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- 详细信息
- 文献和实验
- 技术资料
- 库存:
100
- 细胞类型:
科研
- 品系:
详情请咨询我司客服
- 组织来源:
详情请咨询我司客服
- 物种来源:
鼠/人/其它
- 细胞形态:
上皮样/成纤维样/其它
- 器官来源:
详情请咨询我司客服
- 运输方式:
常温运输/干冰运输
- 年限:
详情请咨询我司客服
- 生长状态:
贴壁/悬浮
- 英文名:
A549
产品简介:
[品系] ……………………Human
[组织来源]………………详情请咨询
[生长状态]………………贴壁/悬浮
[细胞类型]………………详情请咨询
[疾病] ……………………正常
[应用] ……………………科研
生物安全:
不含有 HIV-1、 HBV、HCV、支原体、细菌、酵母和真菌等。
产品包装:
提供新鲜或者冻存的细胞
使用方法:
如是新鲜细胞,客户收到细胞后应立即将其放入CO2细胞培养箱内静置3-4个小时,再进行后续的实验操作;如是冻存细胞, 客户收到细胞后应立即将其放入液氮、-80℃冰箱或立即进行复苏。
细胞培养 :
(1)Getting Started with an ATCC Cell Line:
ATCC cell lines and hybridomas are shipped frozen on dry ice in cryopreservation vials or as growing
cultures in flasks at ambient temperature. Upon receipt of frozen cells, it is important to immediately revive
them by thawing and removing the DMSO and placing them into culture. If this is not possible, store the
cells in liquid nitrogen vapor (below −130°C). Do not store frozen cells at temperatures above −130°C as
their viability will decline rapidly.
(2)细胞图片:

(3)Initiating Frozen Cultures:
1. Prepare a culture vessel so that it contains the recommended volume
of the appropriate culture medium as listed on the Product Sheet,
equilibrated for temperature and pH (CO₂).
2. Thaw the vial by gentle agitation in a water bath at 37°C or the normal growth temperature for that cell
line. Thawing should be rapid, approximately 2 minutes or until ice crystals have melted.
3. Remove the vial from the water bath and decontaminate it by dipping in or spraying with 70% ethanol.
Follow strict aseptic conditions in a laminar flow tissue culture hood for all further manipulations.
4. Unscrew the top of the vial and transfer the contents to a sterile
centrifuge tube containing 9 mL of the recommended medium.
Remove the cryoprotectant agent (DMSO) by gentle centrifugation (10
minutes at 125 × g). Discard the supernatant, and resuspend the cells
in 1 or 2 mL of complete growth medium. Transfer the cell suspension
into the culture vessel containing the complete growth medium and
mix thoroughly by gentle rocking.
Some ATCC cell, are shipped as growing cultures in culture vessels. These vessels are seeded with cells,
incubated to ensure cell growth and then filled completely with medium for shipping.
Upon receiving a flask culture, visually examine the medium for macroscopic evidence of microbial contamination. This includes
unusual pH shifts (yellow or purple color from the phenol red),
turbidity, or particles. With an inverted microscope at low power
(100×) check the medium for evidence of microbial contamination
as well as the morphology of the cells. See page 6 for more details
on examining cell cultures.
烜雅生物发布
质量可靠,售后有保障
如运输过程中导致细胞污染或者死亡,我们将无条件补发收货后十个工作日内有其他问题提供照片可半价重发
人肺腺癌细胞_A549相关产品:
| SHG-44 | 脑恶性胶质瘤细胞 |
| NEI-H209 | 小细胞肺癌细胞 |
| U251 | 神经胶质细胞瘤细胞 |
| NCI-H345 | 小细胞肺癌细胞 |
| M17 | 神经母细胞瘤细胞 |
| NCI-H446 | 小细胞肺癌细胞 |
| LAN-5 | 神经母细胞瘤细胞 |
| Bcap-37 | 乳腺髓样癌细胞 |
| LAN-6 | 神经母细胞瘤细胞 |
| BT474 | 乳腺导管瘤细胞 |
| SK-N-SH | 神经母细胞瘤细胞 |
| MDA-MB-157 | 乳腺癌细胞 |
| SH-SY5Y | 神经母细胞瘤细胞 |
| MDA-MB-231 | 乳腺导管癌细胞 |
| SF126 | 脑瘤细胞 |
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文献和实验导致无法捕获时间序列的变化,导致重要发现被忽略。 由于这些局限性,我们认为,直接和时间评估细胞增殖/细胞毒性的方法的发展对于使用培养细胞的研究领域是重要的。 试验大纲 为了验证 Evident Provi CM20 培养监测系统的细胞增殖/毒性评估能力,我们进行了以下两项检测,以将 CM20 系统与传统检测 (WST-8) 进行比较: 抗癌药物 (5-FU) 对人肺腺癌 A549 细胞的细胞死亡检测 神经毒素 (6-OHDA) 对人神经母细胞瘤 SH-SY5Y 细胞的细胞死亡检测
里程碑!张锋团队开发全新蛋白质递送系统,助力人类基因疗法和癌症治疗
Photorhabdus asymbiotica 产生的 eCIS 的尾部纤维,以靶向人类细胞。研究小组制造了靶向表达 EGFR 的癌细胞的 eCIS,并使用 A549 人肺腺癌细胞作为模型细胞系,用以测试改造后的 eCIS 是否可以靶向人类细胞。试验结果表明,改造后的 eCIS 杀死了几乎 100% 的表达 EGFR 的癌细胞,但不影响没有该受体的细胞。 图片来源:Nature 研究人员还调整了这一系统,使用 eCIS 将蛋白质输送到活小鼠的大脑,并且发现它不会引起可检测的免疫
人类组织肿瘤细胞 10104 人淋巴瘤细胞(B类)A-204 人横纹肌肉瘤A375 人皮肤黑色素瘤细胞A431 人皮肤基底细胞癌A549 人肺癌细胞A875 人黑色素瘤细胞BeWo 人胎盘绒毛癌细胞BGC-823 人胃腺癌细胞BT474 人乳腺导管瘤CACO-2 人结肠癌细胞CaLu-3 人肺腺癌细胞CASKI 人宫颈癌Colo205 人结肠癌Colo320DM 人结肠癌D341 Med 人髓母细胞瘤Daudi 人B淋巴细胞瘤DMF7 双位点HC-KIT
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