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Tumor Cell Lines

Alpha TC1-9

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Tissue: Pancreas; Alpha cell. Mouse islet cell adenoma. Alpha TC1 clone 9 is a pancreatic alpha cell line cloned from the alpha TC1 cell line which was derived from an adenoma created in transgenic mice expressing the SV40 large T antigen oncogene under the control of the rat prepro RI B promoter. This cell line […]
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Product Code

alpha TC1 clone 9; alphaTC clone 9; alpha-TC1.9; alphaTC1.9; alpha-TC1-9; aTC1 Clone 9; aTC1-9

Species

Mouse. (C57BL/6J X DBA/2)F2 (Transge

Cat.No

ABC-TC230S

Product Category Tumor Cell Lines
Size/Quantity

1 vial

Cell Type

α Cell

Shipping Info

Dry Ice

Growth Conditions

37 ℃, 5% CO2

Source Organ

Pancreas

Disease

Islet Cell Adenoma

Storage

Liquid Nitrogen

Product Type

Mouse Pancreas Cancer Cell Lines

Description

Alpha TC1-9Alpha TC1-9 is a murine pancreatic alpha-cell model derived from an islet cell adenoma in transgenic mice (C57BL/6 × DBA/2 hybrids), immortalized using the SV40 large T antigen. These cells exhibit epithelial-like morphology and adherent growth properties. Cytogenetic analysis reveals aneuploidy, yet this line retains key alpha-cell functions, including glucagon secretion regulated by extracellular glucose concentrations. Alpha TC1-9 exhibits MHC heterozygosity reflective of its mixed parental background. Unlike its progenitor, Alpha TC1, this subclone does not express insulin or preproinsulin mRNA, making it a specific model for alpha-cell function without beta-cell interference. The cell line serves as a critical tool for studying alpha-cell physiology, chemical toxicity, and transdifferentiation mechanisms.

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Citation

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Application

  • The Alpha TC1-9 cell line offers a versatile platform for exploring multiple aspects of pancreatic alpha-cell biology. It facilitates detailed investigations of glucagon biosynthesis, biosynthesis, glucose sensing and cytokine responsiveness, contributing to a comprehensive understanding of the intricate regulation of glucose sensing and glucagon secretion. Furthermore, it plays a crucial role in elucidating the impacts of metabolism-disrupting chemicals on pancreatic endocrine function. Importantly, this cell line supports research into the transdifferentiation potential of alpha-cells into beta-cells, thus offering promising avenues for beta-cell regeneration and in diabetes research and therapeutic development.

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