计算溶液所需的质量、体积或浓度。
BioReagent,即用型,无菌过滤,用于细胞培养,通过内毒素测试 级 ,适用于对基线干扰要求严格的色谱和分析工作流程。
-20°C储存。超低温运输 。请查阅批次 COA 获取详细规格。
SDS、COA、产品数据表及规格说明书均可下载。可通过批号查询获取批次 COA。
在色谱分析、有机合成和交叉偶联反应领域已被 0 篇同行评审文献引用。
是否无菌:是
本产品是一种即用型的培养细胞低温冻存液,已经过无菌处理,待冻存的细胞收集后,加入适量冻存液混匀即可,无需自行配制任何溶液,使用非常便捷,适用于绝大部分的哺乳动物细胞冻存。
产品特点
1、高品质——细胞复苏率在90%以上;
2、使用方便——2~8℃即可稳定保存,无需冷冻,即取即用。
使用说明
细胞冻存步骤
1、收集处于对数生长期贴壁细胞或悬浮细胞于离心管中,并进行细胞计数;
2、取所需冻存细胞数的细胞悬浮液置于离心管中,离心收集细胞(参考离心条件:1,000~2,000rpm,3~5min)。彻底移去离心管中的上清液;
3、加入适量的细胞冻存液于离心管中,调整细胞浓度至1~5×106cells/mL。轻柔混匀,制成细胞冻存悬液;
4、将离心管中的细胞冻存悬液分装于已标示完全的冻存管中;
5、将细胞冻存管放置于可逐步降低温度的装置(如程序降温盒)内并存入-80℃冰箱,确保冷却速度约为1℃/min。通常冷却速度不宜快于0.5℃/min;
6、若需液氮保存,需放-80℃冰箱过夜后移至液氮罐。
细胞复苏步骤
1、取出冻存的细胞,立即放入37℃水浴槽中快速解冻;
2、待冻存管中细胞混合液完全融化后,立即移入含5mL细胞培养基的离心管中,离心收集细胞(参考离心条件:1,000~2,000rpm,3~5min);
3、小心移去上清液。加入适量的新鲜细胞培养基,轻轻混匀,将细胞混合液移至事先准备好的培养容器中;
4、镜检后,可根据具体研究需要及方法进行细胞常规培养。
注意事项
1、使用前需确保细胞冻存液完全融化,并轻轻混匀;
2、若需长期冻存细胞,请转移至液氮罐中贮存;
3、冻存干细胞或原代细胞时,建议事先使用该产品对所冻存的细胞进行为期至少1周的预实验,确认性能后再进行正式冻存;
4、为减小操作过程中交叉污染风险,建议分装使用;
5、冻存液中含有DMSO成分,为了您的安全和健康,请穿实验服并戴一次性手套操作;
6、本产品仅限科研使用。
This product is a pre-sterilized, ready-to-use cryopreservation solution designed for the low-temperature freezing of cultured cells. After harvesting the cells to be preserved, simply add an appropriate amount of this solution and mix thoroughly—no additional preparation is required. It is highly convenient and suitable for cryopreserving most types of mammalian cells.
Features
High Quality: Ensures cell resuscitation rates of over 90%.
Ease of Use: Stable storage at 2–8°C; no freezing required—ready to use directly.
Instructions for Use
Cell Freezing Procedure
Harvest adherent or suspension cells in the logarithmic growth phase and perform cell counting.
Transfer the cell suspension containing the desired number of cells into a centrifuge tube. Centrifuge to pellet the cells (recommended conditions: 1,000–2,000 rpm, 3–5 min). Carefully remove the supernatant.
Add an appropriate amount of cryopreservation solution to the tube and adjust the cell concentration to 1–5×10⁶ cells/mL. Mix gently to prepare a uniform cell suspension.
Dispense the cell suspension into clearly labeled cryovials.
Place the cryovials in a device capable of controlled cooling (e.g., a programmed freezing container) and transfer to a -80°C freezer, ensuring a cooling rate of approximately 1°C/min. The cooling rate should generally not exceed 0.5°C/min.
For long-term storage in liquid nitrogen, transfer cryovials to a liquid nitrogen tank after overnight storage at -80°C.
Cell Thawing Procedure
Remove frozen cryovials and immediately thaw in a 37°C water bath with gentle agitation.
Once completely thawed, promptly transfer the cell mixture to a centrifuge tube containing 5 mL of cell culture medium. Centrifuge to pellet cells (recommended conditions: 1,000–2,000 rpm, 3–5 min).
Carefully aspirate the supernatant. Resuspend the cell pellet in an appropriate amount of fresh culture medium with gentle mixing. Transfer the cell suspension to a pre-prepared culture vessel.
After microscopic examination, proceed with routine cell culture according to specific research requirements.
Precautions
Ensure the cryopreservation solution is completely thawed and gently mixed before use.
For long-term cell storage, transfer cryovials to a liquid nitrogen tank.
When cryopreserving stem cells or primary cells, it is recommended to perform a preliminary test using this product for at least one week to verify performance before formal cryopreservation.
To minimize the risk of cross-contamination, aliquot the product for repeated use.
This solution contains DMSO. Wear a lab coat and disposable gloves for safety.
For research use only.
通过匹配包装上的批号来查找并下载产品的 COA,每批产品都进行了严格的验证,您可放心使用!
| 批号(Lot Number) | 证书类型 | 货号 |
|---|---|---|
| 分析证书 | C1491281 | |
| 分析证书 | C1491281 |
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