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Primary Cells

C57BL/6 Mouse Tracheal and Bronchial Epithelial Cells

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C57BL/6 Mouse Primary Tracheal and Bronchial Epithelial Cells from AcceGen are isolated from tracheal and bronchial tissue of pathogen-free laboratory mice. C57BL/6 Mouse Primary Tracheal and Bronchial Epithelial Cells are grown in a T25 tissue culture flask pre-coated with gelatin-based coating solution for 2 min and incubated in AcceGen’ Culture Complete Growth Medium for 3-5 […]
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Home | Primary Cells | Animal Primary Cells | Mouse Primary cells | C57BL/6 Mouse Tracheal and Bronchial Epithelial Cells
Species

C57BL/6 Mouse
Cat.No

ABC-TC4285
Quality Control

All cells test negative for mycoplasma, bacteria, yeast, and fungi.
Product Category Primary Cells
Size/Quantity

1 vial
Cell Type

Epithelial
Shipping Info

Dry Ice
Growth Conditions

37 ℃, 5% CO2
Source Organ

Tracheal and Bronchial
Disease

Normal
Storage

Liquid Nitrogen
Product Type

Mouse Primary Cells

Description

C57BL/6 Mouse Tracheal and Bronchial Epithelial Cells
C57BL/6 Mouse primary tracheal and bronchial epithelial cells are derived from the tracheal and bronchial tissues of pathogen-free laboratory-grade C57BL/6 mice. Following the primary culture, these cells are cryopreserved. Mouse tracheal and bronchial epithelial cells are key components of the respiratory epithelial barrier and have the functions of mucus secretion, ciliary movement, antigen presentation, and clearance of harmful particles or pathogens. Studies have shown that these cells are associated with diseases such as asthma, chronic obstructive pulmonary disease (COPD), pulmonary fibrosis, and viral infections. In vitro, these cells should be avoided repeated freezing and thawing during culture.

AcceGen Frozen Cells & Cell Lines 1 vial
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Citation

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Application

  • C57BL/6 Mouse primary tracheal and bronchial epithelial cells enable: respiratory disease modeling (asthma, COPD, cystic fibrosis) for studying pathophysiology and testing therapeutics; airway barrier function investigation against pathogens/environmental insults; drug screening to assess pharmaceutical compound effects on epithelial function; inflammatory response analysis of cytokine release, immune interactions, and signaling pathways; toxicology assessment of pollutant impacts; mucociliary clearance mechanism studies; and regenerative medicine applications for airway repair through differentiation capacity exploration.

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