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PC-12 Transfection Reagent |
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Catalog # 3229 - 0.5 mL $ 111.00
Catalog # 3230 - 1.5 mL $ 220.00
Transfection reagent for PC-12 cells
- Protocols provided for transfection of siRNA and microRNA
- High transfection efficiency
- Optimized for PC-12 (Rat Pheochromocytoma Cells)
- Kit includes Transfection Enhancer reagent and recommended transfection protocols
- Compatible with transfection in any plate format
- Reproducible transfection
- Optimized transfection protocols are adapted for use with both standard & reverse transfection methods
- Developed and manufactured by Altogen Biosystems
Transfection Efficiency:
Reagent exhibits at least 80% transfection
efficiency of siRNA delivery. Transfection efficiency
was determined by real-time RT-PCR.
Transfection Protocol:
Transfection protocols are provided with
the purchase of the reagent.
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DATA |
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Figure 1. SiRNAs targeting Lamin A/C mRNA or non-silencing control siRNA were transfected following the recommended protocol. At 48 hours post-transfection the cells were analyzed by qRT-PCR for gene expression levels. 18S rRNA levels were used to normalize the Lamin A/C data. Values are normalized to untreated sample. Data are means ± SD (n=3).
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Transfection Resource |
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siRNA Transfection || Transfection Methods || Stable Transfection || RNAi || siRNA Library Screening || RNAi Therapeutics || Cell Transfection || In Vivo Transfection Reagents || Cell Line Specific Transfection Reagents
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In Vivo Transfection Reagents || Fibroblast Cells Transfection Reagent || Astrocyte Cells Transfection Reagent || HEK-293 Transfection Reagent || MEF Transfection Reagent || HepG2 Transfection Reagent || CHO Reagent || MDA-MB Transfection Reagent || MCF-7 Reagent || PC-12 Reagent
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PC-12 (Rat Pheochromocytoma Cells) |
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PC-12 was originally derived in 1976 from a transplantable rat adrenal pheochromocytoma in 1976. PC-12 are small, have a limited amount of cytoplasm, are difficult to transfect, and have a doubling time of more than two days. These cells stop dividing and terminally differentiate when treated with nerve growth factor, which makes PC-12 cells useful as a model system for neuronal differentiation. PC-12 treated with nerve growth factor stop proliferation, grow long neuritis, and exhibit cellular composition changes that are associated with neuronal differentiation. When PC-12 differentiate, they are even more difficult to transfect. Both neuronal NO synthase and nitric oxide are required for PC12 cell differentiation. Research suggests PC-12 cells may represent a stage specific vulnerability to a known neurotoxic agent. PC-12 have a rounded morphology, tend to form clusters in culture and attach poorly to non-coated plastic surfaces, making them difficult to culture.
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