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- 详细信息
- 文献和实验
- 技术资料
- 物种来源:
人
- 是否是肿瘤细胞:
0
- 细胞类型:
成纤维细胞
- 年限:
20 years
- 生长状态:
贴壁生长
- 相关疾病:
正常
- ATCC Number:
CCL-211™
- 细胞形态:
成纤维样
- 运输方式:
冻存运输
- 器官来源:
肺
- 库存:
大量
| Designations: | Hs888Lu | ||
| Depositors: | WA Nelson-Rees | ||
| Biosafety Level: | 1 | ||
| Shipped: | frozen | ||
| Medium & Serum: | See Propagation | ||
| Growth Properties: | adherent | ||
| Organism: | Homo sapiens | ||
| Morphology: | fibroblast |
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| Source: | Organ: lung Disease: normal Cell Type: fibroblast |
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| Permits/Forms: | In addition to the MTA mentioned above, other ATCC and/or regulatory permits may be required for the transfer of this ATCC material. Anyone purchasing ATCC material is ultimately responsible for obtaining the permits. Please click here for information regarding the specific requirements for shipment to your location. | ||
| Isolation: | Isolation date: August, 1975 | ||
| DNA Profile (STR): | Amelogenin: X,Y CSF1PO: 10,11 D13S317: 11,14 D16S539: 8,12 D5S818: 13 D7S820: 7,11 THO1: 10,9.3 TPOX: 8,11 vWA: 15,18 |
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| Cytogenetic Analysis: | normal male; diploid; stable | ||
| Age: | 20 years | ||
| Gender: | male | ||
| Ethnicity: | Caucasian | ||
| Comments: | The line was derived from normal tissue from patient who had osteosarcoma metastatic to the lung. The tissue was taken from a normal area of lung. |
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| Propagation: | ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Dulbecco's Modified Eagle's Medium, Catalog No. 30-2002. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%. Temperature: 37.0°C Atmosphere: air, 95%; carbon dioxide (CO2), 5% |
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| Subculturing: | Protocol:
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| Preservation: | Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO Storage temperature: liquid nitrogen vapor phase |
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| Related Products: | normal (or near-normal) cell line established from the same patient:ATCC CRL-7622 | ||
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文献和实验K4me3 信号,发现 CUT&Tag 信号在分辨率和灵敏度上均优于 ChIP-Seq 信号。 图 5. CUT&Tag 与 ChIP-Seq IGV 视图比较【3】 该研究成果为进一步研究植物中的表观基因组学提供了一个有前途的策略。在操作简单性和所需的时间方面,CUT&Tag 优于传统染色质分析方法。更重要的是 CUT&Tag 需要更少的起始材料,更少的测序数据得到更高质量的数据。 参考文献: 【1】 Kaya-Okur HS, Wu SJ
Bioresource Technology | 利用宏基因组,中山大学首次阐释微生物除磷的转化机制
500 mg/L 的硫酸盐。在厌氧 - 缺氧条件下,硫酸盐可被还原为有毒的、具有腐蚀性并且带恶臭的硫化氢 (H2S 和 HS−),从而破坏废水运输系统,抑制污水传统生物除磷 (CEBPR) 处理中的微生物反应过程。这个问题在在很长的一段时间内都没有得到妥善解决,直到 Rubio-Rincon 等人在 2017 年发现,在传统的生物除磷系统中加入硫代谢微生物如 Thiothrix caldifontis 可以实现富硫酸盐废水中的磷的高效生物去除。他们使用的是一种新型厌氧 / 缺氧反硝化硫循环强化
-888 镊子P-888 HOZAN-0066 镊子P-887 镊子P-887 HOZAN-0090 镊子头P-816R-1 镊子头P-816R-1 HOZAN-0104 吸盘P-832-L 吸盘P-832-L HOZAN-0068 青铜镊子P-893 青铜镊子P-893 HOZAN-0077 防静电镊子P-814-S 防静电镊子P-814-S HOZAN-0058 压接钳P-706 压接钳P-706 HOZAN-0011 剪钳N-21 剪钳N-21 HOZAN
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