Human Peripheral Blood CD4+ T Cells

$599.00

CD4+ T cells, also known as helper T cells, are effector cells for cell-mediated immunity. Following selection and maturation in the thymus, naïve CD4+ T cells migrate to the periphery where they survey for antigens displayed by human leukocyte antigen class II (HLA-II) molecules present on the surface of professional antigen presenting cells (APCs), such as Dendritic cells (DCs), B cells, and macrophages. If the antigen presented by the HLA-II molecules is recognized as foreign, then CD4+ T cells become activated leading to the production of cytokines to initiate immune responses from other white blood cells/other immune cells of cell-mediated immunity. Furthermore, they activate the T cell-dependent branch of humoral immunity, causing the activation of B cells to produce immunoglobulin in response to the antigen. As CD4+ T cells mediate anti-tumor immunity, they are critical to cancer immunotherapy research. 

CD4+ T cells were isolated using negative immunomagnetic separation techniques and Institutional Review Board (IRB)-approved protocols and consent forms were used to acquire cells.

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CD4+ T cells, also known as helper T cells, are effector cells for cell-mediated immunity. Following selection and maturation in the thymus, naïve CD4+ T cells migrate to the periphery where they survey for antigens displayed by human leukocyte antigen class II (HLA-II) molecules present on the surface of professional antigen presenting cells (APCs), such as Dendritic cells (DCs), B cells, and macrophages. If the antigen presented by the HLA-II molecules is recognized as foreign, then CD4+ T cells become activated leading to the production of cytokines to initiate immune responses from other white blood cells/other immune cells of cell-mediated immunity. Furthermore, they activate the T cell-dependent branch of humoral immunity, causing the activation of B cells to produce immunoglobulin in response to the antigen. As CD4+ T cells mediate anti-tumor immunity, they are critical to cancer immunotherapy research. 

CD4+ T cells were isolated using negative immunomagnetic separation techniques and Institutional Review Board (IRB)-approved protocols and consent forms were used to acquire cells.

CD4+ T cells, also known as helper T cells, are effector cells for cell-mediated immunity. Following selection and maturation in the thymus, naïve CD4+ T cells migrate to the periphery where they survey for antigens displayed by human leukocyte antigen class II (HLA-II) molecules present on the surface of professional antigen presenting cells (APCs), such as Dendritic cells (DCs), B cells, and macrophages. If the antigen presented by the HLA-II molecules is recognized as foreign, then CD4+ T cells become activated leading to the production of cytokines to initiate immune responses from other white blood cells/other immune cells of cell-mediated immunity. Furthermore, they activate the T cell-dependent branch of humoral immunity, causing the activation of B cells to produce immunoglobulin in response to the antigen. As CD4+ T cells mediate anti-tumor immunity, they are critical to cancer immunotherapy research. 

CD4+ T cells were isolated using negative immunomagnetic separation techniques and Institutional Review Board (IRB)-approved protocols and consent forms were used to acquire cells.

Description

CD4+ T cells, also known as helper T cells, are effector cells for cell-mediated immunity. Following selection and maturation in the thymus, naïve CD4+ T cells migrate to the periphery where they survey for antigens displayed by human leukocyte antigen class II (HLA-II) molecules present on the surface of professional antigen presenting cells (APCs), such as Dendritic cells (DCs), B cells, and macrophages. If the antigen presented by the HLA-II molecules is recognized as foreign, then CD4+ T cells become activated leading to the production of cytokines to initiate immune responses from other white blood cells/other immune cells of cell-mediated immunity. Furthermore, they activate the T cell-dependent branch of humoral immunity, causing the activation of B cells to produce immunoglobulin in response to the antigen. As CD4+ T cells mediate anti-tumor immunity, they are critical to cancer immunotherapy research.

As a one-stop biomodeling service provider, TME offers CD4+ T-cell-based in vitro model systems:

  1. To analyze the effect of food additives on T cell activation
  2. To model CD4+ T cell polarization to assess a therapeutic’s ability to modulate T cell polarization away from pro-inflammatory phenotype and toward regulatory phenotype
  3. To assess the impact of a xenobiotic on CD4 effector differentiation and activation state
  4. To analyze CD4+ T cell exhaustion
  5. To assess Treg expansion
  6. To address the adjuvant effects of nanoparticles on the immune system based on an allogeneic co-culture model with human monocyte-derived DCs (MoDCs)
  7. To analyze T-cell activation and proliferation (MLR assay)
  8. For evaluating antigen specific responses
  9. To evaluate CD4+T cell differentiation
  10. To test the effect of immunomodulatory agents on T cell function and activation.
  11. To measure vaccine immunogenicity using the co-culture of purified DC and naïve CD4+ T cells

CD4+ T cells were isolated using negative immunomagnetic separation techniques and Institutional Review Board (IRB)-approved protocols and consent forms were used to acquire cells.

Specifications
Cat. No. CPB0011
Category Primary Cells
Organism Human (H. sapiens)
Tissue Peripheral Blood
Donor History Healthy Donor
Growth Properties Suspension, Round
Applications/Intended Use Research Use Only: This product is intended for laboratory research use only. It is not intended for any animal or human therapeutic use, any human or animal consumption, or any diagnostic use.
Volume/Unit 1 mL
Product Format Frozen
BioSafety II
Shipping or Handling Information Shipping with dry ice or liquid nitrogen
CoA Batch-specific test results will be provided with the product
Growth Conditions
  • IMDM + 10% FBS, or
  • DMEM w/ 4500mg/L D-Glucose + 10% FBS, or
  • RPMI 1640 Medium + 10% FBS
  • Cryopreservation Cryopreservation Medium (Cat. No. CT002)
    Disclaimer All of TME Scientific cell biology products are for research use ONLY and NOT for therapeutic/diagnostic applications. TME Scientific is not liable for any repercussions arising from the use of its cell biology product(s) in therapeutic/diagnostic or any other non-RUO application(s).