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PC-12 Transfection Reagent  

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.

DATA

pc12

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).

Transfection Resource

siRNA Transfection || Transfection Methods || Stable Transfection || RNAi || siRNA Library Screening || RNAi Therapeutics || Cell Transfection || In Vivo Transfection Reagents || Cell Line Specific Transfection Reagents

Featured Products

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

PC-12 (Rat Pheochromocytoma Cells)

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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