it1208 Search Results


90
Promega phycoerythrin (pe)-conjugated anti-cd4, -cd8, or -immunoglobulin m (igm) antibodies
Oral Administration of the NOS Inhibitor NMMA Inhibited Apoptosis of Spleen Lymphocytes from MRL/ lpr but not BALB/cJ Control Mice
Phycoerythrin (Pe) Conjugated Anti Cd4, Cd8, Or Immunoglobulin M (Igm) Antibodies, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/it1208/pmc09733940-108-10-16?v=Promega
Average 90 stars, based on 1 article reviews
phycoerythrin (pe)-conjugated anti-cd4, -cd8, or -immunoglobulin m (igm) antibodies - by Bioz Stars, 2026-08
90/100 stars
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90
IDAC Theranostics depleting anti–human cd4 mab it1208
Oral Administration of the NOS Inhibitor NMMA Inhibited Apoptosis of Spleen Lymphocytes from MRL/ lpr but not BALB/cJ Control Mice
Depleting Anti–Human Cd4 Mab It1208, supplied by IDAC Theranostics, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/it1208/pmc05409099-474-21-15?v=IDAC+Theranostics
Average 90 stars, based on 1 article reviews
depleting anti–human cd4 mab it1208 - by Bioz Stars, 2026-08
90/100 stars
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Oral Administration of the NOS Inhibitor NMMA Inhibited Apoptosis of Spleen Lymphocytes from MRL/ lpr but not BALB/cJ Control Mice

Journal: Journal of investigative medicine : the official publication of the American Federation for Clinical Research

Article Title: Nitric Oxide Induces Apoptosis in Spleen Lymphocytes from MRL/ lpr Mice

doi: 10.1136/jim-52-01-29

Figure Lengend Snippet: Oral Administration of the NOS Inhibitor NMMA Inhibited Apoptosis of Spleen Lymphocytes from MRL/ lpr but not BALB/cJ Control Mice

Article Snippet: To resuspend pelleted cells, 0.2 μg of phycoerythrin (PE)-conjugated anti-CD4, -CD8, or -immunoglobulin M (IgM) antibodies (Promega, Madison, WI) in 50 μL of 1% BSA in PBS was added to wells.

Techniques: Control, Marker

Apoptosis of MRL/lpr spleen lymphocyte subsets with exogenous nitric oxide in vitro. MRL/lpr spleen lymphocytes were isolated and cultured overnight in varying concentrations of Deta NONOate. Cells were harvested and analyzed for apoptosis using flow cytometry with annexin V–fluorescein isothiocyanate and phycoerythrin cell surface marker (CD4+, CD8+, and IgM+) staining. A, The results were normalized to the percentage of apoptotic cells relative to control wells (not exposed to Deta NONOate) ± standard error and were calculated from the average of five experiments. Apoptosis of subsets was reported as follows: CD4+ cells as closed circles, CD8+ cells as open inverted triangles, IgM+ cells as closed squares, and CD4−CD8−IgM− cells as open diamonds. Deta NONOate induced significant apoptosis among CD4+, CD8+, and CD4−CD8−IgM− cells (asterisk signifies p < .05). B, The results of a representative single experiment reported as the percentage of apoptotic intact cells in each subset. Subset analysis was not performed for BALB/cJ spleen lymphocytes.

Journal: Journal of investigative medicine : the official publication of the American Federation for Clinical Research

Article Title: Nitric Oxide Induces Apoptosis in Spleen Lymphocytes from MRL/ lpr Mice

doi: 10.1136/jim-52-01-29

Figure Lengend Snippet: Apoptosis of MRL/lpr spleen lymphocyte subsets with exogenous nitric oxide in vitro. MRL/lpr spleen lymphocytes were isolated and cultured overnight in varying concentrations of Deta NONOate. Cells were harvested and analyzed for apoptosis using flow cytometry with annexin V–fluorescein isothiocyanate and phycoerythrin cell surface marker (CD4+, CD8+, and IgM+) staining. A, The results were normalized to the percentage of apoptotic cells relative to control wells (not exposed to Deta NONOate) ± standard error and were calculated from the average of five experiments. Apoptosis of subsets was reported as follows: CD4+ cells as closed circles, CD8+ cells as open inverted triangles, IgM+ cells as closed squares, and CD4−CD8−IgM− cells as open diamonds. Deta NONOate induced significant apoptosis among CD4+, CD8+, and CD4−CD8−IgM− cells (asterisk signifies p < .05). B, The results of a representative single experiment reported as the percentage of apoptotic intact cells in each subset. Subset analysis was not performed for BALB/cJ spleen lymphocytes.

Article Snippet: To resuspend pelleted cells, 0.2 μg of phycoerythrin (PE)-conjugated anti-CD4, -CD8, or -immunoglobulin M (IgM) antibodies (Promega, Madison, WI) in 50 μL of 1% BSA in PBS was added to wells.

Techniques: In Vitro, Isolation, Cell Culture, Flow Cytometry, Marker, Staining, Control