中国医疗前沿2013,Issue(23) :29-30.DOI:10.3969/j.issn.1673-5552.2013.23.0016

APCmin/+;Mac-1-/-小鼠模型的构建

Establishment of APCmin/+;Mac-1-/- mice model

雷岩 章倩倩 胡曦文 刘红英 郑凌云 顾取良 何晓东 王丽京
中国医疗前沿2013,Issue(23) :29-30.DOI:10.3969/j.issn.1673-5552.2013.23.0016

APCmin/+;Mac-1-/-小鼠模型的构建

Establishment of APCmin/+;Mac-1-/- mice model

雷岩 1章倩倩 1胡曦文 1刘红英 1郑凌云 2顾取良 2何晓东 1王丽京1
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作者信息

  • 1. 510006 广州,广东药学院血管生物学研究所
  • 2. 广东药学院基础学院
  • 折叠

摘要

目的:构建APCmin/+;Mac-1-/-小鼠模型。方法将自发肠腺瘤(APCmin/+)模型同β2家族整合素Mac-1缺失的小鼠(Mac-1-/-)进行杂交,剪小鼠尾巴抽提DNA,然后用PCR法鉴定小鼠的基因型。结果将APCmin/+小鼠与Mac-1-/-小鼠杂交3代后,成功构建了APCmin/+;Mac-1-/-小鼠模型。结论将APCmin/+小鼠与Mac-1-/-小鼠杂交3代后成功建立了APCmin/+;Mac-1-/-小鼠模型,进一步扩大种群。

Abstract

Objective To establish the APCmin/+;Mac-1-/- mice. Methods Female PSGL-1 KO mice were mated with male APCmin/+ mice and male progeny carrying the APCmin/+ transgene. Mice were genotyped by PCR. Results After female Mac-1 KO mice were mated with male APCmin/+ mice for three generations, APCmin/+;Mac-1-/- mice were established. Conclusion APCmin/+;Mac-1-/- mice were obtained and propagated through APCmin/+ mice being mated with MAC-1 KO mice.

关键词

结直肠肿瘤/β2整合素/MAC-1/动物模型

Key words

Intestinal tumor/β2 integrin/MAC-1/Animal model

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基金项目

出版年

2013
中国医疗前沿
中国医院协会

中国医疗前沿

影响因子:0.186
ISSN:1673-5552
参考文献量9
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