rabbit anti h2b v119  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit anti h2b v119
    Rabbit Anti H2b V119, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    rabbit anti h2b v119  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit anti h2b v119
    Rabbit Anti H2b V119, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    anti h2b  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc anti h2b
    The representative western blots of β-actin, albumin, calretinin, SYPH, SYT-1, Annexin A1, ApoA4, calnexin, GNAL, GFAP, <t>H2B,</t> HSP90AB1 and vimentin shown as the expression levels in the retinas (A) and as the densitometric quantitative results (B). Equal amounts of protein from the control retinas and the I/R-treated retinas were loaded. Each lane represents individual retina (n = 4 or 6 in each group; *p<0.05 compared with the non-injured retinas). The error bars represent the standard error of the mean. C, Retinal I/R-induced reductions of the synaptic proteins SYPH and SYT-1. The representative western blots of synaptophysin (SYPH) and synaptotagmin-1 (SYT-1) shown as the expression levels in the retinas are seen in (A). The stained retinal sections of SYPH (B) and SYT-1 (C) are shown at 2 days after the injury. Blue color: DAPI stained nuclei as control. Red color: SYPH or SYT-1 positively stained synapses. The scale bar represents 50 µm. C, non-injured eyes; I/R, I/R-injured eyes.
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    1) Product Images from "Identification of Protein Network Alterations upon Retinal Ischemia-Reperfusion Injury by Quantitative Proteomics Using a Rattus norvegicus Model"

    Article Title: Identification of Protein Network Alterations upon Retinal Ischemia-Reperfusion Injury by Quantitative Proteomics Using a Rattus norvegicus Model

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0116453

    The representative western blots of β-actin, albumin, calretinin, SYPH, SYT-1, Annexin A1, ApoA4, calnexin, GNAL, GFAP, H2B, HSP90AB1 and vimentin shown as the expression levels in the retinas (A) and as the densitometric quantitative results (B). Equal amounts of protein from the control retinas and the I/R-treated retinas were loaded. Each lane represents individual retina (n = 4 or 6 in each group; *p<0.05 compared with the non-injured retinas). The error bars represent the standard error of the mean. C, Retinal I/R-induced reductions of the synaptic proteins SYPH and SYT-1. The representative western blots of synaptophysin (SYPH) and synaptotagmin-1 (SYT-1) shown as the expression levels in the retinas are seen in (A). The stained retinal sections of SYPH (B) and SYT-1 (C) are shown at 2 days after the injury. Blue color: DAPI stained nuclei as control. Red color: SYPH or SYT-1 positively stained synapses. The scale bar represents 50 µm. C, non-injured eyes; I/R, I/R-injured eyes.
    Figure Legend Snippet: The representative western blots of β-actin, albumin, calretinin, SYPH, SYT-1, Annexin A1, ApoA4, calnexin, GNAL, GFAP, H2B, HSP90AB1 and vimentin shown as the expression levels in the retinas (A) and as the densitometric quantitative results (B). Equal amounts of protein from the control retinas and the I/R-treated retinas were loaded. Each lane represents individual retina (n = 4 or 6 in each group; *p<0.05 compared with the non-injured retinas). The error bars represent the standard error of the mean. C, Retinal I/R-induced reductions of the synaptic proteins SYPH and SYT-1. The representative western blots of synaptophysin (SYPH) and synaptotagmin-1 (SYT-1) shown as the expression levels in the retinas are seen in (A). The stained retinal sections of SYPH (B) and SYT-1 (C) are shown at 2 days after the injury. Blue color: DAPI stained nuclei as control. Red color: SYPH or SYT-1 positively stained synapses. The scale bar represents 50 µm. C, non-injured eyes; I/R, I/R-injured eyes.

    Techniques Used: Western Blot, Expressing, Staining

    rabbit anti histone h2b  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit anti histone h2b
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    h2b v119 loading control antibody  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc h2b v119 loading control antibody
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    8135s  (Cell Signaling Technology Inc)


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    rabbit polyclonal anti histone h2b  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit polyclonal anti histone h2b
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    1) Product Images from "Replication gaps are a key determinant of PARP inhibitor synthetic lethality with BRCA deficiency"

    Article Title: Replication gaps are a key determinant of PARP inhibitor synthetic lethality with BRCA deficiency

    Journal: Molecular cell

    doi: 10.1016/j.molcel.2021.06.011

    KEY RESOURCES TABLE
    Figure Legend Snippet: KEY RESOURCES TABLE

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    western blot wb insulin  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc western blot wb insulin
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    histone h2b rabbit monoclonal  (Cell Signaling Technology Inc)


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    histone h2b rabbit monoclonal  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc histone h2b rabbit monoclonal
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    histone h2b  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc histone h2b
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    Cell Signaling Technology Inc rabbit anti h2b v119
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    The representative western blots of β-actin, albumin, calretinin, SYPH, SYT-1, Annexin A1, ApoA4, calnexin, GNAL, GFAP, <t>H2B,</t> HSP90AB1 and vimentin shown as the expression levels in the retinas (A) and as the densitometric quantitative results (B). Equal amounts of protein from the control retinas and the I/R-treated retinas were loaded. Each lane represents individual retina (n = 4 or 6 in each group; *p<0.05 compared with the non-injured retinas). The error bars represent the standard error of the mean. C, Retinal I/R-induced reductions of the synaptic proteins SYPH and SYT-1. The representative western blots of synaptophysin (SYPH) and synaptotagmin-1 (SYT-1) shown as the expression levels in the retinas are seen in (A). The stained retinal sections of SYPH (B) and SYT-1 (C) are shown at 2 days after the injury. Blue color: DAPI stained nuclei as control. Red color: SYPH or SYT-1 positively stained synapses. The scale bar represents 50 µm. C, non-injured eyes; I/R, I/R-injured eyes.
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    The representative western blots of β-actin, albumin, calretinin, SYPH, SYT-1, Annexin A1, ApoA4, calnexin, GNAL, GFAP, <t>H2B,</t> HSP90AB1 and vimentin shown as the expression levels in the retinas (A) and as the densitometric quantitative results (B). Equal amounts of protein from the control retinas and the I/R-treated retinas were loaded. Each lane represents individual retina (n = 4 or 6 in each group; *p<0.05 compared with the non-injured retinas). The error bars represent the standard error of the mean. C, Retinal I/R-induced reductions of the synaptic proteins SYPH and SYT-1. The representative western blots of synaptophysin (SYPH) and synaptotagmin-1 (SYT-1) shown as the expression levels in the retinas are seen in (A). The stained retinal sections of SYPH (B) and SYT-1 (C) are shown at 2 days after the injury. Blue color: DAPI stained nuclei as control. Red color: SYPH or SYT-1 positively stained synapses. The scale bar represents 50 µm. C, non-injured eyes; I/R, I/R-injured eyes.
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    The representative western blots of β-actin, albumin, calretinin, SYPH, SYT-1, Annexin A1, ApoA4, calnexin, GNAL, GFAP, <t>H2B,</t> HSP90AB1 and vimentin shown as the expression levels in the retinas (A) and as the densitometric quantitative results (B). Equal amounts of protein from the control retinas and the I/R-treated retinas were loaded. Each lane represents individual retina (n = 4 or 6 in each group; *p<0.05 compared with the non-injured retinas). The error bars represent the standard error of the mean. C, Retinal I/R-induced reductions of the synaptic proteins SYPH and SYT-1. The representative western blots of synaptophysin (SYPH) and synaptotagmin-1 (SYT-1) shown as the expression levels in the retinas are seen in (A). The stained retinal sections of SYPH (B) and SYT-1 (C) are shown at 2 days after the injury. Blue color: DAPI stained nuclei as control. Red color: SYPH or SYT-1 positively stained synapses. The scale bar represents 50 µm. C, non-injured eyes; I/R, I/R-injured eyes.
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    Image Search Results


    The representative western blots of β-actin, albumin, calretinin, SYPH, SYT-1, Annexin A1, ApoA4, calnexin, GNAL, GFAP, H2B, HSP90AB1 and vimentin shown as the expression levels in the retinas (A) and as the densitometric quantitative results (B). Equal amounts of protein from the control retinas and the I/R-treated retinas were loaded. Each lane represents individual retina (n = 4 or 6 in each group; *p<0.05 compared with the non-injured retinas). The error bars represent the standard error of the mean. C, Retinal I/R-induced reductions of the synaptic proteins SYPH and SYT-1. The representative western blots of synaptophysin (SYPH) and synaptotagmin-1 (SYT-1) shown as the expression levels in the retinas are seen in (A). The stained retinal sections of SYPH (B) and SYT-1 (C) are shown at 2 days after the injury. Blue color: DAPI stained nuclei as control. Red color: SYPH or SYT-1 positively stained synapses. The scale bar represents 50 µm. C, non-injured eyes; I/R, I/R-injured eyes.

    Journal: PLoS ONE

    Article Title: Identification of Protein Network Alterations upon Retinal Ischemia-Reperfusion Injury by Quantitative Proteomics Using a Rattus norvegicus Model

    doi: 10.1371/journal.pone.0116453

    Figure Lengend Snippet: The representative western blots of β-actin, albumin, calretinin, SYPH, SYT-1, Annexin A1, ApoA4, calnexin, GNAL, GFAP, H2B, HSP90AB1 and vimentin shown as the expression levels in the retinas (A) and as the densitometric quantitative results (B). Equal amounts of protein from the control retinas and the I/R-treated retinas were loaded. Each lane represents individual retina (n = 4 or 6 in each group; *p<0.05 compared with the non-injured retinas). The error bars represent the standard error of the mean. C, Retinal I/R-induced reductions of the synaptic proteins SYPH and SYT-1. The representative western blots of synaptophysin (SYPH) and synaptotagmin-1 (SYT-1) shown as the expression levels in the retinas are seen in (A). The stained retinal sections of SYPH (B) and SYT-1 (C) are shown at 2 days after the injury. Blue color: DAPI stained nuclei as control. Red color: SYPH or SYT-1 positively stained synapses. The scale bar represents 50 µm. C, non-injured eyes; I/R, I/R-injured eyes.

    Article Snippet: Five microgram of the proteins from in vivo and in vitro samples were fractionated by SDS-PAGE, electroblotted onto a PVDF membrane (Millipore, Billerica, MA) and probed with different antibodies: anti-Calretinin (1∶5000 dilution, #2449-1, Abcam, CA), anti-actin (1∶2000 dilution, #CW0096B, CWBIO, China), anti-Albumin (1∶10000 dilution, 16475-1-AP, Proteintech, China), anti-synaptophysin (SYPH) (1∶50000 dilution, #1485-1, Abcam, CA), anti-SYT1 (1∶10000 dilution, 14511-1-AP, Proteintech, China), anti-mTOR (1∶1000 dilution, #2983, CST, MA), anti-phospho-mTOR (Ser2448) (1∶1000 dilution, #2971, CST, MA), anti-phospho-p70 S6 Kinase (Ser371) (1∶1000 dilution, #9208, CST, MA), anti-4E-BP1 (1∶1000 dilution, #9644, CST, MA), anti-phospho-4E-BP1 (Thr37/46) (1∶1000 dilution, #2855, CST, MA), anti-GFAP (1∶5000 dilution, #7260, Abcam, CA), anti-vimentin (1∶10000 dilution, #92560, Millipore, MA), anti-ApoA4 (1∶3000 dilution, #5700, CST, MA), anti-GNAL (1∶2000 dilution, #DF4108, Affinity, OH), anti-HSP90AB1 (1∶1000 dilution, #A1087, ABclonal, MA), anti-H2B (1∶1000 dilution, #8135, CST, MA), anti-Annexin A1 (1∶2000 dilution, 21990-1-AP, Proteintech, China) and anti-calnexin (1∶5000 dilution, #2692-1, Abcam, CA).

    Techniques: Western Blot, Expressing, Staining

    KEY RESOURCES TABLE

    Journal: Molecular cell

    Article Title: Replication gaps are a key determinant of PARP inhibitor synthetic lethality with BRCA deficiency

    doi: 10.1016/j.molcel.2021.06.011

    Figure Lengend Snippet: KEY RESOURCES TABLE

    Article Snippet: Rabbit polyclonal anti-Histone H2B (V119) , Cell Signaling Technology , Cat# 8135; RRID: AB_10891053.

    Techniques: Recombinant, Electron Microscopy, Plasmid Preparation, Imaging, CCK-8 Assay, CRISPR, shRNA, Negative Control, Construct, Software, Transfection, DNA Extraction