Cre-Expressing Human Lymphatic Endothelial Cells
Cre-Expressing Human Lymphatic Endothelial Cells enable vascular gene recombination studies, isolated from human lymph nodes for targeted applications.
人源与动物源原代细胞,覆盖神经、内分泌、消化、血液、免疫、呼吸、泌尿、生殖、运动 9 大系统,另含 PBMCs 与其他原代细胞。 共 905 个产品。
Cre-Expressing Human Lymphatic Endothelial Cells enable vascular gene recombination studies, isolated from human lymph nodes for targeted applications.
Cre-Expressing Human Lymphatic Fibroblasts are ideal for gene recombination studies, fibroblast lineage tracing, and Cre-lox system-based genetic modeling.
Utilize Cre-Expressing Human Mammary Epithelial Cells for lineage-specific gene recombination, epithelial tracing, and breast tissue model generation.
Apply Cre-Expressing Human Mammary Fibroblasts for fibroblast biology, gene recombination studies, and breast tissue microenvironment research.
Leverage Cre-Expressing Human Mammary Microvascular Endothelial Cells for genetic recombination models and microvascular research in breast tissue.
Leverage Cre-Expressing Human Ocular Choroid Fibroblasts for gene recombination in eye-related models and ocular disease microenvironment studies.
Employ Cre-Expressing Human Ovarian Epithelial Cells for targeted recombination, epithelial biology, and reproductive system disease modeling.
Cre-Expressing Human Ovarian Fibroblasts support Cre-loxP recombination systems, ovarian cell lineage tracing, and gene knockout validation studies.
Cre-Expressing Human Ovarian Microvascular Endothelial Cells enable targeted gene editing studies in ovarian cancer, angiogenesis, and vascular biology.
Apply Cre-Expressing Human Ovarian Smooth Muscle Cells for targeted recombination, smooth muscle biology, and reproductive system disease research.
Cre-Expressing Human Pancreatic Epithelial Cells enable gene recombination in pancreatic epithelium for disease studies in vitro and fibrosis modeling.
Cre-Expressing Human Pancreatic Fibroblasts provide gene recombination capability, supporting pancreatic disease modeling, fibrosis research, and.
Cre-Expressing Human Pancreatic Microvascular Endothelial Cells are isolated from human pancreatic tissue. Cre-Expressing Human Pancreatic Microvascular Endothelial Cells are characterized by immunofluorescent staining with antibodies of CD31, CD31/PECAM-1, or VE-Cadherin, or use of fluorescence-labeled acetylated low-density lipoprotein (DiI-Ac-LDL) uptakes. Each vial contains 5 x 105 cells in 1 ml volume. These Cells are negative for mycoplasma, bacteria, yeast, fungi, HIV-1, hepatitis B and hepatitis C.
Cre-Expressing Human Prostate Epithelial Cells enable gene editing applications in prostate epithelial biology, development, and tumorigenesis models.
Cre-Expressing Human Prostate Microvascular Endothelial Cells from ImmunoClone, supporting Cre/loxP recombination, vascular biology, and genetic studies.
Cre-Expressing Human Prostate Smooth Muscle Cells from ImmunoClone, isolated for genetic recombination, pathway analysis, and prostate disease research.
Cre-Expressing Human Proximal Tubular Epithelial Cells are engineered for efficient recombination, supporting renal biology and gene editing studies.
Employ Cre-Expressing Human Pulmonary Artery Endothelial Cells for vascular gene recombination, endothelial biology, and pulmonary disease modeling.
Leverage Cre-Expressing Human Pulmonary Artery Fibroblasts, isolated from human pulmonary artery tissue, ideal for vascular and fibroblast research.
Cre-Expressing Human Pulmonary Artery Smooth Muscle Cells allow conditional gene deletion, ideal for vascular remodeling, smooth muscle function studies.
Cre-Expressing Human Pulmonary Vein Endothelial Cells enable recombination on venous endothelium for angiogenesis and endothelial barrier research.
Cre-Expressing Human Pulmonary Vein Fibroblasts, Isolated from human pulmonary vein tissue, each vial contains >5 x 10^5 viable cells in 1 ml medium.
Cre-Expressing Human Pulmonary Vein Smooth Muscle Cells as genetic recombination tools using Cre/loxP technology for cardiovascular biology models.
Cre-expressing human retinal microvascular endothelial cells support targeted gene recombination studies in ocular biology and vascular pathology.
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