CUSTOM CELL ISOLATION SERVICES
Are you trying to isolate a very specific cell type? Leverage our extensive expertise in cell isolation and a variety of cell isolation methods to create tailor-made products that cater to your needs.
Primary Cell Isolation
Our scientists specialize in the custom isolation of Mouse, Rat, and Human Tissues, including normal and diseased tissue, as well as peripheral blood mononuclear cells (PBMCs).

Optimize your lab’s Workflow
High viability and high-yield products tailored to your specific protocols.

TAILORED CELL ISOLATION
We offer exceptional custom primary cell isolation services for a wide range of organs, tissues, and indications, tailored to your specific protocols. Our experienced scientific team guarantees high viability and high-yield products. We specialize in isolating various primary cell types from different tissues.
IMMUNE CELLS
Human PBMCs HUman Monocytes B Cells T-Cells Mouse PBMCs
And More
TISSUE SOURCES
Subcutaneous Fat Pad
Visceral Fat Pad
ADIPOCYTE CELLS
Preadipocytes (subcutaenous) Preadipocytes (Visceral)
TISSUE SOURCES
Neonatal skin epidermis
Adult skin epidermis
KERATINOCYTES
Epidermal Keratinocytes (neonatal)
Epidermal Keratinocytes (adult)
TISSUE SOURCES
Skin dermis
Lung
Heart ventricles
HEPATOCYTES & OTHER LIVER CELLS
Hepatocytes Hepatic Stellate Cells Kuffer Cells
TISSUE SOURCES
Liver
ENDOTHELIAL CELLS
Dermal Endothelial Cells Cardiac Endothelial Cells Pulmonary Endothelial Cells
Liver Endothelial Cells Adipose Endothelial Cells
Liver Endothelial Cells Adipose Endothelial Cells
TISSUE SOURCES
Neonatal skin dermis
Heart ventricles
Lung
Liver
CARDIOMYOCYTES
Cardiomyocytes
TISSUE SOURCES
Heart
MELANOCYTES
Epidermal
Melanocytes
TISSUE SOURCES
Skin
MUSCLE CELLS
Skeletal Muscle Cells
Smooth Muscle Cells
TISSUE SOURCES
Skeletal muscle of limbs
Large and small arteries, arteriotes and veins from various tissue
EPITHELIAL CELLS
intestinal Epithelial Cells
Bronchial Epithelial Cells
Placental Epithelial Cells
Tracheal Epithelial Cells
Mammary Epithelial Cells
TISSUE SOURCES
Intestine
Bronchi
Placental amnion
Trachea
Mammary gland
RENAL CELLS
Renal Cells
TISSUE SOURCES
Kidney
STEM CELLS
Embryonic Fibroblasts
TISSUE SOURCES
Bone
OSTEOBLASTS
Osteoblasts
TISSUE SOURCES
Mouse/Rat
Embyos
Providing Deep & Robust DATA
Our scientists specialize in the custom isolation of Mouse, Rat, and Human Tissues, including normal and diseased tissue, as well as peripheral blood mononuclear cells (PBMCs).
(Top) Freshly or cryopreserved human monocytes (positive or untouched) were induced to differentiate into dendritic cells (DCs) following iXCells protocol. (Bottom) PBMCs or purified Pan T cells isolated from the corresponding donors were gently added into the wells containing DCs. 24 hours post incubation, the supernatant was collected, and performed for IFN MSD assay. The IFN release was shown by the IFN concentration calculated using the standard curve after background subtraction.

(Top) Freshly or cryopreserved human monocytes (positive or untouched) were induced to differentiate into dendritic cells (DCs) following iXCells protocol. (Bottom) PBMCs or purified Pan T cells isolated from the corresponding donors were gently added into the wells containing DCs. 24 hours post incubation, the supernatant was collected, and performed for IFNγ MSD assay. The IFNγ release was shown by the IFNγ concentration calculated using the standard curve after background subtraction.

Freshly isolated human neutrophils (Above) were incubated with the human epidermoid carcinoma cell line A431 which was stably labeled with Nuclight Red according to the various E: T ratio. The A431-Nuclight Red cell growth was monitored using InCucyte shown as Red Objective count. (Bottom Left) Representative images taken by Essence InCucyte at 72 hours co-culture; (Bottom Right) The statistic analysis of A431-Nuclight Red cell growth with or without neutrophils co-culturing at various E:T ratio.

(Top and Middle) Fresh or cryopreserved PBMCs labeled with CFSE were incubated with CD3 and CD28 antibodies. The proliferation of PBMCs were measured by decrease of the fluorescence using flow cytometry analysis. (Bottom) Human lung carcinoma cells A549 stably labeled with Nuclight Red were incubated with PBMCs, with or without the activation. The A549-Nuclight Red cell growth was monitored using InCucyte shown as Red Objective count. iXCells has set up the platform to screen the compounds which may enhance or inhibit the PBMC killing capability.

(Top and Middle) Freshly isolated human pan T cells labeled with CFSE were activated by incubating with CD3 and CD28 antibodies. The proliferation of pan T cells were measured by decrease of the fluorescence using flow cytometry analysis. (Bottom) Human lung carcinoma cells A549 stably labeled with Nuclight Red were incubated with the Pan T cells, isolated from 2 unique donors. The A549-Nuclight Red cell growth was monitored using Incucyte shown as Red Objective count. iXCells has set up the platform to screen the compounds which may enhance or inhibit the T cell killing capability.

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Discover OUR Products & additional Services
Established differentiation and marker staining protocols for a wide range of cell types, ensuring reliable and consistent results every time.
Drug discovery, drug screening, disease modeling, personalized medicine, and preclinical cell regeneration projects. Our approach allows us to develop tailored solutions that address your unique needs and accelerate the path to success.
Gene editing services using CRISPR/Cas9 technology for SNP replacement, large reporter gene knock-in, and DNA knock-out in iPSC and other cell lines. Our experts have extensive experience and can work with in-house or provided cell lines.
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