Porcine Embryonic Fibroblasts

Cat.No.: CSC-C4890L

Species: Pig

Source: Embryo

Cell Type: Fibroblast

  • Specification
  • Background
  • Scientific Data
  • Q & A
  • Customer Review
Cat.No.
CSC-C4890L
Description
Porcine Embryonic Fibroblasts from Creative Bioarray are isolated from embryonic tissue of porcine. Porcine Embryonic Fibroblasts are grown in T75 tissue culture flasks pre-coated with gelatin-based coating solution and incubated in Creative Bioarray Complete Growth Medium. The cells are shipped at passage 2. Each vial contains at least 0.5x10^6 cells per ml and is delivered frozen.
Species
Pig
Source
Embryo
Cell Type
Fibroblast
Disease
Normal
Quality Control
Porcine Primary Embryonic Fibroblasts are tested for negative expression of von Willebrand Factor Expression/Factor VIII, cytokeratin 18, and alpha smooth muscle actin. Porcine Primary Embryonic Fibroblasts are negative for bacteria, yeast, fungi, and mycoplasma. Cells can be expanded for 3-5 passages at a split ratio of 1:2 under the cell culture conditions specified by Creative Bioarray. Repeated freezing and thawing of cells is not recommended.
Storage and Shipping
Creative Bioarray ships frozen cells on dry ice. On receipt, immediately transfer frozen cells to liquid nitrogen (-180 °C) until ready for experimental use.
Never can cryopreserved cells be kept at -20 °C.
Citation Guidance
If you use this products in your scientific publication, it should be cited in the publication as: Creative Bioarray cat no. If your paper has been published, please click here to submit the PubMed ID of your paper to get a coupon.

Porcine Embryonic Fibroblasts (PEFs) are a cornerstone of advanced biotechnology, serving as the premier cellular substrate for genetic engineering, nuclear transfer, and basic developmental biology. Derived from the embryonic tissue of Sus scrofa, PEFs represent a highly plastic and robust cell population that bridges the gap between fundamental research and large-scale agricultural or biomedical applications.

  • Optimal Substrate for Somatic Cell Nuclear Transfer (SCNT): PEFs are the "gold standard" donor cells for porcine cloning. Their high efficiency in genomic reprogramming makes them indispensable for producing transgenic pigs, which serve as crucial models for human disease and pioneers in xenotransplantation research.
  • Superior Genetic Maneuverability: These cells exhibit exceptional resilience to genetic interventions, including CRISPR/Cas9 mediated gene editing, viral transduction, and stable transfection. PEFs maintain high viability post-selection, ensuring the successful generation of precise genetic modifications.
  • Feeder Layer Excellence: In the field of stem cell research, PEFs are frequently utilized as highly effective feeder layers. They provide a rich secretome of essential growth factors and extracellular matrix components that support the undifferentiated growth and pluripotency of porcine induced pluripotent stem cells (piPSCs) and embryonic stem cells (ESCs).
  • High Translational Relevance: The physiological, anatomical, and genomic similarities between swine and humans make PEFs a superior model compared to rodent fibroblasts. They provide a more predictive platform for evaluating cellular responses to drugs, toxins, and metabolic stressors in a human-proximal context.

Validated for rapid doubling times and consistent morphology, our Porcine Embryonic Fibroblasts undergo rigorous quality control to ensure they are free from mycoplasma and common porcine pathogens. By providing a standardized, "reprogramming-ready" cell system, this product is an essential asset for laboratories and biotech firms focused on genome editing, regenerative medicine, and the development of next-generation animal models.

Establishment, Characterization, and Validation of Porcine Embryonic Fibroblasts as A Potential Source for Genetic Modification

Fibroblasts are the common cell type in the connective tissue-the most abundant tissue type in the body. Fibroblasts are widely used for cell culture, for the generation of induced pluripotent stem cells (iPSCs), and as nuclear donors for somatic cell nuclear transfer (SCNT). We report for the first time, the derivation of embryonic fibroblasts (EFs) from porcine embryonic outgrowths, which share similarities in morphology, culture characteristics, molecular markers, and transcriptional profile to fetal fibroblasts (FFs). We demonstrated the efficient use of EFs as nuclear donors in SCNT, for enhanced post-blastocyst development, implantation, and pregnancy outcomes. We further validated EFs as a source for CRISPR/Cas genome editing with overall editing frequencies comparable to that of FFs. Taken together, we established an alternative and efficient pipeline for genome editing and for the generation of genetically engineered animals.

In vivo developmental potential of cloned embryos generated from embryonic fibroblasts.

Fig. 1. In vivo development of 40-day fetuses with the use of EF as nuclear donor cells in SCNT (Park, Chi-Hun, et al., 2022).
Difference between cell culture dish and culture flask?

In terms of cell culture status, there is not much difference between culture flasks and Petri dishes, mainly because of the safety factor (flasks > Petri dishes) and the number of cultured cells (large flasks > Petri dishes). However, the cost of culture flasks will be relatively high, so no special requirements, generally choose the Petri dish can be.

Ask a Question

Average Rating: 5.0    |    1 Scientist has reviewed this product

Worth paying more

From the use of Creative Bioarray's cell products, we have established a good relationship.

12 Aug 2023


Ease of use

After sales services

Value for money


Write your own review

For research use only. Not for any other purpose.

Hot Products