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    iPS cell reprogramming

    Stem Cell CoreStem Cell CoreGladstone Institutes

    The core reprograms human iPS cells from peripheral blood mononuclear cells (PBMCs) or from human fibroblasts. When you start from whole blood, it isolates the PBMCs first.

    You provide

    • Starting materialPBMCs, human fibroblasts, whole blood, or an existing iPS cell line
    • Protocol or earlier data

    Request this service

    Stem Cell Core replies with scope and price.

    Your details

    Your lab *

    Find your lab

    Join your lab to use its details for future bookings and requests.

    Nothing is booked or charged until you accept a quote.

    You receive

    • Human iPS cells from your donor's blood or fibroblasts
    • PBMCs isolated from whole blood, when you start from blood

    How it goes

    1. 1

      You ask

      Answer a few questions about your samples.

    2. 2

      They scope it

      The facility confirms it can be done and may ask for a detail or two.

    3. 3

      You accept a quote

      Price and timing, agreed before any work starts.

    4. 4

      Results come back

      Files arrive in your requests, with a note from the facility.

    Where it's been used

    1. Reprogramming of blood cells (PBMCs) from identical twins discordant for macular degeneration into a genetically matched pair of iPS cell lines.

      Generation of induced pluripotent stem cell lines (RFSCi003-A, RFSCi004-A) from monozygotic twins discordant for age-related macular degeneration

      Rajendran, Runyon, Hu, et al. · Stem Cell Research · 2025

    2. iPS cell lines from a macular degeneration patient with hyperreflective foci and from an unaffected sibling, made with core staff.

      Generation of human induced pluripotent stem cell lines from an age-related macular degeneration patient with hyperreflective foci overlying drusen (RFSCi002-A) and an unaffected sibling (RFSCi001-A)

      Ashrafi, Runyon, Hu, et al. · Stem Cell Research · 2025

    3. Patient iPS cell lines from a family with childhood-onset cardiomyopathy, turned into heart muscle cells to test how an NKX2-5 variant modifies the disease.

      Oligogenic inheritance of a human heart disease involving a genetic modifier

      Gifford, Ranade, Samarakoon, et al. · Science · 2019

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    on the shoulders of giants.

    Features

    Equipment CalendarProtocol CortexCRMImpact Reporting

    Explore

    Research IndexTechniquesCommunityPlans
    McGill UniversityConcordia UniversityUniversité de MontréalPolytechnique MontréalDobson Centre for EntrepreneurshipUniversity of Alberta
    © 2026 LabGiant
    EN|FR
    Privacy PolicyTerms of Service