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Products > SK-N-MC Transfection Reagent (Neuroblastoma Cells)

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Presentation on theme: "Products > SK-N-MC Transfection Reagent (Neuroblastoma Cells)"— Presentation transcript:

1 Products > SK-N-MC Transfection Reagent (Neuroblastoma Cells)
Altogen labs Leading Developer and Manufacturer of In Vivo and DNA Transfection Kits, Transfection Reagents and Electroporation Delivery Products Products > SK-N-MC Transfection Reagent (Neuroblastoma Cells) Altogen Biosystems offers the SK-N-MC Transfection Reagent among a host of 100+ cell line specific In Vitro Transfection Kits. The SK-N-MC Transfection Reagent is a two-component formulation that enhances lipid-mediated transfection efficiency, and it has been developed to provide high transfection efficiency with the SK-N-MC cell line. This cell line is a good host for studying brain cancers. When cultured in vitro, SK-N-MC cells are a monolayer and adhere to the surface of the culture flask. Other applications include drug discovery, gene expression studies, molecular and cell biology research applications. Purchase SK-N-MC Transfection Kit at Altogen Biosystems  848 Rainbow Blvd #823  Las Vegas  NV   USA Telephone   Fax   

2 High Density SK-N-MC cells
Leading Developer and Manufacturer of In Vivo and DNA Transfection Kits, Transfection Reagents and Electroporation Delivery Products Products > SK-N-MC Transfection Reagent (Neuroblastoma Cells) SK-N-MC Cell Line Description and Applications The SK-N-MC cell line is of neurogenic origin and was established by J. L. Biedler in 1971 from a 14-year old female. Although it was originally thought that the cell line was derived from a supraorbital metastasis from neuroblastoma, it is now thought to be derived from an Askin’s tumor. An Askin’s tumor has a similar morphology to neuroblastoma. The SK-N-MC cell line grows as a monolayer, and the cells are adherent and fibroblast-like. The cell line has a modal number of 46 and is a pseudodiploid human cell line. This SK-N-MC cell line is a neuroblastoma cell line and is a useful tool for researching types of cancer. High Density SK-N-MC cells Altogen Biosystems  848 Rainbow Blvd #823  Las Vegas  NV   USA Telephone   Fax   

3 SK-N-MC Transfection Protocol
Leading Developer and Manufacturer of In Vivo and DNA Transfection Kits, Transfection Reagents and Electroporation Delivery Products Products > SK-N-MC Transfection Reagent (Neuroblastoma Cells) SK-N-MC Transfection Protocol 1. Plate 10, ,000 SK-N-MC cells per well in 0.5 ml of complete growth medium 12–24 hours prior to transfection 2. Wash with 1xPBS and add 0.5 ml of fresh growth medium 3. Prepare transfection complexes by mixing 40 µl of serum-free medium, 5.5 µl of transfection reagent, and • 750 ng DNA (or mRNA), or • 30 nM - 50 nM of siRNA (or microRNA) *Referred to a final volume including growth medium 4. Incubate transfection complexes at RT for minutes 5. Optional: Add 2 µl of Complex Condenser. This reagent reduces the size of transfection complex, therefore increasing transfection efficiency; however, it may increase cell toxicity 6. Add prepared transfection complexes to 0.5 ml of complete growth medium with SK-N-MC cells (from step 2) 7. Incubate cells at 37ºC in a humidified CO2 incubator 8. Assay for phenotype or target gene expression hours after transfection Optional: Transfection efficiency can be increased by addition of Transfection Enhancer reagent. Add 2 µl of Transfection Enhancer reagent hours after transfection If the viability of SK-N-MC cells being transfected is affected at hours post-transfection, the level of cytotoxicity can be decreased by changing the growth medium and eliminating redundant exposure of cells to transfectant Altogen Biosystems  848 Rainbow Blvd #823  Las Vegas  NV   USA Telephone   Fax   

4 General Lipoplex-mediated Transfection Mechanism of Action
Leading Developer and Manufacturer of In Vivo and DNA Transfection Kits, Transfection Reagents and Electroporation Delivery Products Products > SK-N-MC Transfection Reagent (Neuroblastoma Cells) General Lipoplex-mediated Transfection Mechanism of Action Altogen Biosystems  848 Rainbow Blvd #823  Las Vegas  NV   USA Telephone   Fax   

5 SK-N-MC Transfection Kit Product Details
Leading Developer and Manufacturer of In Vivo and DNA Transfection Kits, Transfection Reagents and Electroporation Delivery Products Products > SK-N-MC Transfection Reagent (Neuroblastoma Cells) SK-N-MC Transfection Kit Product Details Two-component formulation enhances lipid-mediated transfection efficiency Transfection protocols provided for transfection of proteins, DNA, mRNA, siRNA, shRNA and microRNA Transfection Enhancer reagent provided with the kit Produce higher level of recombinant protein expression with minimal disruption of normal cell function Generate physiologically relevant data you can trust Effective for plasmid DNA/siRNA co-transfection Easy-to-use transfection protocol with reproducible results Low cytotoxicity Developed and manufactured by Altogen Biosystems ( Altogen Biosystems  848 Rainbow Blvd #823  Las Vegas  NV   USA Telephone   Fax   

6 Data Products > SK-N-MC Transfection Reagent (Neuroblastoma Cells)
Leading Developer and Manufacturer of In Vivo and DNA Transfection Kits, Transfection Reagents and Electroporation Delivery Products Products > SK-N-MC Transfection Reagent (Neuroblastoma Cells) Data Figure 1. GAPD mRNA levels were quantified using real-time RT-PCR in the SK-N-MC cells transfected with siRNAs targeting GAPD or non-silencing siRNA. Forty-eight hours post-transfection, the cells were harvested and analyzed by real-time RT-PCR for GAPD mRNA expression levels. Data were normalized against the 18S rRNA signal. Control samples were either mock-transfected or untreated. Values are normalized to untreated sample. Data are means ± SD (n=5).

7 Data Products > SK-N-MC Transfection Reagent (Neuroblastoma Cells)
Leading Developer and Manufacturer of In Vivo and DNA Transfection Kits, Transfection Reagents and Electroporation Delivery Products Products > SK-N-MC Transfection Reagent (Neuroblastoma Cells) Data Figure 2. Protein expression of GAPDH in SK-N-MC cells. DNA plasmid expressing GAPDH or siRNA targeting GAPDH were transfected into SK-N-MC cells following Altogen Biosystems transfection protocol. At 72 hours post-transfection the cells were analyzed by Western Blot for protein expression levels (normalized by total protein, 10 µg of total protein loaded per each well). Untreated cells used as a negative control.

8 SK-N-MC Transfection Kit Benefits
Leading Developer and Manufacturer of In Vivo and DNA Transfection Kits, Transfection Reagents and Electroporation Delivery Products Products > SK-N-MC Transfection Reagent (Neuroblastoma Cells) SK-N-MC Transfection Kit Benefits Pre-optimized transfection protocol for SK-N-MC cell line Compatible with DNA, small RNA (siRNA, shRNA, miRNA), mRNA, and small protein complexing Free of serum and protein of animal origin Compatible with standard and reverse transfection methods (both protocols provided in the kit manual) Easy to use SK-N-MC transfection protocol ensures great performance with expedited experimental timeline Equally efficient for single or multiple transfections Can be used for transient transfection and development of stable SK-N-MC cell lines Bio-degradable after endocytosis Used for preclinical research worldwide Altogen Biosystems  848 Rainbow Blvd #823  Las Vegas  NV   USA Telephone   Fax   


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