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cd4 antibody  (NSJ Bioreagents)


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    Structured Review

    NSJ Bioreagents cd4 antibody
    Cd4 Antibody, supplied by NSJ Bioreagents, used in various techniques. Bioz Stars score: 99/100, based on 10065 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/cd4 antibody/product/NSJ Bioreagents
    Average 99 stars, based on 10065 article reviews
    cd4 antibody - by Bioz Stars, 2026-02
    99/100 stars

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    <t>CD4</t> + T cells apoptosis is increased and correlated with ER stress. A – D The rate of apoptosis of CD4 + T cells was measured by the ratio of Annexin V-positive and PI-positive/negative CD4 + T cells. E – F The expression level of bax, bcl2, and caspase 3 were examined by Western blotting. G – H The expression level of GRP78and CHOP, the marker of ER stress was measured by western blotting. I – K The microstructure images of ER of CD4 + T cells in WT, WT + CLP, and CLP + 4-PBA mice were observed with electron microscopy. Green arrows represent normal-sized ER. Yellow arrows represent dilation and vesiculation of the ER. Densitometric quantification for expression of protein was normalized to ACTIN protein level. Means ± standard deviations (SDs) of four mice per group are shown. It was deemed statistically significant when P < 0.05. * P < 0.05.* P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001
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    <t>CD4</t> + T cells apoptosis is increased and correlated with ER stress. A – D The rate of apoptosis of CD4 + T cells was measured by the ratio of Annexin V-positive and PI-positive/negative CD4 + T cells. E – F The expression level of bax, bcl2, and caspase 3 were examined by Western blotting. G – H The expression level of GRP78and CHOP, the marker of ER stress was measured by western blotting. I – K The microstructure images of ER of CD4 + T cells in WT, WT + CLP, and CLP + 4-PBA mice were observed with electron microscopy. Green arrows represent normal-sized ER. Yellow arrows represent dilation and vesiculation of the ER. Densitometric quantification for expression of protein was normalized to ACTIN protein level. Means ± standard deviations (SDs) of four mice per group are shown. It was deemed statistically significant when P < 0.05. * P < 0.05.* P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001
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    <t>CD4</t> + T cells apoptosis is increased and correlated with ER stress. A – D The rate of apoptosis of CD4 + T cells was measured by the ratio of Annexin V-positive and PI-positive/negative CD4 + T cells. E – F The expression level of bax, bcl2, and caspase 3 were examined by Western blotting. G – H The expression level of GRP78and CHOP, the marker of ER stress was measured by western blotting. I – K The microstructure images of ER of CD4 + T cells in WT, WT + CLP, and CLP + 4-PBA mice were observed with electron microscopy. Green arrows represent normal-sized ER. Yellow arrows represent dilation and vesiculation of the ER. Densitometric quantification for expression of protein was normalized to ACTIN protein level. Means ± standard deviations (SDs) of four mice per group are shown. It was deemed statistically significant when P < 0.05. * P < 0.05.* P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001
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    <t>CD4</t> + T cells apoptosis is increased and correlated with ER stress. A – D The rate of apoptosis of CD4 + T cells was measured by the ratio of Annexin V-positive and PI-positive/negative CD4 + T cells. E – F The expression level of bax, bcl2, and caspase 3 were examined by Western blotting. G – H The expression level of GRP78and CHOP, the marker of ER stress was measured by western blotting. I – K The microstructure images of ER of CD4 + T cells in WT, WT + CLP, and CLP + 4-PBA mice were observed with electron microscopy. Green arrows represent normal-sized ER. Yellow arrows represent dilation and vesiculation of the ER. Densitometric quantification for expression of protein was normalized to ACTIN protein level. Means ± standard deviations (SDs) of four mice per group are shown. It was deemed statistically significant when P < 0.05. * P < 0.05.* P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001
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    <t>CD4</t> + T cells apoptosis is increased and correlated with ER stress. A – D The rate of apoptosis of CD4 + T cells was measured by the ratio of Annexin V-positive and PI-positive/negative CD4 + T cells. E – F The expression level of bax, bcl2, and caspase 3 were examined by Western blotting. G – H The expression level of GRP78and CHOP, the marker of ER stress was measured by western blotting. I – K The microstructure images of ER of CD4 + T cells in WT, WT + CLP, and CLP + 4-PBA mice were observed with electron microscopy. Green arrows represent normal-sized ER. Yellow arrows represent dilation and vesiculation of the ER. Densitometric quantification for expression of protein was normalized to ACTIN protein level. Means ± standard deviations (SDs) of four mice per group are shown. It was deemed statistically significant when P < 0.05. * P < 0.05.* P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001
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    CD4 + T cells apoptosis is increased and correlated with ER stress. A – D The rate of apoptosis of CD4 + T cells was measured by the ratio of Annexin V-positive and PI-positive/negative CD4 + T cells. E – F The expression level of bax, bcl2, and caspase 3 were examined by Western blotting. G – H The expression level of GRP78and CHOP, the marker of ER stress was measured by western blotting. I – K The microstructure images of ER of CD4 + T cells in WT, WT + CLP, and CLP + 4-PBA mice were observed with electron microscopy. Green arrows represent normal-sized ER. Yellow arrows represent dilation and vesiculation of the ER. Densitometric quantification for expression of protein was normalized to ACTIN protein level. Means ± standard deviations (SDs) of four mice per group are shown. It was deemed statistically significant when P < 0.05. * P < 0.05.* P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001

    Journal: Inflammation Research

    Article Title: mTOR pathway mediates the endoplasmic reticulum stress -apoptosis of CD4+ T cell through inhibiting autophagy flux in sepsis

    doi: 10.1007/s00011-025-02114-4

    Figure Lengend Snippet: CD4 + T cells apoptosis is increased and correlated with ER stress. A – D The rate of apoptosis of CD4 + T cells was measured by the ratio of Annexin V-positive and PI-positive/negative CD4 + T cells. E – F The expression level of bax, bcl2, and caspase 3 were examined by Western blotting. G – H The expression level of GRP78and CHOP, the marker of ER stress was measured by western blotting. I – K The microstructure images of ER of CD4 + T cells in WT, WT + CLP, and CLP + 4-PBA mice were observed with electron microscopy. Green arrows represent normal-sized ER. Yellow arrows represent dilation and vesiculation of the ER. Densitometric quantification for expression of protein was normalized to ACTIN protein level. Means ± standard deviations (SDs) of four mice per group are shown. It was deemed statistically significant when P < 0.05. * P < 0.05.* P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001

    Article Snippet: The splenocyte suspension was incubated with CD4 + antibody (CD4 + T cells isolation Kit, mouse Miltenyi, 130–104-454), washed, and passed through a separation column for negative screening, and finally centrifuged to obtain CD4 + T cells.

    Techniques: Expressing, Western Blot, Marker, Electron Microscopy

    The role of mTOR in ER stress-induced CD4 + T cells apoptosis. A – C Proteins of mTOR pathway, including mTOR, P -mTOR, downstream effectors p70s6k, p-p70s6k were examined by Western blotting. D – E The expression level of GRP78and CHOP, the marker of ER stress was measured by western blotting. F – H The expression level of bax, bcl2, and caspase 3 were examined by Western blotting. Means ± standard deviations (SDs) of four mice per group are shown. It was deemed statistically significant when P < 0.05. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001

    Journal: Inflammation Research

    Article Title: mTOR pathway mediates the endoplasmic reticulum stress -apoptosis of CD4+ T cell through inhibiting autophagy flux in sepsis

    doi: 10.1007/s00011-025-02114-4

    Figure Lengend Snippet: The role of mTOR in ER stress-induced CD4 + T cells apoptosis. A – C Proteins of mTOR pathway, including mTOR, P -mTOR, downstream effectors p70s6k, p-p70s6k were examined by Western blotting. D – E The expression level of GRP78and CHOP, the marker of ER stress was measured by western blotting. F – H The expression level of bax, bcl2, and caspase 3 were examined by Western blotting. Means ± standard deviations (SDs) of four mice per group are shown. It was deemed statistically significant when P < 0.05. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001

    Article Snippet: The splenocyte suspension was incubated with CD4 + antibody (CD4 + T cells isolation Kit, mouse Miltenyi, 130–104-454), washed, and passed through a separation column for negative screening, and finally centrifuged to obtain CD4 + T cells.

    Techniques: Western Blot, Expressing, Marker

    Deficient autophagy is observed under ER stress in sepsis and the role of mTOR on it. (A-E) With flow cytometry, the rates apoptosis of CD4 + T cells were detected in WT + CLP, mTOR KO + CLP, TSC1 KO + CLP, TSC1 KO + CLP + 4-PBA. (F, H). The expression level of LC3I/LC3II and P62, the markers of autophagy process were measured by western blotting. G , I – K Ultrastructural features of CD4 + T cells were investigated using transmission electron microscopy (TEM). In WT group, CD4 + T cells had normal morphologies, revealing baseline autophagy status. WT + CLP mice displayed increased autophagic vacuolization but no significant increase in autolysosome frequency. Large autolysosomes containing abundant contents were seen. More autophagic vacuolization and more autolysosomes were showed in mTOR KO + CLP. Autophagosomes and autolysosomes were fewer in TSC1 KO + CLP mice. Autophagosomes were double-membrane vacuoles containing cytosol or organelles (red arrow). Autolysosomes were single-membrane structures containing digested cytoplasmic components (blue arrow). Means ± standard deviations (SDs) of four mice per group are shown. It was deemed statistically significant when P < 0.05. ** P < 0.01, *** P < 0.001, **** P < 0.0001

    Journal: Inflammation Research

    Article Title: mTOR pathway mediates the endoplasmic reticulum stress -apoptosis of CD4+ T cell through inhibiting autophagy flux in sepsis

    doi: 10.1007/s00011-025-02114-4

    Figure Lengend Snippet: Deficient autophagy is observed under ER stress in sepsis and the role of mTOR on it. (A-E) With flow cytometry, the rates apoptosis of CD4 + T cells were detected in WT + CLP, mTOR KO + CLP, TSC1 KO + CLP, TSC1 KO + CLP + 4-PBA. (F, H). The expression level of LC3I/LC3II and P62, the markers of autophagy process were measured by western blotting. G , I – K Ultrastructural features of CD4 + T cells were investigated using transmission electron microscopy (TEM). In WT group, CD4 + T cells had normal morphologies, revealing baseline autophagy status. WT + CLP mice displayed increased autophagic vacuolization but no significant increase in autolysosome frequency. Large autolysosomes containing abundant contents were seen. More autophagic vacuolization and more autolysosomes were showed in mTOR KO + CLP. Autophagosomes and autolysosomes were fewer in TSC1 KO + CLP mice. Autophagosomes were double-membrane vacuoles containing cytosol or organelles (red arrow). Autolysosomes were single-membrane structures containing digested cytoplasmic components (blue arrow). Means ± standard deviations (SDs) of four mice per group are shown. It was deemed statistically significant when P < 0.05. ** P < 0.01, *** P < 0.001, **** P < 0.0001

    Article Snippet: The splenocyte suspension was incubated with CD4 + antibody (CD4 + T cells isolation Kit, mouse Miltenyi, 130–104-454), washed, and passed through a separation column for negative screening, and finally centrifuged to obtain CD4 + T cells.

    Techniques: Flow Cytometry, Expressing, Western Blot, Transmission Assay, Electron Microscopy, Membrane

    mTOR deletion activates autophagy to alleviate ER stress-induced apoptosis. (A-F) The proportion of apoptosis of CD4 + T cells were detected in WT + CLP, mTOR KO + CLP, CLP + Rap, mTOR KO + CLP + Baf, CLP + Baf by flow cytometry analysis. Densitometric quantification for expression of protein was normalized to ACTIN protein level. G – I The expression level of GRP78, CHOP, bax, and bcl2, the marker of ER stress and apoptosis were measured by western blotting. Data was presented as means ± standard deviations (SDs) of four mice per group are shown. It was deemed statistically significant when P < 0.05. ** P < 0.01, *** P < 0.001, **** P < 0.0001

    Journal: Inflammation Research

    Article Title: mTOR pathway mediates the endoplasmic reticulum stress -apoptosis of CD4+ T cell through inhibiting autophagy flux in sepsis

    doi: 10.1007/s00011-025-02114-4

    Figure Lengend Snippet: mTOR deletion activates autophagy to alleviate ER stress-induced apoptosis. (A-F) The proportion of apoptosis of CD4 + T cells were detected in WT + CLP, mTOR KO + CLP, CLP + Rap, mTOR KO + CLP + Baf, CLP + Baf by flow cytometry analysis. Densitometric quantification for expression of protein was normalized to ACTIN protein level. G – I The expression level of GRP78, CHOP, bax, and bcl2, the marker of ER stress and apoptosis were measured by western blotting. Data was presented as means ± standard deviations (SDs) of four mice per group are shown. It was deemed statistically significant when P < 0.05. ** P < 0.01, *** P < 0.001, **** P < 0.0001

    Article Snippet: The splenocyte suspension was incubated with CD4 + antibody (CD4 + T cells isolation Kit, mouse Miltenyi, 130–104-454), washed, and passed through a separation column for negative screening, and finally centrifuged to obtain CD4 + T cells.

    Techniques: Flow Cytometry, Expressing, Marker, Western Blot