FreeStyle™ 293 Expression System
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Invitrogen™

FreeStyle™ 293 Expression System

FreeStyle™ 293 発現システムは、大量の哺乳類組み換えタンパク質を生成するための完全な懸濁細胞培養システムです。接着細胞の複数のフラスコを播種、供給、通過、および維持するための時間と労力を要するプロセスからラボを解放します(図 1詳細を見る
製品番号(カタログ番号)数量
K9000011キット
製品番号(カタログ番号) K900001
価格(JPY)
141,000
Online offer
Ends: 26-Dec-2025
235,100
割引額 94,100 (40%)
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数量:
1キット
FreeStyle™ 293 発現システムは、大量の哺乳類組み換えタンパク質を生成するための完全な懸濁細胞培養システムです。接着細胞の複数のフラスコを播種、供給、通過、および維持するための時間と労力を要するプロセスからラボを解放します(図 1)。FreeStyle™ 293発現システムは、FreeStyle™ 293-F懸濁細胞を優れた効率でトランスフェクションするように設計された陽イオン脂質製剤である293fectin™に、GIBCO™ FreeStyle™ 293発現培地を組み合わせています。FreeStyle™ 293-F 細胞 および 293fectin™は、発現システムの一部として、または個別に提供されています。

FreeStyle™ 293 発現システムは、化学的に定義されたタンパク質フリーの培地で、懸濁培養タイプの培養条件下で 293-F 細胞の増殖とトランスフェクションをサポートするために特別に開発されました(図 2)。この培地は、GlutaMAX™-I サプリメントを添加したすぐに使用可能な完全な培地で、動物由来成分を含みません。FreeStyle™ 293 発現培地は、細胞培養を無血清条件に適合させることに関連する時間とコストを大幅に削減できます。
研究用にのみ使用できます。診断用には使用いただけません。
仕様
細胞株FreeStyle™ 293-F細胞
分類血清フリー
濃度1 x 10^7細胞/mL
培養タイプ懸濁細胞培養
供給タイプTransfection
発現メカニズム細胞ベースの発現
発現システム哺乳動物
使用対象(アプリケーション)タンパク質発現
主機能タンパク質生産
製品ラインFreeStyle
製品タイプ発現システム
数量1キット
細胞タイプ293由来細胞
Unit SizeEach
組成および保存条件
FreeStyle™ 293発現システムには以下が含まれます。
  • GIBCO™ FreeStyle™ 293発現培地1 L
  • 1 x 107 FreeStyle™ 293 F 細胞(凍結)
  • 293fectin™トランスフェクション試薬1 mL
  • ™ 複合体形成用の 100 mL Opti-MEM I
  • 25 µg pCMV-Sport β-gal
保管および取り扱いに関する情報については、FreeStyle™ 293 システムマニュアルを参照してください。FreeStyle™ 293-F細胞は液体窒素中で保管してください。293fectin™トランスフェクション試薬は4 ℃で保管してください。Gibco™ FreeStyle™ 293 発現培地および Opti-MEM I を 2-8 ℃ の暗所に保管します。pCMV SPORT β-gal を -20 ℃ で保存しますすべての試薬は、適切な保管条件であれば、6カ月間安定していることが保証されています。

よくあるご質問(FAQ)

I am using your FreeStyle Max 293 Expression System and my cell viability is at most 87-90%. Is this normal? Do you have any tips to increase the cell viability? I am using 125 mL and 250 mL non-baffled, polycarbonate shaker flasks with vented caps. Will using baffled flasks help? Should I add Pluronic reagent to the medium?

Culture viability should be in the high 90% range for the seed stock that you are maintaining and growing for the transfections. After transfection, the viability will slowly decrease to the lower 90% to 80% range by about 3-6 days post-transfection and can drop more dramatically at 7 days or longer. This is when using our recommended protocol, which does not suggest any media changes or supplementation post-transfection.

A few parameters we recommend checking to assure high culture viability are: pH at ˜7.0, no visible clumping of the cells, CO2 levels at approximately 7-8% (this should be adjusted to achieve the appropriate pH), volume of culture at 40% or less of nominal flask capacity, and incubator temperature at 37 degrees C. If you have a shaker platform setup in your incubator, the platform may generate sufficient heat to increase the temperature of the incubator. We recommend using a thermometer attached to the shaker platform. Use of baffled flasks may help, if insufficient oxygenation of the cultures is suspected. We also recommend handling and storing the culture media properly, as light exposure can result in breakdown of certain media components. If you are using FreeStyle 293 Expression Medium, supplementing with Pluronic reagent is not necessary.

Find additional tips, troubleshooting help, and resources within our Protein Expression Support Center.

What is the main difference between the FreeStyle Max 293 Expression System and the FreeStyle 293 Expression System?

The two systems have the same components except for the transfection reagent and the medium supplied for formation of transfection complexes. The FreeStyle Max 293 Expression System contains FreeStyle Max Reagent and OptiPRO SFM (serum-free medium that is devoid of animal-origin components), whereas the FreeStyle 293 Expression System contains 293fectin Transfection Reagent and Opti-MEM I Reduced Serum Medium (serum-free medium but not animal-origin free).

Find additional tips, troubleshooting help, and resources within our Protein Expression Support Center.

Which vectors do you recommend for use with FreeStyle system?

Generally, any mammalian expression vector should be compatible with the FreeStyle expression system. Some of the more popular choices include pcDNA3.3-TOPO TA vector (Cat. No. K8300-01), pcDNA3.4-TOPO TA vector (Cat. no. A14697), pcDNA3.2 DEST vector (Cat. No. 12489018), pCEP vector (Cat. No. V044-50), or pcDNA4/HisMax vector (Cat. No. K864-20).

Find additional tips, troubleshooting help, and resources within our Protein Expression Support Center.

What is the difference between FreeStyle 293 Expression Medium and FreeStyle F17 Expression Medium?

FreeStyle F17 Expression Medium was designed from a different base formulation than FreeStyle 293 Expression Medium. FreeStyle F17 medium shows equal or better performance than the FreeStye 293 medium for certain cell lines and proteins. It is capable of supporting the growth of 293 and CHO cells and offers a wider variety and selection of transient cell culture media options.

Find additional tips, troubleshooting help, and resources within our Cell Culture Support Center.

引用および参考文献 (5)

引用および参考文献
Abstract
Molecular dissection of the alpha-dystroglycan- and integrin-binding sites within the globular domain of human laminin-10.
Authors:Ido H, Harada K, Futaki S, Hayashi Y, Nishiuchi R, Natsuka Y, Li S, Wada Y, Combs AC, Ervasti JM, Sekiguchi K,
Journal:J Biol Chem
PubMed ID:14701821
'The adhesive interactions of cells with laminins are mediated by integrins and non-integrin-type receptors such as alpha-dystroglycan and syndecans. Laminins bind to these receptors at the C-terminal globular domain of their alpha chains, but the regions recognized by these receptors have not been mapped precisely. In this study, we sought ... More
Biological activity of follistatin isoforms and follistatin-like-3 is dependent on differential cell surface binding and specificity for activin, myostatin, and bone morphogenetic proteins.
Authors:Sidis Y, Mukherjee A, Keutmann H, Delbaere A, Sadatsuki M, Schneyer A,
Journal:Endocrinology
PubMed ID:16627583
Follistatin (FST) and FST-like-3 (FSTL3) are activin-binding and neutralization proteins that also bind myostatin. Three FST isoforms have been described that differ in tissue distribution and cell-surface binding activity, suggesting that the FST isoforms and FSTL3 may have some nonoverlapping biological actions. We produced recombinant FST isoforms and FSTL3 and ... More
Mutation of key residues of RPE65 abolishes its enzymatic role as isomerohydrolase in the visual cycle.
Authors:Redmond TM, Poliakov E, Yu S, Tsai JY, Lu Z, Gentleman S,
Journal:Proc Natl Acad Sci U S A
PubMed ID:16150724
RPE65 is essential for isomerization of vitamin A to the visual chromophore. Mutations in RPE65 cause early-onset blindness, and Rpe65-deficient mice lack 11-cis-retinal but overaccumulate alltrans-retinyl esters in the retinal pigment epithelium (RPE). RPE65 is proposed to be a substrate chaperone but may have an enzymatic role because it is ... More
Binding of anthrax toxin to its receptor is similar to alpha integrin-ligand interactions.
Authors:Bradley KA, Mogridge J, Jonah G, Rainey A, Batty S, Young JA,
Journal:J Biol Chem
PubMed ID:14507921
The secreted protein toxin produced by Bacillus anthracis contributes to virulence of this pathogen and can cause many of the symptoms seen during an anthrax infection, including shock and sudden death. The cell-binding component of anthrax toxin, protective antigen, mediates entry of the toxin into cells by first binding directly ... More
A novel secreted endonuclease from Culex quinquefasciatus salivary glands.
Authors:Calvo E, Ribeiro JM,
Journal:J Exp Biol
PubMed ID:16809456
Previous analysis of the salivary gland transcriptome of Culex quinquefasciatus showed the potential presence of an endonuclease with sequence similarities to shrimp, crab and two tsetse salivary proteins. Indeed, not only was the cloned cDNA shown to encode an active double-stranded endonuclease, but also the same activity was demonstrated to ... More