Description: Fetal liver is homogenized, and then a density separation gradient media (1.077 g/ml density) is used to isolate the mononuclear cells. Next, a direct immunomagnetic CD133 MicroBead labeling system is used to positively select FL-CD133+ cells. The majority of CD133+ cells express the CD34 cell marker.

Description: First, fetal liver is homogenized. Then, a density separation gradient media (1.077g/ml density) is used to isolate the Mononuclear Cells. Next, a direct immunomagnetic CD34 MicroBead labeling system is used to positively isolate FL-CD34+ cells.

Description: Monocytes are found in the circulating peripheral blood where they make up 10-20% of the mononuclear cells. They play an important role in host defense, both as circulating monocytes and by leaving the circulation and differentiating to tissue macrophage

Description: Monocytes are found in the circulating peripheral blood where they make up 10-20% of the mononuclear cells. They play an important role in host defense, both as circulating monocytes and by leaving the circulation and differentiating to tissue macrophage

Description: Monocytes are found in the circulating peripheral blood where they make up 10-20% of the mononuclear cells. They play an important role in host defense, both as circulating monocytes and by leaving the circulation and differentiating to tissue macrophage

Description: Purified CD3+ are isolated from PBMC, include CD4+ and CD8+ subsets.

Description: Fetal liver CD36+ Early Erythroid Progenitor cells are derived from FL-CD34+ cells in culture. Fetal liver-CD34+ cells are isolated from fetal liver Mononuclear Cells with a purity 90%. FL-CD34+ cells are cultured for seven to eight days using a serum free expansion media for hematopoietic cells, with the addition of EPO (5U/ml), SCF (50ng/ml), IL-3 (10ng/ml), and IL-6 (10ng/ml) growth factors. The cells are harvested from culture, and the CD36+ cells are positively isolated, using immunomagnetic CD36 MicroBeads.

Description: Cryopreserved vial of human CD34+ cord blood iPS cells containing ≥ 500,000 cells

Description: Human CD34+ liver cells are derived from whole liver that have been dissociated into single cells and purified using magnetic cell separation. Human CD34+ liver cells are from a single donor and 95% pure populations as confirmed by FACS analysis. These cell types enable researchers to produce various cell types using standard published protocols. In addition, CD34+ cells can be used for various studies on hematopoiesis, differentiation, angiogenesis, colony formation, and surface marker expression.

Description: <divIsolated from postnatal day 8 C57BL/6 mouse sciatic nerves. MSC are cryopreserved at passage one and delivered frozen. A seeding density of andge;10,000 cells/cm^2 is recommended.andnbsp;</div

Description: SLE CD4+ T Cells are available from Gentaur. All are listed on the certificate of analysis provided with each lot.

Description: SLE CD8+ T Cells are available from Gentaur. All are listed on the certificate of analysis provided with each lot.

Description: Meningeal cells surrounding the brain participate actively in the normal development of the central nervous system. For example, they play important roles in both stabilizing the extracellular matrix of the pial surface

Description: Bone Marrow CD133+ Progenitor cells are positively isolated using a direct immunomagnetic CD133 MicroBead labeling system. The majority of CD133+ cells express the CD34 marker as well.

Description: Bone Marrow-CD34+ stem/progenitor cells are positively isolated using a direct immunomagnetic CD34 MicroBead labeling system.

Description: Mouse spleen is dissociated into a single cell suspension. The splenocytes are enriched by density separation. CD4+ T cells, CD8+T Cells, and CD19+ B Cells are isolated using specific immunomagnetic methods.

Description: NPB-CD8+ Cytotoxic T cells are negatively isolated from Mononuclear Cells using an indirect immunomagnetic CD8+ T cell labeling system.

Description: NPB-CD34+ stem/progenitor cells (NPB-CD34+) are positively isolated from mononuclear cells using an immunomagnetic CD34 MicroBead labeling system.

Description: Human CD34+ bone marrow cells are derived from whole bone marrow and purified using magnetic cell separation. Human CD34+ bone marrow cells may be from a single or multiple donors and are 95% pure populations as confirmed by FACS analysis.

Description: Cord Blood-CD19+ B cells are positively isolated from mononuclear cells, using a direct immunomagnetic CD19 MicroBeads labeling system

Description: Cord Blood CD56+ Natural Killer (NK) Cells are positively isolated from Mononuclear Cells using a direct immunomagnetic CD56 MicroBeads labeling system.

Description: Complete Growth Medium

Description: Cell lines complete growth medium

Description: Cord Blood-CD133+ Stem/Progenitor cells are positively isolated using a direct immunomagnetic CD133 MicroBead labeling system. The majority of CD133+ stem/progenitor cells express the CD34 cell marker as well. Cord Blood-CD133+ Cells/Mixed indicates that multiple donors are used to obtain the cord blood CD133+ cells

Description: Cord Blood-CD34+ Stem/Progenitor cells are positively isolated using a direct immunomagnetic CD34 MicroBead labeling system.Cord Blood-CD34+ Cells/Mixed indicates that multiple donors are pooled to obtain the cord blood CD34+ cells.

Description: Cord Blood-CD34+ Stem/Progenitor cells are positively isolated using a direct immunomagnetic CD34 MicroBead labeling system. Cord Blood-CD34+ Cells/Single indicates that only one donor is used to obtain the cord blood CD34+ cells.

Description: First, CD4+ T Cells are isolated using an indirect immunomagnetic depletion. Next, CD25+ cells are positively isolated using CD25 bright MicroBeads, leaving a highly purified CD4+ CD25+ Regulatory T Cell population.

Description: Rat spleen is mechanically dissociated into a single cell suspension. The splenocytes are enriched by density separation. CD4+ T cells, CD8+ T Cells, and CD45R+ B Cells and then isolated using specific immunomagnetic methods.

Description: Rat spleen is mechanically dissociated into a single cell suspension. The splenocytes are enriched by density separation. CD4+ T cells, CD8+ T Cells, and CD45R+ B Cells and then isolated using specific immunomagnetic methods.

Description: The development of the cerebellum involves a set of coordinated cell movements and two separate proliferation zones: the ventricular zone and the external granule cell layer (EGL), a rhombic-lip-derived progenitor pool.

Description: Human Peripheral Blood Mononuclear Cells are available as positive and negative controls for T-cell monitoring in ELISPOT, ELISA, cytokine bead array, tetramer/pentamer, and flow cytometry assays.

Description: Human Peripheral Blood Mononuclear Cells are available as positive and negative controls for T-cell monitoring in ELISPOT, ELISA, cytokine bead array, tetramer/pentamer, and flow cytometry assays.

Description: Mouse Primary Cells from Gentaur are isolated from tissue of pathogen-free laboratory mice. Mouse Cells are grown in T25 tissue culture flasks pre-coated with gelatin-based solution for 0.5 hour and incubated in Gentaur's Cell Culture Medium generally for 3-7 days. Cultures are then expanded. Prior to shipping, cells are detached from flasks and immediately cryo-preserved in vials. Each vial contains at least 1x10^6 cells per ml and is delivered frozen.Mouse Cells are negative for bacteria, yeast, fungi, and mycoplasma. Repeated freezing and thawing of cells is not recommended.Standard biochemical procedures performed with cell cultures include RT-PCR, Western blotting, immunoprecipitation, immunofluorescent staining, flow cytometry or generating cell derivatives for desired research applications.

Description: Mouse Primary Cells from Gentaur are isolated from tissue of pathogen-free laboratory mice. Mouse Cells are grown in T25 tissue culture flasks pre-coated with gelatin-based solution for 0.5 hour and incubated in Gentaur's Cell Culture Medium generally for 3-7 days. Cultures are then expanded. Prior to shipping, cells are detached from flasks and immediately cryo-preserved in vials. Each vial contains at least 1x10^6 cells per ml and is delivered frozen.Mouse Cells are negative for bacteria, yeast, fungi, and mycoplasma. Repeated freezing and thawing of cells is not recommended.Standard biochemical procedures performed with cell cultures include RT-PCR, Western blotting, immunoprecipitation, immunofluorescent staining, flow cytometry or generating cell derivatives for desired research applications.