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Animal Renal Proximal Tubular Epithelial Cells

2025.11.24

Renal Proximal Tubular Epithelial Cells (RPTECs) are specialized cells lining the nephron's proximal tubule[1] , crucial for kidney function. They form a selective barrier and are primarily responsible for the reabsorption of water, ions, and vital nutrients from the glomerular filtrate. These cells also actively secrete[2] [3] organic wastes and drugs, a process driven by specialized transport proteins. Due to these core functions, RPTECs are indispensable in vitro models for studying drug-induced nephrotoxicity, renal transport mechanisms, and the pathophysiology of acute kidney injury and other renal diseases.


Product Features

ü  Guaranteed High Post-Thaw Viability (≥80%)

ü  Batch-Specific Certificate of Analysis (COA)

ü  Expandable & Culture-Ready Cells

ü  Customizable: Multiple Species & Sizes

 

Product Information

Cat. No.

Product Description

Size

BM502-05

Bama Minipig Renal Proximal Tubular Epithelial Cells

0.5 million

CY502-05

Cynomolgus Monkey Renal Proximal Tubular Epithelial Cells

0.5 million

RM502-05

Rhesus Monkey Renal Proximal Tubular Epithelial Cells

0.5 million

BD502-05

Beagle Dog Renal Proximal Tubular Epithelial Cells[1] [2] 

0.5 million

Cell Morphology

Animal Renal Proximal Tubular Epithelial Cells(图1)

P1

Animal Renal Proximal Tubular Epithelial Cells(图2)

P2

Animal Renal Proximal Tubular Epithelial Cells(图3)

P3

Animal Renal Proximal Tubular Epithelial Cells(图4)

P4

Figure 1:Cyno RPTECs maintained a stable epithelial morphology through early passages (P1-P4). The cells grew as a monolayer with a characteristic cobblestone appearance, distinct cell borders, and visible intercellular connections. Across these passages, the cells demonstrated robust morphological stability without noticeable changes.

Immunofluorescence Staining

Animal Renal Proximal Tubular Epithelial Cells(图5)

Immunolocalization of β-catenin

Animal Renal Proximal Tubular Epithelial Cells(图6)

Immunolocalization of CK18



Figure 2:Cyno RPTECs (P2) were cultured for two days and then subjected to immunofluorescence staining. The cells were labeled with specific biomarkers to visualize the expression and localization of β-catenin (green, left) at adherens junctions and cytokeratin 18 (CK18, green, right) in the cytoplasm. The Nuclei were counterstained with DAPI (blue).