相关产品推荐更多 >
万千商家帮你免费找货
0 人在求购买到急需产品
- 详细信息
- 询价记录
- 文献和实验
- 技术资料
- 英文名:
H358; H-358; NCIH358
- 库存:
复苏:1-2周。冻存:现货。(建议:复苏为主,极个别特殊情况选冻存)
- 供应商:
上海富衡生物科技有限公司
- 肿瘤类型:
肺腺癌(肺癌)
- 细胞类型:
真核细胞
- 品系:
人源肺腺癌细胞系
- 组织来源:
肺腺癌肿瘤
- 相关疾病:
肺腺癌(KRAS 突变型)
- 物种来源:
人源
- 免疫类型:
非免疫细胞
- 细胞形态:
上皮样
- 是否是肿瘤细胞:
是
- 器官来源:
肺
- 运输方式:
常温/干冰,快递运输
- 年限:
数年
- 生长状态:
贴壁生长
- 规格:
1 × 10⁶ cells/T25 flask/冻存管
| 规格: | 1 × 10⁶ cells/T25 flask | 产品价格: | ¥1200.0 |
|---|---|---|---|
| 规格: | 冻存管 | 产品价格: | ¥1500.0 |
NCI-H358 细胞系是一种人非小细胞肺癌(NSCLC)细胞系,其组织来源为人类肺腺癌(Adenocarcinoma of the Lung)肿瘤组织。该细胞系由美国国家癌症研究所(National Cancer Institute, NCI)建立,常用于非小细胞肺癌的基础研究、靶向药物开发及肿瘤微环境机制探讨。
| 产品名称 | 人非小细胞肺癌细胞;NCI-H358(STR) |
|---|---|
| 品牌 | FuHeng |
| 英文名 | NCI-H358 |
| 货号 | FH0046 |
| 规格 | 1 × 10⁶ cells/T25 flask |
| 培养 | RPMI 1640 + 10% FBS + 1% P/S |
| 别称 | H358; H-358; NCIH358 |
| 形态特征 | 上皮样 |
| 生长特性 | 贴壁生长 |
| 培养基 | NCI-H358完全培养基 |
| 培养条件 | 气相:95% 空气,5% CO₂;温度:37 ℃ |
| 传代方法 | 1:2。3天内可长满。 |
| 组织来源 | 肺腺癌肿瘤 |
| 产品分类 | 人源细胞系 |
| 特别声明 | 富衡细胞库承诺尽最大努力对实验细胞资源相关信息进行及时更新。但限于当时的技术条件,细胞库资料不保证其准确性。 |
风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。
- 作者
- 内容
- 询问日期
文献和实验| 论文标题 | DOI | 发表时间 | 期刊 | 影响因子 | 作者列表 |
| ZEB1 Contributes to Drug Resistance Through Canonical Wnt Signaling in Lung Cancer | 10.1002/iub.70053 | 2025-08-12 | IUBMB LIFE | 3.2 | Hubo Shi, Min Wang, Qianqian Zhao, Yihui Xu |
| Ticagrelor inhibits the growth of lung adenocarcinoma by downregulating SYK expression and modulating the PI3K/AKT pathway | 10.1038/s41598-025-02721-5 | 2025-05-20 | Scientific Reports | 3.9 | Song Yuanhong, He Suwei, Zeng Lanhui, He Yuanqiao, Huang Ling |
| LPCAT3 is transcriptionally regulated by YAP/ZEB/EP300 and collaborates with ACSL4 and YAP to determine ferroptosis sensitivity | 10.1089/ars.2023.0237 | 2023-05-11 | ANTIOXIDANTS & REDOX SIGNALING | 6.6 | Mr. Jiangtao Cui, Dr. Yikun Wang, Ms. Xiaoting Tian, Ms. Yayou Miao, Prof. Lifang Ma, Ms. Congcong Zhang, Dr. Xin Xu, Dr. Jiayi Wang, Prof. Wentao Fang, Prof. Xiao Zhang |
| Essential roles of exosome and circRNA_101093 on ferroptosis desensitization in lung adenocarcinoma | 10.1002/cac2.12275 | 2022-02-20 | Cancer Communications | 15.3 | Xiao Zhang, Yunhua Xu, Lifang Ma, Keke Yu, Yongjie Niu, Xin Xu, Yi Shi, Susu Guo, Xiangfei Xue, Yikun Wang, Shiyu Qiu, Jiangtao Cui, Hong Wang, Xiaoting Tian, Yayou Miao, Fanyu Meng, Yongxia Qiao, Yongchun Yu, Jiayi Wang |
| Transcriptional Repression of Ferritin Light Chain Increases Ferroptosis Sensitivity in Lung Adenocarcinoma | 10.3389/fcell.2021.719187 | 2021-10-26 | Frontiers in Cell and Developmental Biology | 6.7 | Wang Yikun, Qiu Shiyu, Wang Hong, Cui Jiangtao, Tian Xiaoting, Miao Yayou, Zhang Congcong, Cao Leiqun, Ma Lifang, Xu Xin, Qiao Yongxia, Zhang Xiao |
| CREB stimulates GPX4 transcription to inhibit ferroptosis in lung adenocarcinoma | 10.3892/or.2021.8039 | 2021-04-02 | ONCOLOGY REPORTS | 3.9 | Zhixian Wang, Xiao Zhang, Xiaoting Tian, Yueyue Yang, Lifang Ma, Jiayi Wang, Yongchun Yu |
| Endogenous glutamate determines ferroptosis sensitivity via ADCY10-dependent YAP suppression in lung adenocarcinoma | 10.7150/thno.55482 | 2021-03-24 | Theranostics | 11.6 | Xiao Zhang, Keke Yu, Lifang Ma, Zijun Qian, Xiaoting Tian, Yayou Miao, Yongjie Niu, Xin Xu, Susu Guo, Yueyue Yang, Zhixian Wang, Xiangfei Xue, Chuanjia Gu, Wentao Fang, Jiayuan Sun, Yongchun Yu, Jiayi Wang |
polymorphic Y chromosome-specific short tandem repeats (STRs) have been described and a set of 9 loci were selected, considered as the minimal haplotype included in the forensic databases, Y-STR Haplotype Reference Databases, the largest now available online
Constructing STR Multiplex Assays
Multiplex polymerase chain reaction (PCR) refers to the simultaneous amplification of multiple regions of deoxyribonucleic acid (DNA) using PCR. Commercial short tandem repeat (STR) assays that can coamplify as many as 16 different loci
都是贴壁细胞,在消化传代过程中,步骤如下:倒尽旧的培养液->用无血清的培养基清洗一两次->加入一定量的胰酶,置于37度培养箱中5--10分钟,使细胞悬浮->显微镜下观察,待细胞大部分变圆时,回到超静台->加入一定量的含血清的新培养液,以终止胰酶作用->反复吹打细胞->再置显微镜下观察,直到细胞全部悬浮起来->吸出一部分加入新的培养瓶中->最后再补充加入一定量新的培养液。注意: 1、吹细胞时尽量多吹边角儿,此处细胞生长的多。2、吸出细胞前要混匀,可以剧烈震荡培养瓶。3、我们用的是DMEM











