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jmjd3 chemiluminescent assay kit  (BPS Bioscience)


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    Structured Review

    BPS Bioscience jmjd3 chemiluminescent assay kit
    Generation of AAVs that increase <t>JMJD3</t> specifically in macrophages (A) AAVs carrying an M2-trigger, JMJD3, under a macrophage-specific CD68 promoter was generated. A scramble sequence was used as a control. GFP reporters were also included in the construct for assessment of the transduction efficiency. (B) Cultured RAW264.7 cells successfully transduced with the viruses. GFP channel was shown. (C) RT-qPCR for JMJD3. (D) JMJD3 activity. ∗p < 0.05. N = 5. Scale bars are 50 μm.
    Jmjd3 Chemiluminescent Assay Kit, supplied by BPS Bioscience, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/jmjd3 chemiluminescent assay kit/product/BPS Bioscience
    Average 92 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    jmjd3 chemiluminescent assay kit - by Bioz Stars, 2025-01
    92/100 stars

    Images

    1) Product Images from "Alternative polarization of resident macrophages improves hyperglycemia-associated male infertility"

    Article Title: Alternative polarization of resident macrophages improves hyperglycemia-associated male infertility

    Journal: iScience

    doi: 10.1016/j.isci.2022.104430

    Generation of AAVs that increase JMJD3 specifically in macrophages (A) AAVs carrying an M2-trigger, JMJD3, under a macrophage-specific CD68 promoter was generated. A scramble sequence was used as a control. GFP reporters were also included in the construct for assessment of the transduction efficiency. (B) Cultured RAW264.7 cells successfully transduced with the viruses. GFP channel was shown. (C) RT-qPCR for JMJD3. (D) JMJD3 activity. ∗p < 0.05. N = 5. Scale bars are 50 μm.
    Figure Legend Snippet: Generation of AAVs that increase JMJD3 specifically in macrophages (A) AAVs carrying an M2-trigger, JMJD3, under a macrophage-specific CD68 promoter was generated. A scramble sequence was used as a control. GFP reporters were also included in the construct for assessment of the transduction efficiency. (B) Cultured RAW264.7 cells successfully transduced with the viruses. GFP channel was shown. (C) RT-qPCR for JMJD3. (D) JMJD3 activity. ∗p < 0.05. N = 5. Scale bars are 50 μm.

    Techniques Used: Generated, Sequencing, Construct, Transduction, Cell Culture, Quantitative RT-PCR, Activity Assay

    Orthotopic injection of AAVs in the testis does not alter diabetes (A) Schematic of the study: we assigned male mice into four groups of five each. Group 1: mice only received an intraperitoneal injection of saline (control for STZ). Group 2: mice only received an intraperitoneal injection of STZ. Group 3: mice received an intraperitoneal injection of STZ and an orthotopic injection of AAVs carrying control Scr into the testis one week after STZ. Group 4: mice received an intraperitoneal injection of STZ and an orthotopic injection of AAVs carrying control JMJD3 into the testis one week after STZ. Mice were examined 12 weeks after treatment. (B) Fasting blood glucose. (C) Serum insulin. (D) Beta-cell mass at sacrifice. (E) Representative immunofluorescent images for insulin in mouse pancreas. ∗p < 0.05. NS: non-significant. N = 5. Scale bars are 100 μm.
    Figure Legend Snippet: Orthotopic injection of AAVs in the testis does not alter diabetes (A) Schematic of the study: we assigned male mice into four groups of five each. Group 1: mice only received an intraperitoneal injection of saline (control for STZ). Group 2: mice only received an intraperitoneal injection of STZ. Group 3: mice received an intraperitoneal injection of STZ and an orthotopic injection of AAVs carrying control Scr into the testis one week after STZ. Group 4: mice received an intraperitoneal injection of STZ and an orthotopic injection of AAVs carrying control JMJD3 into the testis one week after STZ. Mice were examined 12 weeks after treatment. (B) Fasting blood glucose. (C) Serum insulin. (D) Beta-cell mass at sacrifice. (E) Representative immunofluorescent images for insulin in mouse pancreas. ∗p < 0.05. NS: non-significant. N = 5. Scale bars are 100 μm.

    Techniques Used: Injection

    JMJD3 expression in testicular macrophages improves mating capability of diabetic male mice At the beginning of the 12 weeks after AAV injection (or the beginning of the 13 weeks after STZ injection; or one week before sacrifice), each male C57BL/6 mouse from four groups was caged with four age-matched untreated female C57BL/6 mice for one week before they were removed from the females for final analysis followed by sacrifice. (A) Vaginal mucous pups in females. (B) Pregnancies per male. (C) Litter sizes for successful pregnancies. ∗p < 0.05. NS: non-significant. N = 5.
    Figure Legend Snippet: JMJD3 expression in testicular macrophages improves mating capability of diabetic male mice At the beginning of the 12 weeks after AAV injection (or the beginning of the 13 weeks after STZ injection; or one week before sacrifice), each male C57BL/6 mouse from four groups was caged with four age-matched untreated female C57BL/6 mice for one week before they were removed from the females for final analysis followed by sacrifice. (A) Vaginal mucous pups in females. (B) Pregnancies per male. (C) Litter sizes for successful pregnancies. ∗p < 0.05. NS: non-significant. N = 5.

    Techniques Used: Expressing, Injection

    JMJD3 expression in testicular macrophages improves sperm motility Computer-assisted sperm motility analysis was performed. (A) the motile percentage of sperms. (B and C) curvilinear velocity (C) straight line velocity (C). ∗p < 0.05. NS, non-significant. N = 5.
    Figure Legend Snippet: JMJD3 expression in testicular macrophages improves sperm motility Computer-assisted sperm motility analysis was performed. (A) the motile percentage of sperms. (B and C) curvilinear velocity (C) straight line velocity (C). ∗p < 0.05. NS, non-significant. N = 5.

    Techniques Used: Expressing

    JMJD3 expression in testicular macrophages increases testosterone (A–D) The levels of LH (A), FSH (B), and testosterone (C) in serum and the levels of testosterone in testis (D). ∗p < 0.05. NS: non-significant. N = 5.
    Figure Legend Snippet: JMJD3 expression in testicular macrophages increases testosterone (A–D) The levels of LH (A), FSH (B), and testosterone (C) in serum and the levels of testosterone in testis (D). ∗p < 0.05. NS: non-significant. N = 5.

    Techniques Used: Expressing

    JMJD3 repolarizes testicular macrophages back to M2-polarized phenotype (A) The digested testicle cells were subjected to CD68 and GFP double FACS, showing that GFP was exclusively detected in CD68 + cell fraction. (B) RT-qPCR for GFP in testis, blood, liver, lung, and kidney in mice. (C and D) Testicular macrophages were isolated and subjected to flow cytometry. (C) Quantification for % CD163 + cells in total CD68 + cells. (D) Representative flow charts for CD68 and CD163. (E) RT-qPCR for M2 markers (CD206 and Arginase 1 (ARG1)) and M1 markers (iNOS, IL-6, and TNFα) in testicular CD68 + macrophages. ∗p < 0.05. NS, non-significant. N = 5.
    Figure Legend Snippet: JMJD3 repolarizes testicular macrophages back to M2-polarized phenotype (A) The digested testicle cells were subjected to CD68 and GFP double FACS, showing that GFP was exclusively detected in CD68 + cell fraction. (B) RT-qPCR for GFP in testis, blood, liver, lung, and kidney in mice. (C and D) Testicular macrophages were isolated and subjected to flow cytometry. (C) Quantification for % CD163 + cells in total CD68 + cells. (D) Representative flow charts for CD68 and CD163. (E) RT-qPCR for M2 markers (CD206 and Arginase 1 (ARG1)) and M1 markers (iNOS, IL-6, and TNFα) in testicular CD68 + macrophages. ∗p < 0.05. NS, non-significant. N = 5.

    Techniques Used: Quantitative RT-PCR, Isolation, Flow Cytometry


    Figure Legend Snippet:

    Techniques Used: Recombinant, Plasmid Preparation, Software



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    Generation of AAVs that increase <t>JMJD3</t> specifically in macrophages (A) AAVs carrying an M2-trigger, JMJD3, under a macrophage-specific CD68 promoter was generated. A scramble sequence was used as a control. GFP reporters were also included in the construct for assessment of the transduction efficiency. (B) Cultured RAW264.7 cells successfully transduced with the viruses. GFP channel was shown. (C) RT-qPCR for JMJD3. (D) JMJD3 activity. ∗p < 0.05. N = 5. Scale bars are 50 μm.
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    Reversible, oxygen-dependent global changes of H3K4me3 and H3K27me3 levels. a Immunoblot detection (IB) of epigenetic changes (H3K4me3 and H3K27me3) in MCF7 cells; loading control: total H3 (H3); lower panel quantification. b Ability of recombinant <t>JMJD3</t> to demethylate H3K27me3 peptide in vitro was determined at 0.02, 0.2, 1, 5 and 21% (ambient) partial O 2 pressure; EDTA was used as a negative control as it blocks JMJD3 activity. Number of peaks for H3K4me3 ( c ) and H3K27me3 ( d ) significantly above background level ( p < 0.05) at different time points under hypoxic conditions ( t = 8, t = 24 h) and after reoxygenation ( t = +8 h). Bottom panels to c and d : representative gene tracks of loci displaying H3K4me3 gain ( ATP2A3 , GPRC5B ) or H3K27me3 gain ( CYP1B1 , OPRL1 ); diamond symbol indicates direction of gene transcription
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    Image Search Results


    Generation of AAVs that increase JMJD3 specifically in macrophages (A) AAVs carrying an M2-trigger, JMJD3, under a macrophage-specific CD68 promoter was generated. A scramble sequence was used as a control. GFP reporters were also included in the construct for assessment of the transduction efficiency. (B) Cultured RAW264.7 cells successfully transduced with the viruses. GFP channel was shown. (C) RT-qPCR for JMJD3. (D) JMJD3 activity. ∗p < 0.05. N = 5. Scale bars are 50 μm.

    Journal: iScience

    Article Title: Alternative polarization of resident macrophages improves hyperglycemia-associated male infertility

    doi: 10.1016/j.isci.2022.104430

    Figure Lengend Snippet: Generation of AAVs that increase JMJD3 specifically in macrophages (A) AAVs carrying an M2-trigger, JMJD3, under a macrophage-specific CD68 promoter was generated. A scramble sequence was used as a control. GFP reporters were also included in the construct for assessment of the transduction efficiency. (B) Cultured RAW264.7 cells successfully transduced with the viruses. GFP channel was shown. (C) RT-qPCR for JMJD3. (D) JMJD3 activity. ∗p < 0.05. N = 5. Scale bars are 50 μm.

    Article Snippet: JMJD3 chemiluminescent Assay Kit , BPS Bioscience , #50406.

    Techniques: Generated, Sequencing, Construct, Transduction, Cell Culture, Quantitative RT-PCR, Activity Assay

    Orthotopic injection of AAVs in the testis does not alter diabetes (A) Schematic of the study: we assigned male mice into four groups of five each. Group 1: mice only received an intraperitoneal injection of saline (control for STZ). Group 2: mice only received an intraperitoneal injection of STZ. Group 3: mice received an intraperitoneal injection of STZ and an orthotopic injection of AAVs carrying control Scr into the testis one week after STZ. Group 4: mice received an intraperitoneal injection of STZ and an orthotopic injection of AAVs carrying control JMJD3 into the testis one week after STZ. Mice were examined 12 weeks after treatment. (B) Fasting blood glucose. (C) Serum insulin. (D) Beta-cell mass at sacrifice. (E) Representative immunofluorescent images for insulin in mouse pancreas. ∗p < 0.05. NS: non-significant. N = 5. Scale bars are 100 μm.

    Journal: iScience

    Article Title: Alternative polarization of resident macrophages improves hyperglycemia-associated male infertility

    doi: 10.1016/j.isci.2022.104430

    Figure Lengend Snippet: Orthotopic injection of AAVs in the testis does not alter diabetes (A) Schematic of the study: we assigned male mice into four groups of five each. Group 1: mice only received an intraperitoneal injection of saline (control for STZ). Group 2: mice only received an intraperitoneal injection of STZ. Group 3: mice received an intraperitoneal injection of STZ and an orthotopic injection of AAVs carrying control Scr into the testis one week after STZ. Group 4: mice received an intraperitoneal injection of STZ and an orthotopic injection of AAVs carrying control JMJD3 into the testis one week after STZ. Mice were examined 12 weeks after treatment. (B) Fasting blood glucose. (C) Serum insulin. (D) Beta-cell mass at sacrifice. (E) Representative immunofluorescent images for insulin in mouse pancreas. ∗p < 0.05. NS: non-significant. N = 5. Scale bars are 100 μm.

    Article Snippet: JMJD3 chemiluminescent Assay Kit , BPS Bioscience , #50406.

    Techniques: Injection

    JMJD3 expression in testicular macrophages improves mating capability of diabetic male mice At the beginning of the 12 weeks after AAV injection (or the beginning of the 13 weeks after STZ injection; or one week before sacrifice), each male C57BL/6 mouse from four groups was caged with four age-matched untreated female C57BL/6 mice for one week before they were removed from the females for final analysis followed by sacrifice. (A) Vaginal mucous pups in females. (B) Pregnancies per male. (C) Litter sizes for successful pregnancies. ∗p < 0.05. NS: non-significant. N = 5.

    Journal: iScience

    Article Title: Alternative polarization of resident macrophages improves hyperglycemia-associated male infertility

    doi: 10.1016/j.isci.2022.104430

    Figure Lengend Snippet: JMJD3 expression in testicular macrophages improves mating capability of diabetic male mice At the beginning of the 12 weeks after AAV injection (or the beginning of the 13 weeks after STZ injection; or one week before sacrifice), each male C57BL/6 mouse from four groups was caged with four age-matched untreated female C57BL/6 mice for one week before they were removed from the females for final analysis followed by sacrifice. (A) Vaginal mucous pups in females. (B) Pregnancies per male. (C) Litter sizes for successful pregnancies. ∗p < 0.05. NS: non-significant. N = 5.

    Article Snippet: JMJD3 chemiluminescent Assay Kit , BPS Bioscience , #50406.

    Techniques: Expressing, Injection

    JMJD3 expression in testicular macrophages improves sperm motility Computer-assisted sperm motility analysis was performed. (A) the motile percentage of sperms. (B and C) curvilinear velocity (C) straight line velocity (C). ∗p < 0.05. NS, non-significant. N = 5.

    Journal: iScience

    Article Title: Alternative polarization of resident macrophages improves hyperglycemia-associated male infertility

    doi: 10.1016/j.isci.2022.104430

    Figure Lengend Snippet: JMJD3 expression in testicular macrophages improves sperm motility Computer-assisted sperm motility analysis was performed. (A) the motile percentage of sperms. (B and C) curvilinear velocity (C) straight line velocity (C). ∗p < 0.05. NS, non-significant. N = 5.

    Article Snippet: JMJD3 chemiluminescent Assay Kit , BPS Bioscience , #50406.

    Techniques: Expressing

    JMJD3 expression in testicular macrophages increases testosterone (A–D) The levels of LH (A), FSH (B), and testosterone (C) in serum and the levels of testosterone in testis (D). ∗p < 0.05. NS: non-significant. N = 5.

    Journal: iScience

    Article Title: Alternative polarization of resident macrophages improves hyperglycemia-associated male infertility

    doi: 10.1016/j.isci.2022.104430

    Figure Lengend Snippet: JMJD3 expression in testicular macrophages increases testosterone (A–D) The levels of LH (A), FSH (B), and testosterone (C) in serum and the levels of testosterone in testis (D). ∗p < 0.05. NS: non-significant. N = 5.

    Article Snippet: JMJD3 chemiluminescent Assay Kit , BPS Bioscience , #50406.

    Techniques: Expressing

    JMJD3 repolarizes testicular macrophages back to M2-polarized phenotype (A) The digested testicle cells were subjected to CD68 and GFP double FACS, showing that GFP was exclusively detected in CD68 + cell fraction. (B) RT-qPCR for GFP in testis, blood, liver, lung, and kidney in mice. (C and D) Testicular macrophages were isolated and subjected to flow cytometry. (C) Quantification for % CD163 + cells in total CD68 + cells. (D) Representative flow charts for CD68 and CD163. (E) RT-qPCR for M2 markers (CD206 and Arginase 1 (ARG1)) and M1 markers (iNOS, IL-6, and TNFα) in testicular CD68 + macrophages. ∗p < 0.05. NS, non-significant. N = 5.

    Journal: iScience

    Article Title: Alternative polarization of resident macrophages improves hyperglycemia-associated male infertility

    doi: 10.1016/j.isci.2022.104430

    Figure Lengend Snippet: JMJD3 repolarizes testicular macrophages back to M2-polarized phenotype (A) The digested testicle cells were subjected to CD68 and GFP double FACS, showing that GFP was exclusively detected in CD68 + cell fraction. (B) RT-qPCR for GFP in testis, blood, liver, lung, and kidney in mice. (C and D) Testicular macrophages were isolated and subjected to flow cytometry. (C) Quantification for % CD163 + cells in total CD68 + cells. (D) Representative flow charts for CD68 and CD163. (E) RT-qPCR for M2 markers (CD206 and Arginase 1 (ARG1)) and M1 markers (iNOS, IL-6, and TNFα) in testicular CD68 + macrophages. ∗p < 0.05. NS, non-significant. N = 5.

    Article Snippet: JMJD3 chemiluminescent Assay Kit , BPS Bioscience , #50406.

    Techniques: Quantitative RT-PCR, Isolation, Flow Cytometry

    Journal: iScience

    Article Title: Alternative polarization of resident macrophages improves hyperglycemia-associated male infertility

    doi: 10.1016/j.isci.2022.104430

    Figure Lengend Snippet:

    Article Snippet: JMJD3 chemiluminescent Assay Kit , BPS Bioscience , #50406.

    Techniques: Recombinant, Plasmid Preparation, Software

    Reversible, oxygen-dependent global changes of H3K4me3 and H3K27me3 levels. a Immunoblot detection (IB) of epigenetic changes (H3K4me3 and H3K27me3) in MCF7 cells; loading control: total H3 (H3); lower panel quantification. b Ability of recombinant JMJD3 to demethylate H3K27me3 peptide in vitro was determined at 0.02, 0.2, 1, 5 and 21% (ambient) partial O 2 pressure; EDTA was used as a negative control as it blocks JMJD3 activity. Number of peaks for H3K4me3 ( c ) and H3K27me3 ( d ) significantly above background level ( p < 0.05) at different time points under hypoxic conditions ( t = 8, t = 24 h) and after reoxygenation ( t = +8 h). Bottom panels to c and d : representative gene tracks of loci displaying H3K4me3 gain ( ATP2A3 , GPRC5B ) or H3K27me3 gain ( CYP1B1 , OPRL1 ); diamond symbol indicates direction of gene transcription

    Journal: Epigenetics & Chromatin

    Article Title: Hypoxia increases genome-wide bivalent epigenetic marking by specific gain of H3K27me3

    doi: 10.1186/s13072-016-0086-0

    Figure Lengend Snippet: Reversible, oxygen-dependent global changes of H3K4me3 and H3K27me3 levels. a Immunoblot detection (IB) of epigenetic changes (H3K4me3 and H3K27me3) in MCF7 cells; loading control: total H3 (H3); lower panel quantification. b Ability of recombinant JMJD3 to demethylate H3K27me3 peptide in vitro was determined at 0.02, 0.2, 1, 5 and 21% (ambient) partial O 2 pressure; EDTA was used as a negative control as it blocks JMJD3 activity. Number of peaks for H3K4me3 ( c ) and H3K27me3 ( d ) significantly above background level ( p < 0.05) at different time points under hypoxic conditions ( t = 8, t = 24 h) and after reoxygenation ( t = +8 h). Bottom panels to c and d : representative gene tracks of loci displaying H3K4me3 gain ( ATP2A3 , GPRC5B ) or H3K27me3 gain ( CYP1B1 , OPRL1 ); diamond symbol indicates direction of gene transcription

    Article Snippet: KDM6B (JMJD3) activity was measured using the JMJD3 Chemiluminescent Assay Kit (Tebu-Bio, The Netherlands) according to the manufacturers’ instructions.

    Techniques: Western Blot, Recombinant, In Vitro, Negative Control, Activity Assay