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Atopic Dermatitis Leukopak - Sanguine Biosciences

Atopic Dermatitis Leukopak

LeukoCore™ Atopic Dermatitis Leukopak products contain concentrated immune cells from donors with clinically confirmed atopic dermatitis, collected via apheresis. Ideal for high-yield studies on atopic dermatitis-related inflammation, cytokine signaling, and immune cell profiling.

Cryovial of Atopic Dermatitis PBMC - Sanguine Biosciences, Inc.

Atopic Dermatitis PBMC

Atopic Dermatitis PBMC samples are collected from clinically confirmed Atopic Dermatitis donors and cryopreserved for downstream immunology and dermatological research. Ideal for studying inflammatory pathways, immune cell responses, and therapeutic development in Atopic Dermatitis.

Cryovial of Atopic dermatitis plasma - Sanguine Biosciences

Atopic Dermatitis Plasma

Atopic Dermatitis Plasma – Cryopreserved human atopic dermatitis plasma collected from clinically confirmed donors. Atopic Dermatitis plasma is ideal for inflammation studies, cytokine profiling, and dermatology-focused biomarker research.

Cryovial of Atopic dermatitis serum - Sanguine Biosciences

Atopic Dermatitis Serum

Atopic Dermatitis Serum – Human serum samples collected from clinically confirmed atopic dermatitis donors. Ideal for dermatology, cytokine profiling, and inflammation-related research.

Atopic Dermatitis Skin Punch Biopsy - Sanguine Biosciences

Atopic Dermatitis Skin Punch Biopsy

Atopic Dermatitis Skin Punch Biopsy samples are collected from donors with atopic dermatitis and support research into skin barrier dysfunction, Th2-driven inflammation, and allergic sensitization pathways.

Atopic Dermatitis Whole Blood

Atopic Dermatitis Whole Blood

Atopic Dermatitis Whole Blood – IRB-consented fresh whole blood samples collected from donors diagnosed with atopic dermatitis. Ideal for dermatology, immunology, and inflammation-based research.

Eczema Skin Punch Biopsy - Sanguine Biosciences

Eczema Skin Punch Biopsy

Eczema Skin Punch Biopsy samples are collected from donors with clinically confirmed eczema and support studies of epidermal barrier disruption, Th2-mediated inflammation, and pruritic skin responses.