidneys. Because the epitopes of all antibodies were determined by multipin-peptide scanning, they were confirmed to be isoform-specific. They are useful for identification of α chains of type IV collagen at the protein level in normal and abnormal conditions. The combined use of synthetic peptides as immunogens, the rat lymph node method as making monoclonal antibodies, and the multipin-peptide scanning as epitope mapping is found to be a strong tool for identification of peptides and proteins whose amino acid sequences are known or have been deduced.
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