上海雅吉生物科技有限公司
首页 产品目录 产品目录(简版) 公司动态 企业认证 公司相册 联系我们

文献引用产品|小鼠单克隆抗体亚型鉴定(MAI)Elisa试剂盒

发布人:上海雅吉生物科技有限公司

发布日期:2026/5/12 8:53:53

文章标题:Preparation and Biochemical Characteristics of a New IgG-Type Monoclonal Antibody against K Subgroup Avian Leukosis Virus

影响因子:4.132
期刊:ACS Omega
作者列表:Xiaochen Zhang, Hongmei Li, Chengcheng Wang, Yixuan Du, Yuying Li, Liwei Zhang, Mengjie Huang, Jianhua Qiu, Huijun Guo
发表时间:2022-12-22
DOI:10.1038/s41598-025-97643-7
主要研究成果:Abstract
This study focused on preparing a new IgG-type monoclonal antibody (MAb) against subgroup K avian leukosis virus (ALV-K) and identifying its biochemical characteristics. A specific gene fragment of ALV-K was amplified by polymerase chain reaction and expressed in E. coli. The purified expressed products were inoculated into BALB/c mice to prepare antibody-secreting spleen lymphocytes, and hybridoma cells were obtained after cell fusion of spleen lymphocytes and myeloma cells. A new hybridoma cell line named 30B9, which stably secreted IgG2b-antibody against ALV-K, was screened and contained 98 chromosomes. The MAb secreted by the 30B9 cells could recognize the ALV-K strain but not the ALV-A/B/J strains in an indirect immunofluorescence assay. Seventeen overlapping truncated ALV-K gp85 protein fragments were expressed, and eight peptides were artificially synthesized to analyze the MAb’s antigen epitope by Western blot or enzyme-linked immunosorbent assay, and the results showed that the linear epitope was located on the 217–RRNYT–221 of ALV-K gp85 protein. A bioinformatics analysis showed that the epitope has a high antigenicity index, hydrophilicity, and surface accessibility and forms a unique linear spatial structure. Its five amino acids are highly conserved in all published ALV-K strains but are very low in ALV-A/B/J/C/D/E strains. This study provides a new biomaterial for developing specific detection methods against ALV-K.


相关新闻资讯

qPCR实验检测不到Ct值的原因

2026/05/13

根据搜索结果,qPCR实验检测不到Ct值可能有以下原因一、模板相关问题模板量不足或降解样本中目标基因含量过低或不存在表达cDNA或DNA模板在制备过程中发生降解解决:增加模板上样量,从系列稀释样本的高浓度端开始模板中存在抑制剂残留的乙醇、SDS、酚等物质抑制Taq酶活性解决:纯化模板(柱式纯化或乙醇沉淀)或稀释cDNA(1:5或1:10)模板质量问题RNA或逆转录cDNA部分降解导致无法扩增二、引

文献引用产品|NHA人星形胶质细胞

2026/05/12

  文章标题:LINC00665 functions as a competitive endogenous RNA to regulate AGTR1 expression by sponging miR‑34a‑5p in glioma影响因子:3.906期刊:ONCOLOGY REPORTS作者列表:Yongyue Dai, Yucheng Zhang, Maolin Hao, Renwu

文献引用产品|人胚肾细胞293T/17

2026/05/12

 文章标题:LINC00665 functions as a competitive endogenous RNA to regulate AGTR1 expression by sponging miR‑34a‑5p in glioma影响因子:3.906期刊:ONCOLOGY REPORTS作者列表:Yongyue Dai, Yucheng Zhang, Maolin Hao, Renwu Z