Sf-900™ II SFM
Sf-900™ II SFM
Gibco™

Sf-900™ II SFM

Sf-900™ II SFMは、Spodoptera frugiperda(Sf9およびSf21)細胞の増殖と維持、また、バキュロウイルス発現ベクター系(BEVS詳細を見る
製品番号(カタログ番号)数量
10902096500 mL
109020881000 mL
109021046 x 1 L
製品番号(カタログ番号) 10902096
価格(JPY)
6,600
Each
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数量:
500 mL
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Sf-900™ II SFMは、Spodoptera frugiperda(Sf9およびSf21)細胞の増殖と維持、また、バキュロウイルス発現ベクター系(BEVS)を用いて発現させる組換えタンパク質の大量産生に最適化された、無血清、無タンパク質の昆虫細胞培養培地です。この培地は、浮遊培養と単層培養のどちらにも適応し、他の鱗翅目の細胞増殖にも対応します。Sf-900™ II SFMの特長:

•長期・高密度培養に優れた性能を発揮
•組換えタンパク質産生用に最適化
•無血清、無タンパク質、そのまま使用可能な培地
•バイオリアクター培養にスケールアップ可能

長期・高密度培養に優れた性能を発揮
Sf-900™ II SFMで増殖されたSpodoptera frugiperda(Sf9)細胞は、9~12 x 106細胞/mLの最大細胞密度を達成し、他社製培地やグレース培地よりも大幅に改善されています(製品マニュアルを参照)。Lymantria dispar(マイマイガ)およびTrichoplusia ni(Tn-368、イラクサギンウワバ)細胞株でも、最大細胞密度の20~100%の増加が観察されています。Sf-900™ II SFMは、20継代を超える培養に対応します。

組換えタンパク質産生用に最適化
従来の組換えタンパク質の発現には、10% FBSを添加したグレース培地が使用されてきました。Sf-900™ II SFMは、Sf9および他の鱗翅目の細胞増殖、昆虫ウイルスおよびrDNAタンパク質の産生用に改良された、無血清、無タンパク質の昆虫細胞培養培地です。

無血清、無タンパク質、そのまま使用可能な培地
SF-900™ II SFMは、無血清の無タンパク質培地であるため、目的のタンパク質を簡単に精製できます。Sf-900™ II SFMはそのまま使用可能です。血清、グルタミン、界面活性剤を添加する必要はありません。他の市販の無血清培地に順応させた細胞は、通常、それ以上の順応を行わずに、直接Sf-900™ II SFMに継代できます。通常、細胞は血清含有培地からの順応が必要です。

バイオリアクター培養にスケールアップ可能
大規模細胞培養システムにおけるSf-900™ II SFMの有用性は、5 LのCelligen™ バイオリアクターで実証されています。rAcNPVによる感染を行い、rβ-GalおよびrEPOが生成されました(製品マニュアルを参照)。

製品の使用
製造プロセスでGibco™ Sf-900 II SFMをしており、FDAに申請を提出するお客様は、当社のタイプIIドラッグマスターファイル(DMF)を参照するために、当社に閲覧許可状を請求できます。
cGMP準拠の製造および品質管理システム
サプライチェーン継続性のため、Sf-900 II SFMは、ニューヨーク州グランドアイランドと英国スコットランドにある2施設で製造されています。どちらもcGMP製造要件に準拠した施設であり、ISO 13485認証を取得済みで、FDAに医療機器製造業者として登録されています。
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Sf21, Sf9
細胞タイプInsect Cell
製品ラインGibco, Sf-900
製品タイプInsect Cell Serum Free Medium (SFM)
数量500 mL
出荷条件Room Temperature
S. frugiperda, Spodoptera frugiperda
分類Protein-free, Serum-free
形状Liquid
Serum LevelSerum-free
添加剤ありGlutamine
Unit SizeEach
組成および保存条件
Storage conditions: 2°C to 8°C. Protect from light
Shipping conditions: Ambient
Shelf life: 12 months from date of manufacture

よくあるご質問(FAQ)

How do I adapt my cells to serum-free medium?

Cells can be adapted by Sequential or Direct Adaptation. Suggested protocols for each are below, and you can also find more information by searching "Adaptation of Cell Cultures to a Serum-Free Medium" from our website home page.

SEQUENTIAL ADAPTATION
1) Subculture the cells growing in serum-supplemented medium into a 25%:75% mixture of SFM and serum supplemented medium.
2) When the cell density is 5 x 10E5 cells/ml, subculture the cells into a 50%:50% mixture of SFM and serum supplemented medium at a cell density 2.5 x 10E5 to 3 x 10E5 cells/ml.
3) Continue to subculture after the cell density 5 x 10E5 cells/ml in gradually increasing proportions of SFM until the serum is ~0.1% with about 85% cell viability.
4) Subculture the cells into SFM with an innoculum of 2.5 x 10E5 to 3 x 10E5 cells/ml.
5) When the cell density is 1 x 10E6 to 3 x 10E6 cells/ml (4 to 6 days post planting) subculture the cells again.
6) Stock cultures of SFM adapted cells should be subcultured in SFM every 3 to 5 days when the cell density is 1 x 10E6 to 3 x 10E6 cells/ml with 90% viability.

DIRECT ADAPTATION
Some cells can be directly adapted from serum-containing medium to SFM. For direct adaptation, the cell innoculum should be 1.5 x 10E5 to 3 x 10E5 cells/ml.
Cells should be subcultured when the cell density is 1 x 10E6 to 3 x 10E6 cells/ml. Cells are fully adapted to SFM when the cell density is 2 x 10E6 to 4 x 10E6 cells/ml after 4 to 7 days in culture.
Stock cultures of cells adapted to SFM should be subcultured in SFM every 3 to 5 days when the cell density is 1 x 10E6 to 3 x 10E6 cells/ml with 90% viability.

Why is it necessary to gradually adapt the cells to serum-free medium?

Some cells, such as insect cells, are sensitive to changes in their medium. By sequentially adapting cells, the medium is changed with minimal effects on cell growth.

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

Can Sf9 cells in Sf-900 III SFM (Cat. No. 12659017) be thawed and grown in Sf-900 II SFM instead?

It should be okay to thaw the cells into Sf-900 II SFM. This is a richer media compared to the Sf-900 III SFM so the cells would have an easy time adapting. We would recommend taking the cells through 3 passages in the new medium before using them for any experiments as that they have enough time to adapt.

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

What antimicrobials can be used in insect culture and at what concentration?

Many antibiotics are suitable for use with insect cells. The following antibiotics are commonly used:
- Penicillin/Streptomycine: 50-100 U/mL; 50-100 µg/mL
- Amphotericin B (Fungizone antimycotic): 0.25 µg/mL
- Gentamicin: 0.5 mL of 10 mg/mL solution in 500 mL media (final concentration: 10 µg/mL)

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

Is it necessary to heat-inactivate my serum before adding it to my medium?

Heat inactivation is not necessary. Our team has routinely used serum that has not been heat-inactivated, and we have not observed any effect on cell growth or morphology.

Many cells do not require heat-inactivated FBS. Some cells prefer heat-inactivated FBS. For instance, we use heat-inactivated FBS for our insect cell lines, i.e., Sf9 and Sf21 cells.

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

引用および参考文献 (16)

引用および参考文献
Abstract
Hydrolysis of biological peptides by human angiotensin-converting enzyme-related carboxypeptidase.
Authors: Vickers Chad; Hales Paul; Kaushik Virendar; Dick Larry; Gavin James; Tang Jin; Godbout Kevin; Parsons Thomas; Baronas Elizabeth; Hsieh Frank; Acton Susan; Patane Michael; Nichols Andrew; Tummino Peter;
Journal:J Biol Chem
PubMed ID:11815627
'Human angiotensin-converting enzyme-related carboxypeptidase (ACE2) is a zinc metalloprotease whose closest homolog is angiotensin I-converting enzyme. To begin to elucidate the physiological role of ACE2, ACE2 was purified, and its catalytic activity was characterized. ACE2 proteolytic activity has a pH optimum of 6.5 and is enhanced by monovalent anions, which ... More
hsp90 is required for heme binding and activation of apo-neuronal nitric-oxide synthase: geldanamycin-mediated oxidant generation is unrelated to any action of hsp90.
Authors: Billecke Scott S; Bender Andrew T; Kanelakis Kimon C; Murphy Patrick J M; Lowe Ezra R; Kamada Yasuhiko; Pratt William B; Osawa Yoichi;
Journal:J Biol Chem
PubMed ID:11923316
'It is established that neuronal NO synthase (nNOS) is associated with the chaperone hsp90, although the functional role for this interaction has not been defined. We have discovered that inhibition of hsp90 by radicicol or geldanamycin nearly prevents the heme-mediated activation and assembly of heme-deficient apo-nNOS in insect cells. This ... More
The major conformational IgE-binding epitopes of hevein (Hev b6.02) are identified by a novel chimera-based allergen epitope mapping strategy.
Authors: Karisola Piia; Alenius Harri; Mikkola Jari; Kalkkinen Nisse; Helin Jari; Pentikäinen Olli T; Repo Susanna; Reunala Timo; Turjanmaa Kristiina; Johnson Mark S; Palosuo Timo; Kulomaa Markku S;
Journal:J Biol Chem
PubMed ID:11909866
'A novel approach to localize and reconstruct conformational IgE-binding epitope regions of hevein (Hev b6.02), a major natural rubber latex allergen, is described. An antimicrobial protein (AMP) from the amaranth Amaranthus caudatus was used as an immunologically non-IgE-binding adaptor molecule to which terminal or central parts of hevein were fused. ... More
Enhancing yield of infectious Bursal disease virus structural proteins in baculovirus expression systems: focus on media, protease inhibitors, and dissolved oxygen.
Authors: Hu Y C; Bentley W E;
Journal:Biotechnol Prog
PubMed ID:10585191
'Structural proteins of the poultry pathogen, infectious bursal disease virus (IBDV), were expressed in the baculovirus/insect cell expression system. To date, several reports have indicated that animal virus structural proteins are expressed only at low yield in this system. In this article, several factors were examined to enhance yield. These ... More
Crystal Structure of Imaginal Disc Growth Factor-2. A MEMBER OF A NEW FAMILY OF GROWTH-PROMOTING GLYCOPROTEINS FROM DROSOPHILA MELANOGASTER.
Authors: Varela Paloma F; Llera Andrea S; Mariuzza Roy A; Tormo Jose;
Journal:J Biol Chem
PubMed ID:11821393
'Imaginal disc growth factor-2 (IDGF-2) is a member of a recently described family of Drosophila melanogaster-soluble polypeptide growth factors that promote cell proliferation in imaginal discs. Although their precise mode of action has not been established, IDGFs cooperate with insulin in stimulating the growth of imaginal disc cells. We report ... More