Description
Cell to transfect:
Designations: PC-12
Cell Synonyms: PC12, CRL-1721, pheochromocytoma, adrenal gland, rat pheochromocytoma cell
Organism: Rattus norvegicus (rat)
Tissue: pheochromocytoma; adrenal gland
Gender: male
Morphology: small irregularly shaped cells
Tumorigenic: yes, in New England Deaconess Hospital strain rats
Karyotype: 40 chromosomes; 38 autosomes plus XY
Products: catecholamines; dopamine; norepinephrine
Receptors expressed: nerve growth factor (NGF)
Growth Properties: floating clusters; few scattered lightly attached cells.
Depositor: B. Patterson
Comments: The PC-12 cell line was derived from a transplantable rat pheochromocytoma. The cells respond reversibly to NGF by induction of the neuronal phenotype when plated on Collagen IV coated culture flasks. The cells do not synthesize epinephrine.
Features of the The Transfection Reagent:
- Broad spectrum for the transfection of large plasmid, mRNA, siRNA, and/or other type of nucleic acids, which is best for co-transfection of different type and/or size of nucleic acids.
- Specifically optimized to deliver nucleic acids into PC-12 cells
- Highest efficiency to ensure experimental success
- Extremely gentle to cells
- 0.5 ml is able to transfect about 1000 wells of 24-well plate
- Deliver single or multiple plasmids
- 100% animal-free
- Compatible with serum
- Suitable for Reverse Transfection
- Compatible with transfection in any plate formats
- Reproducible: due to highly controlled chemical synthesis of each of the ingredients, the reagent forms uniformly sized complex particles with nucleic acids. With optimized protocol, our reagent will ensure the reproducible highest transfection results.
- Economical: High efficiency means less amount of nucleic acid & reagent is needed
- Developed and manufactured by EZ Biosystems
Data
FIG. 1. High throughput test of transfection efficiency (determined as RLU/mg) on PC-12 cells after transfection of luciferase reporter gene by using our 172 proprietary transfection formulas and several most popular commercial transfection reagents. The yellow box showed the results of 4 commercial transfection reagents. The red lines marked our candidate formulas with the highest transfection efficiency for PC-12 cells. This test result was confirmed with repeat experiments. The one that showed the optimal balance of potent & low cytotoxicity among those candidate formulas after flow cytometry analysis on the percentage of 7AAD positive cells was later named as this PC-12 Cell Avalanche Transfection Reagent.
For Other Cells
PC-12 Cell Avalanche® Transfection Reagent (rat pheochromocytoma cell) can also be used on the following cells with high transfection efficiencies.
786-O Cell
Caki-1 Cell
MDCK Cell
Vero Cell
293 Cell
293T/17 Cell
Recommended protocols for these cells will be provided with the reagent. The protocols usually provide satisfactory transfection efficiency with invisible cytotoxicity. However, optimization may be needed for certain type of cells. Optimizations may include: the amount of DNA and this transfection reagent; cell density; transfection reagent/DNA ratio, or incubation time for the mixture of transfection reagent/DNA etc. For best transfection result, we recommend using the respective cell type/cell line specific Avalanche transfection reagents. Those reagents have been optimized on both recipes and protocols, and have been proved to have the best transfection results for the respective cell lines or primary cells. You can easily find the respective Avalanche transfection reagents specific for your cells by using the filters of our product list.
Additional Information
Weight | 0.5 lbs |
---|---|
Adherence Phenotype |
Mixed |
Cell Type |
Others |
Disease |
Cancer |
Names starting from |
P |
Primary/Cell Line |
Cell Line |
Product Sizes |
0.5 ml, 1.5 ml |
Species |
Rat |
Tissue Sources |
Adrenal Gland |
Subcategories |
Cell Type/Cell Line Specific |
Documents
Protocols
MSDS
Citations or Feedback
- Benicky, J., Sanda, M., Brnakova Kennedy, Z., & Goldman, R. (2019). N-Glycosylation is required for secretion of the precursor to brain- derived neurotrophic factor (proBDNF) carrying sulfated LacdiNAc structures. J Biol Chem, 294(45), 16816-16830. doi:10.1074/jbc.RA119.009989