Rat Primary Lung Microvascular Endothelial Cells

SKU:BHC16401115
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    Overview
    Click light‑blue chips for details
    Rat Primary Lung Microvascular Endothelial Cells are primary microvascular endothelial cells derived from rat lung tissue and supplied in selectable cryopreserved and flask formats. Commonly used in cell culture and flow cytometry studies.
    Species Rat
    Cell Type Endothelial Cells
    Organ System Respiratory
    Tissue Lung
    Morphology Endothelial
    Available Options

    Select the variant that best fits your experiment. Availability and lead time may vary by option.

    • Options: Format (3) - Frozen Vial (0.5 x 10^6 cells), T25 Flask, T75 Flask
    • Lead time: options listed in "Availability Content"; otherwise, there will be a column of “lead time”, other statuses may take longer.
    • Storage: Cryopreserved cells are shipped with dry ice overnight. Upon arrival, transfer frozen cells to liquid nitrogen (-180°C) immediately until ready for use. Live cell shipment is also available on request. Primary cells can never be kept at -20 °C or -80 °C freezer.
    • Shipping: Cryopreserved cells are shipped with dry ice overnight.
    • Upon receipt: store at the recommended temperature as soon as possible.
    • Sales terms and conditions: Please review prior to ordering.
    Options selector
    Catalog no. Format
    RN-6011-FV-0.5M Frozen Vial (0.5 x 10^6 cells)
    RN-6011-T25 T25 Flask
    RN-6011-T75 T75 Flask
    Field Specification
    Alternative Names RAPPUEC
    Product Type
    • Cells
    • Primary Cells
    Shipping Cryopreserved cells are shipped with dry ice overnight.
    Species Rat
    Storage Cryopreserved cells are shipped with dry ice overnight. Upon arrival, transfer frozen cells to liquid nitrogen (-180°C) immediately until ready for use. Live cell shipment is also available on request. Primary cells can never be kept at -20 °C or -80 °C freezer.

    Overview

    Rat Primary Lung Microvascular Endothelial Cells are primary microvascular endothelial cells derived from rat lung tissue. Product metadata indicate adherent growth with endothelial morphology and a reported BSL-2 handling context. Depending on the selected variant, the product may be supplied in selectable cryopreserved and flask formats (Frozen Vial (0.5 x 10^6 cells), T25 Flask, and T75 Flask) for in vitro studies that benefit from tissue-relevant cellular context.

    Key elements and design rationale

    • Source and identity reflect the stated endothelial cells model and tissue origin, supporting experiments where lung/respiratory context matters.
    • Reported classifications and phenotype descriptors include primary, microvascular, adherent growth, and endothelial morphology.
    • Selectable variants can include Frozen Vial (0.5 x 10^6 cells), T25 Flask, and T75 Flask; choose the listed format according to culture scale, handling preference, and downstream assay design.
    • Handling considerations should follow institutional practice appropriate for the reported BSL-2 classification and the datasheet associated with the selected format.

    Review the specification table and variant selector together when choosing the appropriate format for assay scale, tissue context, and downstream readouts.

    Biological background

    Endothelial cells line blood and lymphatic vessels and are central to barrier regulation, leukocyte trafficking, angiogenesis, coagulation signaling, and responses to shear or inflammatory cues. Tissue of origin can influence transport properties, junctional organization, and activation state. In this case, the stated lung tissue and respiratory context can influence morphology, baseline signaling, and assay responsiveness.

    Research relevance and current trends

    • Rat Primary Lung Microvascular Endothelial Cells can be used in assays of cell-cell adhesion remains an active area for experiments that compare tissue-specific phenotype, pathway response, or functional readouts in culture-based systems.
    • migration remains an active area for experiments that compare tissue-specific phenotype, pathway response, or functional readouts in culture-based systems.
    • Multiparametric readouts such as cell culture and flow cytometry are commonly combined to connect morphology, phenotype, and pathway-level response.

    Common research applications

    • Cell culture and condition-optimization studies to assess morphology, growth behavior, or baseline phenotype over time.
    • Flow-cytometry workflows to profile marker expression, viability, reporter-positive fractions, or phenotypic shifts.

    Changes in morphology, marker expression, proliferation, migration, barrier properties, reporter activity, or secreted factors are typically interpreted alongside matched controls and the selected culture conditions.

    Notes for experimental interpretation

    • Potential confounders include donor-to-donor variability, passage-dependent phenotypic drift, substrate effects, serum or media composition, and differences between cryopreserved and expansion-stage material.
    • Use matched controls and confirm identity with morphology- and marker-based readouts suited to the stated cell type, tissue source, and downstream assay.

    SKU:BHC16401115

    Customization & Add-ons: Can't find the cell line you need—or require a custom cell-based solution for your project? We can help you source the best match or support custom cell line services for diverse research needs, including cell line sourcing and selection (species, tissue, and disease model matching), stable cell line engineering (overexpression, knockdown, or knockout via CRISPR/Cas9, shRNA, or sgRNA), reporter gene integration (GFP, RFP, luciferase, and other fluorescent or bioluminescent constructs), genome editing and knockin (point mutations, tagged endogenous proteins, conditional alleles), inducible expression systems (Tet-On/Off and other regulatable constructs), drug resistance marker selection (puromycin, G418, hygromycin, and others), custom growth and media optimisation for specific assay requirements, scale-up production for high-throughput screening campaigns, and authentication and QC services (STR profiling, mycoplasma testing, viability assessment). Click Talk to a Scientist to submit a request, email us at support@biohippo.com, or explore our Research Services for additional support—our team will follow up with feasibility details and next steps.

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    What growth behavior or morphology should I expect?
    These cells are reported as adherent with endothelial morphology. Use that information to plan attachment conditions, imaging expectations, and routine culture workflow, while still confirming actual behavior after recovery in your own system.
    What should I confirm before ordering or starting an experiment?
    Before ordering, confirm the match between Rat, Lung Microvascular, and Primary, Microvascular and your assay design. It is also worth checking the selected format (Frozen Vial (0.5 x 10^6 cells), T25 Flask, and T75 Flask) aligns with your seeding plan, expansion needs, markers, and downstream readouts.

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