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Sf9 Insect Cells - Novagen

Spodoptera frugiperda (Sf9)), epithelial

Synonym(s):

InsectDirect System- Sf9 Cells

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About This Item

UNSPSC Code:
41106200
NACRES:
NA.81

product name

Sf9 Insect Cells - Novagen, Serum-free, adapted Sf9 cells

biological source

(Spodoptera frugiperda (Sf9))

Quality Level

manufacturer/tradename

Novagen®

storage condition

OK to freeze

growth mode

adherent or suspension

morphology

epithelial

technique(s)

microbiological culture: suitable

shipped in

dry ice

storage temp.

-140 to -196°C

General description

Sf9 Insect Cells are provided as frozen stocks of Spodoptera frugiperda Sf9 cells for establishment of cultures suitable for any application. These cells plus BacVector Insect Cell Medium are recommended for cotransfection of transfer plasmids with BacVector Triple Cut Virus DNA or BacMagicDNA for the construction of baculovirus recombinants and for transfection of pIEx and pBiEx vector constructs of the InsectDirect System. After recovery, they can be grown as semi-adherent cultures in tissue culture flasks or in suspension as shaker cultures. Cells are shipped on dry ice. Upon receipt, the vials should be removed from their container and either recovered immediately, or placed at -70°C and used within two weeks. For longer-term storage, place in liquid nitrogen.



Components

•: 3 vials: Sf9 Insect Cells (frozen at 1 x 10⁷ cells/ml)

Warning

Toxicity: Irritant (B)

Legal Information

INSECTDIRECT is a trademark of Merck KGaA, Darmstadt, Germany
NOVAGEN is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class

10 - Combustible liquids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificates of Analysis (COA)

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Robert Fagiewicz et al.
Structure (London, England : 1993), 30(11), 1470-1478 (2022-09-24)
Cargo adaptors are crucial in coupling motor proteins with their respective cargos and regulatory proteins. BicD2 is a prominent example within the cargo adaptor family. BicD2 is able to recruit the microtubule motor dynein to RNA, viral particles, and nuclei.
Robert L Summers et al.
Cell chemical biology, 29(2), 191-201 (2021-08-05)
We identify the Plasmodium falciparum acetyl-coenzyme A synthetase (PfAcAS) as a druggable target, using genetic and chemical validation. In vitro evolution of resistance with two antiplasmodial drug-like compounds (MMV019721 and MMV084978) selects for mutations in PfAcAS. Metabolic profiling of compound-treated parasites

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