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- R&D
- 美国
- 2695-SE-010
- 2025年11月12日
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- 详细信息
- 文献和实验
- 技术资料
- 保质期：
见产品批号
- 英文名：
Recombinant Human Airway Trypsin-like Protease/HAT, CF (10 ug)
- 库存：
需确认
- 供应商：
嵘崴达
- CAS号：
见说明书
- 保存条件：
见说明书
- 规格：
10 UG
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| 2695-SE-010 | Recombinant Human Airway Trypsin-like Protease/HAT, CF (10 ug) |
| 2696-PG-050 | Recombinant Mouse PGLYRP1/PGRP-S Protein (50 ug) |
| 2696-PG-050/CF | Recombinant Mouse PGLYRP1/PGRP-S Protein, CF (50 ug) |
| 2706-CL-01M/CF | Recombinant Human CD40 Ligand/TNFSF5 (Histidine-tagged), CF (1 MG) |
| 2706-CL-025 | Recombinant Human CD40 Ligand/TNFSF5 (Histidine-tagged) (25 ug) |
| 2706-CL-025/CF | Recombinant Human CD40 Ligand/TNFSF5 (Histidine-tagged), CF (25 ug) |
| 2706-CL-500/CF | Recombinant Human CD40 Ligand/TNFSF5 (Histidine-tagged), CF (500 UG) |
| 2707-RM-025 | Recombinant Rhesus Macaque IL-5 Protein (25 ug) |
| 2707-RM-025/CF | Recombinant Rhesus Macaque IL-5 Protein, CF (25 ug) |
| 2708-MS-050 | Recombinant Human SR-AI/MSR Protein, CF (50 ug) |
| 2709-NP-025 | Recombinant Mouse Neuropoietin Protein (25 ug) |
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文献和实验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
Development of Conditionally Immortalized Epithelial Cell Lines from CF and Non-CF Mice
84) cells or heterologous expression systems (4 -9 ). Epithelial cells from other tissues affected by cystic fibrosis have received relatively little attention, primarily due to the lack of access to appropriate human material. The development of the CF
Cystic fibrosis (CF) is a common inherited disorder affecting a variety of epithelial tissues. The disease is caused by mutations in the cystic fibrosis transmembrane conductance regulator gene (CFTR) that lead to abnormal secretions
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