• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Establishment of monoclonal antibodies against human erythrocyte NADH-cytochrome b5 reductase.

作者信息

Lan F, Tang Y, Huang C, Zhu Z

机构信息

Center of Clinical Laboratory Diagnostics, Donfang Hospital, Fujian Province, China.

出版信息

Hybridoma. 1996 Aug;15(4):295-8. doi: 10.1089/hyb.1996.15.295.

DOI:10.1089/hyb.1996.15.295
PMID:8880217
Abstract

NADH-cytochrome b5 reductase (b5R) is a multifunctional redox enzyme, whose deficiency leads to hereditary methemoglobinemia. By using recombinant human red cell b5R as antigen to immunize BALB/c mice and conventional cell fusion, we have established two mouse hybridoma cell lines secreting IgG monoclonal antibodies (MAbs) to b5R. In immunoblotting, the MAbs were shown to react specifically with b5R. They were also found to be capable of capturing b5R activity from b5R solution and normal human hemolysate. It was implied that the binding sites of the MAbs might not be proximal to the active site of the enzyme, but might be in close proximity to each other. The MAbs will be useful in b5R-related investigations.

摘要

相似文献

1
Establishment of monoclonal antibodies against human erythrocyte NADH-cytochrome b5 reductase.
Hybridoma. 1996 Aug;15(4):295-8. doi: 10.1089/hyb.1996.15.295.
2
Antibody-based spot test for NADH-cytochrome b5 reductase activity for the laboratory diagnosis of congenital methemoglobinemia.用于先天性高铁血红蛋白血症实验室诊断的基于抗体的NADH-细胞色素b5还原酶活性斑点试验。
Clin Chim Acta. 1998 May 8;273(1):13-20. doi: 10.1016/s0009-8981(98)00022-9.
3
Determination of concentration of cytosolic NADH-cytochrome b5 reductase in erythrocytes from normal Chinese adults, neonates and patients with hereditary methemoglobinemia by double-antibody sandwich ELISA.采用双抗体夹心酶联免疫吸附测定法测定正常中国成年人、新生儿及遗传性高铁血红蛋白血症患者红细胞中胞质NADH-细胞色素b5还原酶的浓度。
Acta Haematol. 1998;100(1):44-8. doi: 10.1159/000040862.
4
Serine-proline replacement at residue 127 of NADH-cytochrome b5 reductase causes hereditary methemoglobinemia, generalized type.NADH-细胞色素b5还原酶第127位残基的丝氨酸-脯氨酸置换导致遗传性高铁血红蛋白血症,全身性类型。
Blood. 1990 Apr 1;75(7):1408-13.
5
[Leu 72 Pro mutation in the NADH-cytochrome b5 reductase gene found in a Chinese hereditary methemoglobinemia patient].
Zhonghua Xue Ye Xue Za Zhi. 1998 Apr;19(4):195-7.
6
Identification of a cytochrome b-type NAD(P)H oxidoreductase ubiquitously expressed in human cells.一种在人类细胞中普遍表达的细胞色素b型NAD(P)H氧化还原酶的鉴定。
Proc Natl Acad Sci U S A. 1999 Dec 21;96(26):14742-7. doi: 10.1073/pnas.96.26.14742.
7
Concentration of NADH-cytochrome b5 reductase in erythrocytes of normal and methemoglobinemic individuals measured with a quantitative radioimmunoblotting assay.用定量放射免疫印迹分析法测定正常人和高铁血红蛋白血症患者红细胞中NADH-细胞色素b5还原酶的浓度。
J Clin Invest. 1987 Nov;80(5):1296-302. doi: 10.1172/JCI113205.
8
[Molecular analysis of the structure of the mutant NADH-cytochrome b5 reductase gene causing methemoglobinemia].[导致高铁血红蛋白血症的突变型NADH-细胞色素b5还原酶基因结构的分子分析]
Fukuoka Igaku Zasshi. 1990 Jan;81(1):41-7.
9
A novel mutation in the NADH-cytochrome b5 reductase gene of a Chinese patient with recessive congenital methemoglobinemia.一名患有隐性先天性高铁血红蛋白血症的中国患者的NADH-细胞色素b5还原酶基因中的新突变。
Blood. 2000 May 15;95(10):3250-5.
10
Membrane-bound cytochrome b5 reductase (methemoglobin reductase) in human erythrocytes. Study in normal and methemoglobinemic subjects.人红细胞中的膜结合细胞色素b5还原酶(高铁血红蛋白还原酶)。对正常人和高铁血红蛋白血症患者的研究。
J Clin Invest. 1981 Jan;67(1):149-55. doi: 10.1172/JCI110007.