| Notes | |
|---|---|
| Storage Buffer | 0.25%胰蛋白酶 |
| Similar Names | |
| Clone Number | |
| Isotype | |
| Positive Control | |
| Chemical Name | Endothelial Progenitor Cells from Rat Peripheral Blood |
| Remark | |
| Storage Instructions | 气相:空气,95%;CO2,5% |
| Cell Name | Endothelial Progenitor Cells from Rat Peripheral Blood |
| Growth Medium | 含FBS、生长添加剂、Penicillin、Streptomycin |
|---|---|
| Species Reactivity | |
| Growth | 贴壁 |
| Antigen Exp | |
| Applications | |
| Conjugation | |
| Clone | |
| Storage Condition | |
| Gene Exp | |
| Doubling Time | |
| Receptor Exp | |
| Immunogen | |
| Host Species | |
| Generation Ratio | 可传1-2代;不建议多次传代 |
| Characters | 内皮细胞样 |
| Culture Conditions | |
|---|---|
| BSL | |
| Notes | |
| Liquid Frequency |
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在现代医学和生物技术迅猛发展背景下,mRNA疫苗技术的兴起,不仅标志着疫苗研发进入了一个新时代,也为传染病预防和治疗提供了全新的思路和方法。mRNA疫苗,作为一种基于核酸的疫苗,与DNA疫苗相比,具有不整合至宿主基因组的显著优势,降低了基因突变风险。此外,与已被广泛使用的蛋白质疫苗相比,mRNA疫苗的无细胞生产方式不仅加快了疫苗的研发周期,还提高了生产效率和规模化生产的可能性。mRNA疫苗能编码多种抗原,适应多样化的微生物或病毒变体,同时结合编码抗原和佐剂的双重功能,有效激发免疫反应。
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