Cre-Expressing Human Colonic Epithelial Cells
Cre-Expressing Human Colonic Epithelial Cells enable conditional gene recombination, supporting colorectal biology and epithelial function analysis.
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Cre-Expressing Human Colonic Epithelial Cells enable conditional gene recombination, supporting colorectal biology and epithelial function analysis.
Leverage Cre-Expressing Human Colonic Fibroblasts for loxP-targeted gene recombination and modeling epithelial–stromal interactions in colon tissue.
Cre-Expressing Human Colonic Microvascular Endothelial Cells enable vascular gene recombination research, isolated from human colonic tissue.
Cre-Expressing Human Colonic Smooth Muscle Cells enable site-specific recombination modeling in gastrointestinal gene expression and motility studies.
Cre-Expressing Human Esophageal Epithelial Cells enable targeted gene recombination studies, isolated from human esophageal tissue for precise research.
Cre-Expressing Human Esophageal Fibroblasts enable recombination-based studies, fibrosis modeling and gene function analysis in esophageal stromal biology.
Cre-Expressing Human Esophageal Smooth Muscle Cells enable recombination studies of motility, contractility, and fibrosis in esophageal smooth muscle.
Cre-Expressing Human Intestinal Mesenteric Vascular Endothelial Cells are provided with >5×10^5 viable cells per vial, ideal for vascular research.
Leverage Cre-Expressing Human Liver Epithelial Cells, isolated from human liver tissue, each vial contains >5 x 10^5 cells, ideal for genetic research.
Leverage Cre-Expressing Human Liver Fibroblasts to support loxP recombination-based gene editing in hepatic models and liver biology applications.
Utilize Cre-Expressing Human Liver Sinusoidal Endothelial Cells for gene deletion, recombination and endothelial function studies in liver-specific models.
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 Small Intestinal Epithelial Cells enable conditional gene modification for gastrointestinal, cancer, and stem cell research.
Cre-Expressing Human Small Intestinal Fibroblasts ,Fibroblasts with Cre recombinase for lineage tracing, conditional genetics, and intestinal biology.
Cre-Expressing Human Small Intestinal Endothelial Cells enable conditional knockout studies, advancing vascular, gut, and genetic recombination research.
Cre-Expressing Human Small Intestinal Smooth Muscle Cells enable gene recombination using Cre/loxP, supporting gastrointestinal genetic research.
The Cre-Expressing Human Stomach Epithelial Cells serve as a human epithelial model for targeted gene editing and molecular pathway research.
Cre-Expressing Human Stomach Smooth Muscle Cells, stomach smooth muscle cells with Cre expression for gene recombination and gastrointestinal research.
Human CD34+ Liver Cells support hepatic progenitor studies, liver regeneration research, and stem cell-based modeling of hepatic lineage development.
Dissociated Tumor Cells are a single-cell suspension isolated from solid tumors by enzyme and mechanical separation.
Human colonic epithelial cells are CK20+ E-cadherin+ cells from colon tissue that grow tightly, support barrier, and mediate intestinal immune defense.
Human Colonic Fibroblasts from human colon are cryopreserved at P1 and support fibrosis, ECM remodeling, and gastrointestinal disease modeling.
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