- 询价
- 进口
- 美国
- CSC-C2963
- 2025年07月13日
企业认证
- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
液氮保存
- 保质期：
永久
- 英文名：
CF2Th
- 库存：
1*10^6cells/vial
- 供应商：
美国
- 规格：
冻存管
风险提示：丁香通仅作为第三方平台，为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全，合理判断，谨慎选购商品，商家和用户对交易行为负责。对于医疗器械类产品，请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验Development of Conditionally Immortalized Epithelial Cell Lines from CF and Non-CF Mice
Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene are responsible for cystic fibrosis (CF) (1 ) and the primary defect in CF is the loss of cAMP-regulated anion conductance in the apical plasma membrane
Inflammatory Mediators in CF Patients
Patients with cystic fibrosis (CF) succumb to airway infection and inflammation, and determining the extent and nature of the infecting agents, as well as the extent and nature of the inflammatory response, is critical to understanding
Xenograft Model of the CF Airway
in associating cystic fibrosis (CF) defects with CFTR dysfunction, there are many unanswered questions concerning the roles of CFTR in both normal airway biology and in CF pathology. Before effective therapeutic approaches for CF lung disease will be realized
技术资料暂无技术资料 索取技术资料
