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- 595-P4-025
- 2025年11月25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 Mouse CXCL4/PF4, CF
- 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：
25 UG
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MCE激动剂，ACROS、ALFA、阿拉丁等生化试剂现货定购。
| 595-P4-025 | Recombinant Mouse CXCL4/PF4 Protein, CF (25 ug) |
| 5964-GT-020 | Recombinant Human Fucosyltransferase 11/FUT11 Protein, CF (20 ug) |
| 5967-ST-010 | Recombinant Human NDST1 Protein, CF (10 ug) |
| 5968-ST-020 | Recombinant Human HS3ST1 Protein, CF (20 ug) |
| 5969-GH-010 | Recombinant Human Cytosolic beta-Glucosidase/GBA3, CF (10 ug) |
| 596-MR-100 | Recombinant Mouse IL-21R Fc Chimera Protein, CF (100 ug) |
| 597-LM-010 | Recombinant Mouse Limitin/IFN-zeta Fc Chimera Protein, CF (10 ug) |
| 5987-BD-050 | Recombinant Mouse beta-Defensin 3 Protein, CF (50 ug) |
| 5988-FZ-050 | Recombinant Human Frizzled-1 Fc Chimera Protein, CF (50 ug) |
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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
Design of Gene Therapy Clinical Trials in CF Patients
On April 17, 1993, Crystal and co-workers initiated the first human gene therapy trial for cystic fibrosis (CF). In that study, a replication-deficient recombinant adenovirus encoding cystic fibrosis transmembrane conductance regulator (CFTR
Recombinant Antigens in Viral Diagnosis
(CF) assays (2 ). Although these assays can be specific and reliable in the hands of an experienced laboratory worker, they suffer from several significant disadvantages. HI and CF assays are frequently very specific, but are relatively insensitive
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