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- 文献和实验
- 技术资料
- 英文名:
/
- 库存:
现货库存
- 供应商:
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- 肿瘤类型:
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- 细胞类型:
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- 品系:
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- 组织来源:
ATCC/DSMZ/ECACC
- 相关疾病:
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- 物种来源:
人或动物
- 免疫类型:
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- 细胞形态:
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- 是否是肿瘤细胞:
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- 器官来源:
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- 运输方式:
常温或干冰
- 年限:
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- 生长状态:
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- 规格:
T25
| 种属 | 人 |
| 组织来源 | 头皮组织 |
| 传代比例 | 1:2传代 |
| 完全培养基配置 | 基础培养基500ml ;生长添加剂5ml ;双抗5ml |
| 简介 | 毛囊是包围在毛发根部的囊状组织 ,内层是上皮组织性毛囊 ,外层是结缔组织性毛囊 ,内层与表皮相连 ,外层则与真 皮相连 ,毛囊作为一种重要的皮肤附属器官 ,最为显著的特点是始终处于生长期、退行期和休止期的周期性循环中。 在毛囊的形态学和周期性循环中 ,毛囊的角质细胞作为一种特殊类型的角质形成细胞 ,受毛乳头细胞分泌的一些细胞 因子或信号因子等作用 ,迅速发生分化增殖或凋亡 ,进而诱导毛囊进入生长期或退行期。 |
| 形态 | 上皮样细胞样 |
| 生长特征 | 贴壁生长 |
| 细胞检测 | 广谱角蛋白((PCK)免疫荧光染色为阳性疫荧光鉴定 ,细胞纯度可达90%以上 ,不含有HIV-1、HBV、HCV、支原 体、细菌、酵母和真菌等。 |
The present study investigated the applicability of a muscle volume prediction method using only the muscle length (L(M)), the maximum anatomical cross-sectional area (ACSA(max)), and a muscle-specific shape factor (p) on the quadriceps vastii. L(M), ACSA(max), muscle volume, and p were obtained from magnetic resonance images of the vastus intermedius (VI), lateralis (VL), and medialis (VM) of female (n = 20) and male (n = 17) volleyball athletes. The average p was used to predict muscle volumes (V(p)) using the equation V(p) = p × ACSA(max) × L(M). Although there were significant differences in the muscle dimensions between
Results: Activated immune cells such as macrophages M1, dendritic cells (DCs), innate lymphoid cells (ILC2), NK cells, Th1, follicular T helper cells (TFH), TCD8+, B lymphocytes and eosinophils have inhibitory eklects on tumourigenesis, while tolerogenic cells such as macrophages M2, tolerogenic DCs, ILC3, T and B regulatory lymphocytes appear to
through the development of immune checkpoint inhibitors. Already approved by the U.S. Food and Drug Administration for advanced melanoma and non-small cell lung cancer, immune
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文献和实验/Results: Activated immune cells such as macrophages M1, dendritic cells (DCs), innate lymphoid cells (ILC2), NK cells, Th1, follicular T helper cells (TFH), TCD8+, B lymphocytes and eosinophils have inhibitory eklects on tumourigenesis, while tolerogenic cells such as macrophages M2, tolerogenic DCs, ILC3, T and B regulatory lymphocytes appear to
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