Express Five™ SFM
Gibco™

Express Five™ SFM

Express Five™ SFM ist ein Protein- und Serum-freies Medium, das speziell für die Langzeitkultivierung von High Five™ (BTI-TN-5B1-4) Zellen inWeitere Informationen
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KatalognummerMenge
104860251000 mL
Katalognummer 10486025
Preis (EUR)
146,65
Exklusiv online
181,00
Ersparnis 34,35 (19%)
Each
Menge:
1000 mL
Customize this product
Preis (EUR)
146,65
Exklusiv online
181,00
Ersparnis 34,35 (19%)
Each
Express Five™ SFM ist ein Protein- und Serum-freies Medium, das speziell für die Langzeitkultivierung von High Five™ (BTI-TN-5B1-4) Zellen in Suspension entwickelt wurde. Diese werden in Baculovirus-Expressions-Vektor-Systemen (BEVS) verwendet. Dieses Medium erfordert vor der Verwendung die Zugabe von 18 mM L-Glutamin. Merkmale von Gibco™ Express Five™ SFM:

• Herausragendes langfristiges Suspensionswachstum von High Five™ Zellen
• proteinfreie, serumfreie Rezeptur
• Optimiert für rekombinante Proteinproduktion
• Skalierbar im CelliGen™-Bioreaktor und WAVE Bioreaktor™-System

Überlegenes Wachstum von High Five™ Zellen
Gibco™ Express Five™ SFM liefert Spitzenzelldichten von bis zu 6 × 106 lebensfähigen Zellen pro ml in Schüttlerkulturen. Zellen, die an andere handelsübliche Serum-freie Medien angepasst sind, können in der Regel ohne weitere Anpassung direkt in Gibco™ Express Five™ SFM subkultiviert werden (siehe Abbildung). Zellen erfordern in der Regel eine Anpassung von serumhaltigen Rezepturen.

Die proteinfreie, serumfreie Rezeptur
Gibco™ Express Five™ SFM ist eine proteinfreie und serumfreie Rezeptur, die eine einfachere Reinigung Ihres Proteins von Interesse ermöglicht.

Optimiert für rekombinante Proteinexpression
Gibco™ Express Five™ SFM ist optimiert für die Produktion von Proteinen mit dem Baculovirus-Expressionsvektorsystem (BEVs). Mit BEVs erreichen wir routinemäßig eine rβ-Galactosidase-Proteinexpression von bis zu 1,7 U/Zelle, eine signifikante Verbesserung gegenüber anderen Medien (siehe Abbildung)

Skalierbar im CelliGen™ Bioreaktor und WAVE Bioreactor™ System
Proteinproduktion mit Gibco™ Express Five™ SFM kann in Bioreaktoren wie dem 5 l CelliGen™ Bioreaktor und dem WAVE Bioreactor™ System skaliert werden. Die entsprechende Rotor- oder Schüttlerdrehzahl und die Impfdichte sollten für jedes System optimiert werden. Je nach Bioreaktordesign kann es erforderlich sein, Gibco™ Express Five™ SFM mit zusätzlichem Pluronic™ F-68 zu ergänzen, um pure Belastungen in der Kultur zu vermeiden.

Das cGMP-Herstellungs- und Qualitätssystem
Gibco™ Express Five™ SFM wird in einem cGMP-konformen Werk in Grand Island, New York, hergestellt. Die Einrichtung ist von der US-Arzneimittelbehörde FDA als Hersteller von Medizinprodukten zugelassen und nach ISO 13485-zertifiziert.
Nur für Forschungszwecke. Nicht zur Verwendung bei diagnostischen Verfahren.
Specifications
ZelllinieHigh Five™
ZelltypInsektenzelle, Insektenzelle
ProduktlinieExpress Five, Gibco, Express Five, Gibco
ProdukttypSerumfreies Medium (SFM) für Insektenzellen
Menge1000 mL
VersandbedingungRaumtemperatur
KlassifikationProtein-frei, Serum-frei, Serum-frei
FormFlüssig
Serum LevelSerumfrei
Ohne AdditiveKein Glutamin
Unit SizeEach
Inhalt und Lagerung
Lagerbedingungen: 2 – 8 °C. Vor Licht schützen
Versandbedingungen: Raumtemperatur
Haltbarkeit: 18 Monate ab Herstellungsdatum

Häufig gestellte Fragen (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 the glutamine requirement so high for Express Five media?

The glutamine concentration is correct. Insect media have historically been 2 to 10 fold higher in glutamine concentration vs. classical mammalian media. Express Five SFM was optimized for High Five cells which have especially high requirements for glutamine and asparagine. The liquid basal media is actually 1.09x in concentration and was designed to be diluted to the correct 1x composition with 90 ml/L of the 200 ml L-glutamine. Because the L-glutamine concentration is so high, we left it out of the basal formulation to avoid problems associated with glutamine degradation and the resulting ammonia build-up which can be toxic.

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

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 I use antibiotics such as Pen-Strep in Express Five SFM?

Many antibiotics are suitable for use with insect cells. The table on page 11 of the manual (https://assets.thermofisher.com/TFS-Assets/LSG/manuals/Insect_Cell_Lines_UG.pdf) summarizes some of the most commonly used antibiotics, their working concentrations, and their methods of action. Please see page 38 for ordering information.

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

Can I add GlutaMAX to Express Five SFM instead of L-Glutamine?

We recommend that you use L-Glutamine instead of GlutaMAX, as insect cells lack the ability to sufficiently cleave the dipeptide bond in the GlutaMax, making it a poor source of glutamine for these cells.

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

Zitierungen und Referenzen (2)

Zitierungen und Referenzen
Abstract
Asp-225 and glu-375 in autocatalytic attachment of the prosthetic heme group of lactoperoxidase.
Authors: Colas Christophe; Kuo Jane M; Ortiz de Montellano Paul R;
Journal:J Biol Chem
PubMed ID:11756449
The heme in lactoperoxidase is attached to the protein by ester bonds between the heme 1- and 5-methyl groups and Glu-375 and Asp-275, respectively. To investigate the cross-linking process, we have examined the D225E, E375D, and D225E/E375D mutants of bovine lactoperoxidase. The heme in the E375D mutant is only partially ... More
The type XIII collagen ectodomain is a 150-nm rod and capable of binding to fibronectin, nidogen-2, perlecan, and heparin.
Authors: Tu Hongmin; Sasaki Takako; Snellman Anne; Göhring Walter; Pirilä Paivi; Timpl Rupert; Pihlajaniemi Taina;
Journal:J Biol Chem
PubMed ID:11956183
Type XIII collagen consists of a short N-terminal intracellular domain, a transmembrane domain, and a collagenous ectodomain, and it is found at many sites of cell adhesion. We report on the characterization of recombinant type XIII collagen. The shed ectodomain was purified from insect cell culture medium and shown to ... More