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PeloBiotech

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www.pelobiotech.com<br />

lymphangiogenesis in a lymphatic organotypic co-culture model, providing valuable insights into the mechanisms<br />

underlying lymphatic vessel formation in the context of tumor microenvironment. Endothelial cells from the lymphatic<br />

system have been extensively studied for their role in lymphangiogenesis and the development of the lymphatic<br />

vasculature.<br />

Studies have demonstrated that Prox1 is a master control gene in the program specifying lymphatic endothelial cell fate,<br />

highlighting its essential role in the induction of the lymphatic endothelial cell phenotype. The expression of podoplanin<br />

in stromal fibroblasts has been associated with high lymphatic vessel density in triple-negative, basal marker-expressing,<br />

and high-grade breast carcinomas, indicating its potential as a marker for lymphatic endothelial cells and<br />

lymphangiogenesis. The differential response of lymphatic endothelial cells to angiopoietin-1 and angiopoietin-2 has<br />

been investigated, providing insights into the molecular regulation of lymphangiogenesis and the distinct functions of<br />

angiopoietins in lymphatic vessel development.<br />

Skeletal system<br />

We offer a variety of synovial cells, chondrocytes, osteoblasts, endothelial cells from various vessels, and tenocytes<br />

sourced from different animal species, with cell RNA from adults and fetuses all of which are extracted from various<br />

bones. Synovial cells have been studied for their modulatory effect on cell phenotype and metabolic behavior in<br />

osteoarthritic patients, providing insights into the inflammatory and metabolomic profile of synovial fluid and its impact<br />

on synovial cell behavior. Additionally, the inflammatory response of synovial fibroblasts has been investigated, shedding<br />

light on the regulation of synovial cell growth by polypeptide growth factors. Chondrocytes have been extensively utilized<br />

in the study of cartilage regeneration and the development of high-quality cartilage. Studies have focused on the potential<br />

of aged human articular chondrocytes for cartilage regeneration, aiming to reverse chondrocyte aging and enhance<br />

cartilage regeneration. Furthermore, the role of microRNA-224 in suppressing osteoblast differentiation by inhibiting<br />

SMAD4 has been investigated, providing insights into the molecular mechanisms underlying osteoblast differentiation<br />

and function.<br />

Osteoblasts have been studied for their role in bone formation and bone-related diseases, with a focus on the regulation<br />

of osteoblast proliferation and differentiation. The knockout of the BK channel in osteoblasts has been investigated to<br />

determine its impact on osteoblast function and bone formation. The proliferative actions of parathyroid hormonerelated<br />

protein (PTHrP) in chondrocytes have been studied, highlighting the role of the cyclin-dependent kinase inhibitor<br />

p57Kip2 in mediating PTHrP-induced proliferation in chondrocytes.<br />

Circulatory system<br />

We provide a diverse array of cells from different animal species, isolated from various arteries and veins. Our offerings<br />

include endothelial cells, MSCs, fibroblasts, peripheral blood cells with a variety of markers, NK cells, monocytes, and<br />

blood cells. Additionally, we offer MSCs with GFP and RFP tags, as well as smooth muscle cells, with available cell RNA.<br />

Mesenchymal stem cells (MSCs) have been extensively studied and utilized in various research and clinical applications<br />

due to their regenerative and immunomodulatory properties. MSCs have been identified and isolated from different<br />

sources, including the umbilical cord, bone marrow, adipose tissue, and other tissues. These cells have shown potential<br />

for use in tissue engineering, regenerative medicine, and immunotherapy. The expression of specific surface markers and<br />

the characterization of MSCs from various sources have been the focus of numerous studies, aiming to understand their<br />

properties and potential applications.<br />

Peripheral blood cells with a variety of markers have been extensively studied for their role in the immune response and<br />

as a source of hematopoietic stem cells. These cells have been used in the study of immune cell populations, including T<br />

cells, B cells, and natural killer (NK) cells. The expression of specific markers on peripheral blood cells has been investigated<br />

to understand their functions and to develop targeted therapies for various diseases. NK cells, a type of cytotoxic<br />

lymphocyte, have been studied for their role in the immune response against infected or malignant cells. These cells have<br />

been investigated for their potential use in cancer immunotherapy and as a treatment for viral infections. The expression<br />

of specific markers on NK cells has been studied to understand their activation and cytotoxic functions.<br />

Monocytes, which are a type of white blood cell, have been extensively studied for their role in the immune response<br />

and as precursors to macrophages and dendritic cells. These cells have been investigated for their potential use in<br />

immunotherapy and as a source of antigen-presenting cells. The expression of specific markers on monocytes has been<br />

studied to understand their differentiation and immune functions.<br />

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