Immortalized Human Corneal Endothelial Cells (IM-HCEC) provided by Innoprot have been developed by immortalizing primary human corneal endothelial cells with SV40 Large T antigen.
Immortalized cells were controlled passaging side by side with the primary cells. Primary cells go into senescence after the 3rd passage while the SV40‐tranduced cells go beyond 30 passages.
Each vial of IM-HCEC contains more than 1 million viable cells. Innoprot also offers optimized medium and reagents for the growth of IM-HCEC which are quality tested together and guaranteed to give maximum performance as a global solution for in vitro IM-HCEC culture.
Immortalized Human Corneal Epithelial Cell Line (IM-HCEpiC) provided by Innoprot have been developed by immortalizing primary human corneal epithelial cells with SV40 Large T antigen.
Immortalized cells were controlled passaging side by side with the primary cells. Primary cells go into senescence after the 3th passage while the SV40‐tranduced cells go beyond 30 passages.
Each vial of IM-HCEpiC contains more than 1 million viable cells. Innoprot also offers optimized medium and reagents for the growth of IM-HCEpC which are quality tested together and guaranteed to give maximum performance as a global solution for in vitro IM-HCEpiC culture.
Immortalized Human Dermal Microvascular Endothelial Cells (IM-HDMEC) provided by Innoprot have been developed by immortalizing primary human dermal endothelial cells with SV40 Large T antigen.
Immortalized cells were controlled passaging side by side with the primary cells. Primary cells go into senescence after the 3rd passage while the SV40‐tranduced cells go beyond 30 passages.
Each vial of IM-HDMEC contains more than 1 million viable cells. Innoprot also offers optimized medium and reagents for the growth of IM-HDMEC which are quality tested together and guaranteed to give maximum performance as a global solution for in vitro IM-HDMEC culture.
Immortalized Human Hepatic Sinusoidal Endothelial Cells (IM-HHSEC) provided by Innoprot have been developed by immortalizing primary human hepatic sinusoidal endothelial cells with SV40 Large T antigen.
Immortalized cells were controlled passaging side by side with the primary cells. Primary cells go into senescence after the 3rd passage while the SV40‐tranduced cells go beyond 30 passages.
Each vial of IM-IM-HHSEC contains more than 1 million viable cells. Innoprot also offers optimized medium and reagents for the growth of IM-IM-HHSEC which are quality tested together and guaranteed to give maximum performance as a global solution for in vitro IM-HHSEC culture.
Immortalized Human Keratocytes (IM-HK) provided by Innoprot have been developed by immortalizing primary human keratocytes (a.k.a. corneal fibroblasts) with HPV16 E6/E7 gene.
Immortalized cells were controlled passaging side by side with the primary cells. Primary cells go into senescence after the 4th passage while the HPV16 E6/E7 gene‐tranduced cells go beyond 30 passages.
Each vial of Immortalized human keratocytes contains more than 1 million viable cells. Innoprot also offers optimized medium and reagents for the growth of IM-HK which are quality tested together and guaranteed to give maximum performance as a global solution for in vitro IM-HK culture.
Immortalized Human Microglia (IM-HM) provided by Innoprot have been developed by immortalizing primary human microglia with SV40 Large T antigen.
Immortalized cells were controlled passaging side by side with the primary cells. These primary cells go into senescence after the 2nd passage while the SV40‐tranduced cells go beyond 30 passages.
Each vial of Immortalized Human Microglia contains more than 1 million viable cells. Innoprot also offers optimized medium and reagents for the growth of IM-HM which are quality tested together and guaranteed to give maximum performance as a global solution for in vitro IM-HM culture.
Immortalized Human Retinal Endothelial Cells (IM-HREC) provided by Innoprot have been developed by immortalizing primary human retinal endothelial cells with SV40 Large T antigen.
Immortalized cells were controlled passaging side by side with the primary cells. Primary cells go into senescence after the 4th passage while the SV40‐tranduced cells go beyond 30 passages.
Each vial of IM-HREC contains more than 1 million viable cells. Innoprot also offers optimized medium and reagents for the growth of IM-HREC which are quality tested together and guaranteed to give maximum performance as a global solution for in vitro IM-HREC culture.
Keratinocyte Medium Kit is a complete medium designed for optimal growth of normal human dermal-derived keratinocytes in vitro. Each Keratinocyte Medium Kit consists of the next components:
Leydig Cell Medium Kit is a complete medium designed for optimal growth of normal human Leydig Cells in vitro. Each Leydig Cell Medium Kit consists of the next components:
Macaque Aortic Endothelial Cells (MoAEC) provided by Innoprot are isolated from Cynomolgus Monkey aorta. MoAEC are cryopreserved at passage one and delivered frozen. Each vial of Macaque Aortic Endotheilal Cells contains more than 500.000 viable cells. They are guaranteed to further expand for 5 population doublings following the instructions provided in the technical sheet.
Innoprot also offers optimized medium and reagents for the growth of Macaque Aortic Endothelial Cells which are quality tested together and guaranteed to give maximum performance as a global solution for in vitro MoAEC culture.
Macrophage Medium Kit is a complete medium designed for optimal growth of normal primary macrophages in vitro. Each Macrophage Medium Kit consists of the next components:
Mammary Epithelial Cell Medium Kit is a complete medium designed for optimal growth of normal human Mammary epithelial cells in vitro. Each Mammary Epithelial Cell Medium Kit consists of the next components:
Melanocyte Medium Kit is a complete medium designed for optimal growth of normal primary melanocytes in vitro. Each Melanocyte Medium Kit consists of the next components:
Meningeal Cell Medium Kit is a complete medium designed for optimal growth of normal primary Meningeal Cells in vitro. Each Meningeal Cell Medium Kit consists of the next components:
Mesangial Cell Medium Kit is a complete medium designed for optimal growth of normal primary mesangial cells in vitro. Each Mesangial Cell Medium Kit consists of the next components:
Mesenchymal stem cell Adipogenic Differentiation Medium has been specifically developed and optimized for in vitro mesenchymal stem cell adipogenesis study. Each Culture Medium Kit consists of the next components:
500 ml of basal medium,
25 ml of fetal bovine serum
5 ml of mesenchymal stem cell adipogenic differentiation supplement