1) colony forming efficiency
克隆形成率
1.
Effects of EGF and bFGF on colony forming efficiency of primary cultured rabbit corneal limbal stem cells;
EGF与bFGF单独及联合应用对原代培养的兔角膜缘干细胞克隆形成率的影响
2.
The output of viable cells,rates of adherence to dish,colony forming efficiency(CFE) of the isolated epidermal ce.
观察不同分离条件对表皮细胞生长情况、贴壁率、克隆形成率的影响。
3.
Limiting dilution assay was performed to determine the HL-60 cell colony forming efficiency (CPE).
方法应用电子显微镜、琼脂糖电泳、流式细胞术和ＴｄＴ介导的缺口和末端标记法（ＴＵＮＥＬ）等方法分析放射诱导ＨＬ－６０细胞凋亡，应用有限稀释法测定放射后细胞克隆形成率。
2) cloning efficiency
克隆形成率
1.
Objective:To determine the effects of ~(125)I radioactive seed on cloning efficiency of human esophageal carcinoma cell line Eca-109 in vitro.
目的:研究125I放射性粒子对体外培养的人食管癌Eca-109细胞克隆形成率的影响。
3) colony-forming efficiency
克隆形成率
1.
The resultant cells were observed and identified by cell growth curve,immnohistochemical staining and colony-forming efficiency.
采用组织块法从表皮和真皮中分离山羊皮肤干细胞,通过形态学观察、免疫组化染色以及克隆形成率等方法检测两种来源的皮肤干细胞体外生长特性。
2.
The resultant cells were cultured in vitro and identified by cell growth curve,immunohistochemical staining and colony-forming efficiency to compare the efficiency of the two methods for the cultivation and proliferation of hair follicle stem cells in vitro.
分别采用组织块法和酶消化法分离培养山羊毛囊干细胞,并通过形态学观察、免疫组化染色以及克隆形成率来比较2种方法体外分离培养毛囊干细胞的效率。
3.
The resultant cells were cultured in self-prepared serum-free conditional medium and studied through morphological observation,cell growth curve and colony-forming efficiency(CFE),and identified by immunohistochemical staining.
2 mg/mLEDTA)消化从山羊耳部皮肤分离得到毛囊干细胞,用自制无血清培养基培养,并用形态学观察、细胞生长曲线、克隆形成率及免疫组化染色检测,探讨毛囊干细胞体外分离培养方法及生物学特性。
4) colony-formation efficience
细胞克隆形成率
5) clone formation
克隆形成
1.
Methods We detect the multiplication, clone formation, DNA synthesis inhibitive rate and survival rate by liquid cultivation, clone formation, ~ 3 H-TdR addition and MTT colormrtric method.
方法通过液体培养法、克隆形成法、3H-TdR掺入法与MTT比色法分别检测给药后肺腺癌细胞的增殖情况、克隆形成率、DNA合成抑制率及生存率来探讨红景天的抑瘤效应。
2.
Clone formation assay,BrdU-labeled detain assay and SP cells detecting assay were carried out to analyze the TSCs in SP2/0 cells.
以克隆形成试验检测SP2/0细胞中具有形成克隆能力细胞的大体比例;采用BrdU标记滞留试验检测SP2/0细胞中含有DNA永生化链的细胞,即具有干细胞特性的细胞;检测SP2/0细胞中具有干细胞特性的SP细胞存在情况及其比例。
6) colony formation
克隆形成
1.
Effect of coixenolide on the colony formation of human nasopharyngeal carcinoma cell line CNE-2Z;
薏苡仁酯对人鼻咽癌细胞克隆形成的影响
2.
Cell colony formation in soft agar was observed as well.
6,克隆形成率为12。
3.
Furthermore,after hepatoma cells(Hep3B and HepG2) were treated with different concentrations of Andro(0-30 μmol·L-1) for 14 d,the number of colony formation was accounted under microscope.
实验中采用MTT法检测穿心莲内酯(0～50μmol·L·1)对L-02、Hep3B和HepG2细胞存活率的影响,通过软琼脂克隆形成实验检测穿心莲内酯(0～30μmol·L·1)与Hep3B和HepG2细胞孵育14d后对其克隆形成率的影响,通过流式细胞技术检测穿心莲内酯对Hep3B细胞周期的影响。
补充资料：集落形成率
分子式：
CAS号：
性质：在传代培养中，接种细胞形成集落的百分比。如果每个集落是由一个细胞形成的，这与克隆形成率同义。有时不严格地用于表示传代培养后生存细胞数，但这最好称为贴壁率(seeding efficiency)。
CAS号：
性质：在传代培养中，接种细胞形成集落的百分比。如果每个集落是由一个细胞形成的，这与克隆形成率同义。有时不严格地用于表示传代培养后生存细胞数，但这最好称为贴壁率(seeding efficiency)。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条