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ClonaCell™-CHO ACF培养基

无动物成分，无血清，无谷氨酰胺半固体甲基纤维素为基础的培养基，用于选择和克隆CHO细胞
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产品号 #03816_C

无动物成分，无血清，无谷氨酰胺半固体甲基纤维素为基础的培养基，用于选择和克隆CHO细胞

产品优势

  • 动物部分流;只含有重组蛋白和合成成分
  • 与化学定义的无蛋白培养基相比，CHO细胞的单细胞克隆效率更高，特别是在低镀密度下
总览
产品说明书及文档
应用领域
相关材料与文献
相关产品

总览

ClonaCell™-CHO ACF是一种基于甲基纤维素的半固体培养基，用于在无血清条件下选择和克隆适应悬液的CHO细胞。该培养基不含动物成分，只含有重组蛋白和合成成分。与无蛋白培养基相比，这种培养基在低密度下具有更高的CHO细胞单细胞克隆效率。它不含L -谷氨酰胺、选择剂或酚红，与二氢叶酸还原酶（DHFR）和谷氨酰胺合成酶（GS）选择系统兼容。

半固体克隆的优势：

•单个细胞悬浮在粘性培养基中，形成物理上分离的离散克隆，易于分离。

•使用半固体培养基进行筛选和克隆时，相较于限制稀释法，可以在更短时间内以更少的资源分离单克隆细胞系。

•在粘性培养基中，具有不同生长速率和生产能力的克隆形成离散的克隆。因此，通过同时选择和克隆在半固体培养基中，相较于在大规模液体培养中选择，可以更容易地分离稀有且高产的克隆。

包含
• 甲基纤维素 • 重组蛋白（不含动物成分） • 其他成分
 
分类
半固体培养基，专用培养基
 
细胞类型
CHO细胞
 
种属
其它细胞系
 
应用
细胞培养，半固体克隆
 
品牌
ClonaCell
 
研究领域
抗体​制备，细胞系制备，药物发现和毒理检测
 
制剂类别
不含动物成分，无血清
 

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产品说明书及文档

请在《产品说明书》中查找相关支持信息和使用说明，或浏览下方更多实验方案。

Document Type
Product Name
Catalog #
Lot #
Language
Document Type
Product Information Sheet
Product Name
ClonaCell™-CHO ACF Medium
Catalog #
03816
Lot #
All
Language
English
Document Type
Safety Data Sheet
Product Name
ClonaCell™-CHO ACF Medium
Catalog #
03816
Lot #
All
Language
English

应用领域

本产品专为以下研究领域设计，适用于工作流程中的高亮阶段。探索这些工作流程，了解更多我们为各研究领域提供的其他配套产品。

Research Area
Workflow Stages

相关材料与文献

技术资料 (8)

ClonaCell-CHO Semi-Solid Cloning Testing Guidelines
Brochure
ClonaCell-CHO Semi-Solid Cloning Testing Guidelines
Increase the Efficiency of Your Hybridoma Workflow with EasySep™ and ClonaCell™
Brochure
Increase the Efficiency of Your Hybridoma Workflow with EasySep™ and ClonaCell™
ClonaCell™ Media for Hybridoma and Cell Line Development
Brochure
ClonaCell™ Media for Hybridoma and Cell Line Development
Protocol for Cloning CHO Cell Lines Using ClonaCell™-CHO Semi-Solid Medium
Technical Bulletin
Protocol for Cloning CHO Cell Lines Using ClonaCell™-CHO Semi-Solid Medium
Why Use Semi-Solid Medium for Cloning Hybridomas and CHO Cells
3:39
Video
Why Use Semi-Solid Medium for Cloning Hybridomas and CHO Cells
How to Perform Semi-Solid Cloning of CHO Cell Lines in 96-Well Plates Using ClonaCell™-CHO Medium
12:47
Video
How to Perform Semi-Solid Cloning of CHO Cell Lines in 96-Well Plates Using ClonaCell™-CHO Medium
Semi-Solid Cloning of CHO Cells Using ClonaCell™-CHO Medium
10:50
Video
Semi-Solid Cloning of CHO Cells Using ClonaCell™-CHO Medium
A Smarter Way To Clone: What You Don't Know About Limiting Dilution Can Hurt Your Probability of Monoclonality
34:50
Webinar
A Smarter Way To Clone: What You Don't Know About Limiting Dilution Can Hurt Your Probability of Mon...

常见问题

Why do I get more cells when I select my fusion in liquid medium rather than in methylcellulose-based semi-solid medium?

Cells grown in liquid medium may appear to grow more rapidly than in methylcellulose-based medium. This is often due to the presence of a few rapidly growing clones that multiply quickly and become abundant in liquid culture, overgrowing clones that grow more slowly. In methylcellulose cultures, the rapidly growing cells remain in close proximity to each other, resulting in large colonies, each derived from a single fusion or transfection product. The large clones don't overgrow smaller, slower growing colonies, which can be separately isolated.

How do I thaw ClonaCell™ methylcellulose-based semi-solid medium?

We recommend thawing the medium overnight in a refrigerator at 4°C and mixing well.

How do I measure and dispense methylcellulose semi-solid medium?

We recommend using a 12 mL syringe with a 16 gauge needle attached (blunt end needles are recommended for safety purposes). Do not dispense the semi-solid media/cell mixture using serological pipettes as the media will stick to the pipette walls, resulting in inaccurate dispensed volumes and loss of cells.

My ClonaCell™ methylcellulose semi-solid medium appears runny. Why does this happen?

"Runny" methylcellulose could be a result of improper handling. Diluting the methylcellulose with too much liquid medium, or insufficient mixing before use, will result in methylcellulose with altered viscosity. Excessive condensation on the inside of the cell culture dish lid can result in water dripping onto the cultures, lowering viscosity. Additionally, bumping, shaking or other sudden movement of the culture may also disrupt the colonies. Note: methylcellulose is less viscous at room temperature than at 37°C.

What is the optimal number of colonies per plate?

We recommend 50-150 colonies per plate. As it is difficult to anticipate the numbers of colonies after a fusion or transfection, we recommend plating at three different densities to increase the likelihood of achieving a plating density of approximately 100 colonies per plate. This density allows sufficient space between the colonies to allow for easy colony picking.

There are still bubbles in the media after I plate my cells. Do I need to disrupt the bubbles?

We recommend that you avoid creating large bubbles during plating, but there is no need to manually pop or disperse the small bubbles after plating. They will disperse over the incubation period of 10-14 days.

Do I ever need to re-clone cultures grown with ClonaCell™ semi-solid medium?

Re-cloning is a good practice to observe and is recommended if the number of colonies in the original dishes was very high.

Once I pick the colonies and grow the cells in plates, will the residual methylcellulose interfere with characterization? For example, will I have problems doing an ELISA?

There will likely be some residual methylcellulose contamination when colonies are picked and transferred to the 96-well plate with the liquid growth medium. The concentration of methylcellulose, however, should be low enough that it should not interfere with most assays.

How important is the incubator humidity when culturing in methylcellulose-based medium?

Very important. In situations where the humidity is not high enough, we recommend that the 100 mm Petri dishes should be placed with an open dish containing sterile water inside a larger plastic container with a lid. Without very high humidity, the media will dry out over the culture period and this will impede the growth of the colonies.

Do I have to use 100 mm petri dishes or can I use other cultureware?

We recommend 100 mm Petri dishes as these have been used to develop and test ClonaCell™ semi-solid media. We have found that the surface area of these dishes allows for easy colony picking. Other sizes of dish (e.g. 6-well plates) can be used. It is important to use non-coated dishes to prevent cells from sticking to the bottom of the plate and obscuring the colonies. The volume of media plated should be adjusted to reflect the surface area of the dish being used.

Are there any selective agents in ClonaCell™-CHO ACF or ClonaCell™-CHO CD?

These media do not contain hypoxanthine, aminopterin, thymidine, glutamine, or any other selective agents or antibiotics. These media are therefore fully customizable. Both ClonaCell™-CHO ACF and ClonaCell™-CHO CD are compatible with dihydrofolate reductase (DHFR) and glutamine synthetase (GS) selection.

My cells grow fine in ClonaCell™-CHO ACF but I do not see colony growth in ClonaCell™-CHO CD. Why?

The plating density for successful colony growth in protein-free medium needs to be higher than what is recommended for medium that contains protein. The optimal plating density should be determined empirically by plating several cell densities. For example, when re-cloning established cell lines, we recommend testing 200-1000 cells per 100 mm plate for ClonaCell™-CHO ACF and testing 2000-10000 cells per 100mm dish for ClonaCell™-CHO CD.

What medium do you recommend for the expansion of clones after selection in ClonaCell™-CHO ACF or ClonaCell™-CHO CD?

CHO cells selected in either ClonaCell™-CHO ACF or ClonaCell™-CHO CD semi-solid medium can be expanded in ClonaCell™-CHO CD Liquid medium.

How many cells should I plate for cloning in ClonaCell™-CHO CD?

Cloning efficiencies vary for different clones and cell lines. For optimal cloning efficiencies, cells should be in logarithmic phase prior to plating. If you have had previous experience with cloning in a chemically defined liquid medium, plating cell concentration that would result in ~100 clones may be used to plate in semi-solid medium (e.g. If plating at 1 cell/well in a 96-well plate results in 10 wells being positive for clones, plating 1000 cells per 100mm plate in semi-solid medium would be a good starting cell concentration to test). A minimum of three plating cell concentrations is recommended. If no work has been previously done with the specific cell line, we recommend a range of 25 000 - 100,000 cells per 100 mm dish for selection and cloning after transfection, and 2000 - 10,000 cells per 100 mm dish for subcloning. Additional optimization of cell concentrations may be necessary.

Is the serum in ClonaCell™-TCS medium heat inactivated?

Yes, all serum used in ClonaCell™ is heat inactivated.

Is there any IgG in ClonaCell™ TCS?

While we don't add IgG to the ClonaCell™ media, we do add serum, which contains an undefined amount of IgG. We selectively use serum lots with low IgG levels in the production of ClonaCell™ media, however, levels vary from lot to lot. IgG levels in a specific lot of ClonaCell™ TCS medium are available in the lot-specific Certificate of Analysis.

Can ClonaCell™-TCS be used with any cell line?

A list of recommended cell lines can be found in the manual. Other cell lines may be compatible with ClonaCell™-TCS. It will be necessary, however, to determine the plating cell density and growth efficiency of the desired cells in ClonaCell™-TCS.

更多信息

更多信息
种属 Other
Contains • Methylcellulose • Recombinant proteins (animal component-free) • Other ingredients
配方类别 Animal Component-Free, Serum-Free
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