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adamts1 antibody  (NSJ Bioreagents)


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    Structured Review

    NSJ Bioreagents adamts1 antibody
    Primers Used for Quantitative PCR.
    Adamts1 Antibody, supplied by NSJ Bioreagents, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/adamts1 antibody/product/NSJ Bioreagents
    Average 93 stars, based on 1 article reviews
    adamts1 antibody - by Bioz Stars, 2026-01
    93/100 stars

    Images

    1) Product Images from "Protease expression in the human and rat cumulus–oocyte complex during the periovulatory period: a role in cumulus–oocyte complex migration "

    Article Title: Protease expression in the human and rat cumulus–oocyte complex during the periovulatory period: a role in cumulus–oocyte complex migration

    Journal: Biology of Reproduction

    doi: 10.1093/biolre/ioae108

    Primers Used for Quantitative PCR.
    Figure Legend Snippet: Primers Used for Quantitative PCR.

    Techniques Used:

    Expression profile of proteases and protease inhibitors in the rat COC during the periovulatory period in vivo. Depicted is the mRNA expression profile of the proteases Mmp2 (A), Mmp14 (B), Mmp13 (C), Mmp16 (D), Adamts1 (E), and Mmp9 (F) and the protease inhibitors Timp1 (G), Timp3 (H), and Serpine1 (I) in the COC collected from PMSG-primed immature rats at 0 (48 h after PMSG), or 4, 8, 12, and 24 h after administration of hCG. Relative levels of mRNA were normalized to Rpl32 in each sample and expressed as a fold change relative to the 0 h ( n = 4/time point). Different superscripts indicate significant changes ( P < 0.05) in mRNA levels. Representative western blots of MMP13 (inset, upper panel C), ADAMTS1 (inset, upper panel E), and BACT proteins as loading control at 0, 12, and 24 h.
    Figure Legend Snippet: Expression profile of proteases and protease inhibitors in the rat COC during the periovulatory period in vivo. Depicted is the mRNA expression profile of the proteases Mmp2 (A), Mmp14 (B), Mmp13 (C), Mmp16 (D), Adamts1 (E), and Mmp9 (F) and the protease inhibitors Timp1 (G), Timp3 (H), and Serpine1 (I) in the COC collected from PMSG-primed immature rats at 0 (48 h after PMSG), or 4, 8, 12, and 24 h after administration of hCG. Relative levels of mRNA were normalized to Rpl32 in each sample and expressed as a fold change relative to the 0 h ( n = 4/time point). Different superscripts indicate significant changes ( P < 0.05) in mRNA levels. Representative western blots of MMP13 (inset, upper panel C), ADAMTS1 (inset, upper panel E), and BACT proteins as loading control at 0, 12, and 24 h.

    Techniques Used: Expressing, In Vivo, Western Blot, Control

    Expression profile of proteases and their inhibitors in rat granulosa cells and COCs in vivo. Depicted is the mRNA expression profile of the proteases Mmp2 (A), Mmp9 (B), Mmp13 (C), Mmp14 (D), Mmp16 (E), Adamts1 (F), and protease inhibitors Timp1 (G) and Timp3 (H) in granulosa and cumulus cells collected from the same animal at 12 h post hCG administration. Relative levels of mRNA were normalized to Rpl32 in each sample and expressed as a fold change relative to granulosa cells ( n = 5). * indicates significant statistical difference ( P < 0.05) in mRNA levels as determined by Student’s t -test.
    Figure Legend Snippet: Expression profile of proteases and their inhibitors in rat granulosa cells and COCs in vivo. Depicted is the mRNA expression profile of the proteases Mmp2 (A), Mmp9 (B), Mmp13 (C), Mmp14 (D), Mmp16 (E), Adamts1 (F), and protease inhibitors Timp1 (G) and Timp3 (H) in granulosa and cumulus cells collected from the same animal at 12 h post hCG administration. Relative levels of mRNA were normalized to Rpl32 in each sample and expressed as a fold change relative to granulosa cells ( n = 5). * indicates significant statistical difference ( P < 0.05) in mRNA levels as determined by Student’s t -test.

    Techniques Used: Expressing, In Vivo

    Expression profile of the proteases and their inhibitors in human granulosa and cumulus cells in vivo. Depicted is the expression profile of the proteases MMP1 (A), MMP2 (B), MMP9 (C), MMP14 (D), MMP16 (E), and ADAMTS1 (F), and protease inhibitors TIMP1 (G) and TIMP3 (H) in granulosa and cumulus cells collected 36 h post hCG administration from women undergoing IVF. Relative levels of mRNA were normalized to GAPDH in each sample and expressed as a fold change relative to the expression in granulosa cells ( n = 4–8). Granulosa and cumulus cell expression were compared from the same patient. * indicates significant statistical difference ( P < 0.05) in mRNA levels as determined by Student’s t -test.
    Figure Legend Snippet: Expression profile of the proteases and their inhibitors in human granulosa and cumulus cells in vivo. Depicted is the expression profile of the proteases MMP1 (A), MMP2 (B), MMP9 (C), MMP14 (D), MMP16 (E), and ADAMTS1 (F), and protease inhibitors TIMP1 (G) and TIMP3 (H) in granulosa and cumulus cells collected 36 h post hCG administration from women undergoing IVF. Relative levels of mRNA were normalized to GAPDH in each sample and expressed as a fold change relative to the expression in granulosa cells ( n = 4–8). Granulosa and cumulus cell expression were compared from the same patient. * indicates significant statistical difference ( P < 0.05) in mRNA levels as determined by Student’s t -test.

    Techniques Used: Expressing, In Vivo



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    NSJ Bioreagents adamts1 antibody
    Primers Used for Quantitative PCR.
    Adamts1 Antibody, supplied by NSJ Bioreagents, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/adamts1 antibody/product/NSJ Bioreagents
    Average 93 stars, based on 1 article reviews
    adamts1 antibody - by Bioz Stars, 2026-01
    93/100 stars
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    Primers Used for Quantitative PCR.

    Journal: Biology of Reproduction

    Article Title: Protease expression in the human and rat cumulus–oocyte complex during the periovulatory period: a role in cumulus–oocyte complex migration

    doi: 10.1093/biolre/ioae108

    Figure Lengend Snippet: Primers Used for Quantitative PCR.

    Article Snippet: Membranes were blocked for 1 h at room temperature in TBST (25 mM Tris, 137 mM NaCl, 2.7 mM KCl, and 0.05% TWEEN-20) containing 5% low-fat milk and then incubated overnight at 4°C with 1:1000 anti-MMP13 antibody (Abcam Cat# ab39012, RRID:AB_776416), 1:1000 ADAMTS1 antibody (NSJBio Cat#R31182, RRID:AB_3075893), and 1:1000 rabbit anti-BACT (13E5; Cell Signaling Technology Cat# 4970, RRID:AB_2223172).

    Techniques:

    Expression profile of proteases and protease inhibitors in the rat COC during the periovulatory period in vivo. Depicted is the mRNA expression profile of the proteases Mmp2 (A), Mmp14 (B), Mmp13 (C), Mmp16 (D), Adamts1 (E), and Mmp9 (F) and the protease inhibitors Timp1 (G), Timp3 (H), and Serpine1 (I) in the COC collected from PMSG-primed immature rats at 0 (48 h after PMSG), or 4, 8, 12, and 24 h after administration of hCG. Relative levels of mRNA were normalized to Rpl32 in each sample and expressed as a fold change relative to the 0 h ( n = 4/time point). Different superscripts indicate significant changes ( P < 0.05) in mRNA levels. Representative western blots of MMP13 (inset, upper panel C), ADAMTS1 (inset, upper panel E), and BACT proteins as loading control at 0, 12, and 24 h.

    Journal: Biology of Reproduction

    Article Title: Protease expression in the human and rat cumulus–oocyte complex during the periovulatory period: a role in cumulus–oocyte complex migration

    doi: 10.1093/biolre/ioae108

    Figure Lengend Snippet: Expression profile of proteases and protease inhibitors in the rat COC during the periovulatory period in vivo. Depicted is the mRNA expression profile of the proteases Mmp2 (A), Mmp14 (B), Mmp13 (C), Mmp16 (D), Adamts1 (E), and Mmp9 (F) and the protease inhibitors Timp1 (G), Timp3 (H), and Serpine1 (I) in the COC collected from PMSG-primed immature rats at 0 (48 h after PMSG), or 4, 8, 12, and 24 h after administration of hCG. Relative levels of mRNA were normalized to Rpl32 in each sample and expressed as a fold change relative to the 0 h ( n = 4/time point). Different superscripts indicate significant changes ( P < 0.05) in mRNA levels. Representative western blots of MMP13 (inset, upper panel C), ADAMTS1 (inset, upper panel E), and BACT proteins as loading control at 0, 12, and 24 h.

    Article Snippet: Membranes were blocked for 1 h at room temperature in TBST (25 mM Tris, 137 mM NaCl, 2.7 mM KCl, and 0.05% TWEEN-20) containing 5% low-fat milk and then incubated overnight at 4°C with 1:1000 anti-MMP13 antibody (Abcam Cat# ab39012, RRID:AB_776416), 1:1000 ADAMTS1 antibody (NSJBio Cat#R31182, RRID:AB_3075893), and 1:1000 rabbit anti-BACT (13E5; Cell Signaling Technology Cat# 4970, RRID:AB_2223172).

    Techniques: Expressing, In Vivo, Western Blot, Control

    Expression profile of proteases and their inhibitors in rat granulosa cells and COCs in vivo. Depicted is the mRNA expression profile of the proteases Mmp2 (A), Mmp9 (B), Mmp13 (C), Mmp14 (D), Mmp16 (E), Adamts1 (F), and protease inhibitors Timp1 (G) and Timp3 (H) in granulosa and cumulus cells collected from the same animal at 12 h post hCG administration. Relative levels of mRNA were normalized to Rpl32 in each sample and expressed as a fold change relative to granulosa cells ( n = 5). * indicates significant statistical difference ( P < 0.05) in mRNA levels as determined by Student’s t -test.

    Journal: Biology of Reproduction

    Article Title: Protease expression in the human and rat cumulus–oocyte complex during the periovulatory period: a role in cumulus–oocyte complex migration

    doi: 10.1093/biolre/ioae108

    Figure Lengend Snippet: Expression profile of proteases and their inhibitors in rat granulosa cells and COCs in vivo. Depicted is the mRNA expression profile of the proteases Mmp2 (A), Mmp9 (B), Mmp13 (C), Mmp14 (D), Mmp16 (E), Adamts1 (F), and protease inhibitors Timp1 (G) and Timp3 (H) in granulosa and cumulus cells collected from the same animal at 12 h post hCG administration. Relative levels of mRNA were normalized to Rpl32 in each sample and expressed as a fold change relative to granulosa cells ( n = 5). * indicates significant statistical difference ( P < 0.05) in mRNA levels as determined by Student’s t -test.

    Article Snippet: Membranes were blocked for 1 h at room temperature in TBST (25 mM Tris, 137 mM NaCl, 2.7 mM KCl, and 0.05% TWEEN-20) containing 5% low-fat milk and then incubated overnight at 4°C with 1:1000 anti-MMP13 antibody (Abcam Cat# ab39012, RRID:AB_776416), 1:1000 ADAMTS1 antibody (NSJBio Cat#R31182, RRID:AB_3075893), and 1:1000 rabbit anti-BACT (13E5; Cell Signaling Technology Cat# 4970, RRID:AB_2223172).

    Techniques: Expressing, In Vivo

    Expression profile of the proteases and their inhibitors in human granulosa and cumulus cells in vivo. Depicted is the expression profile of the proteases MMP1 (A), MMP2 (B), MMP9 (C), MMP14 (D), MMP16 (E), and ADAMTS1 (F), and protease inhibitors TIMP1 (G) and TIMP3 (H) in granulosa and cumulus cells collected 36 h post hCG administration from women undergoing IVF. Relative levels of mRNA were normalized to GAPDH in each sample and expressed as a fold change relative to the expression in granulosa cells ( n = 4–8). Granulosa and cumulus cell expression were compared from the same patient. * indicates significant statistical difference ( P < 0.05) in mRNA levels as determined by Student’s t -test.

    Journal: Biology of Reproduction

    Article Title: Protease expression in the human and rat cumulus–oocyte complex during the periovulatory period: a role in cumulus–oocyte complex migration

    doi: 10.1093/biolre/ioae108

    Figure Lengend Snippet: Expression profile of the proteases and their inhibitors in human granulosa and cumulus cells in vivo. Depicted is the expression profile of the proteases MMP1 (A), MMP2 (B), MMP9 (C), MMP14 (D), MMP16 (E), and ADAMTS1 (F), and protease inhibitors TIMP1 (G) and TIMP3 (H) in granulosa and cumulus cells collected 36 h post hCG administration from women undergoing IVF. Relative levels of mRNA were normalized to GAPDH in each sample and expressed as a fold change relative to the expression in granulosa cells ( n = 4–8). Granulosa and cumulus cell expression were compared from the same patient. * indicates significant statistical difference ( P < 0.05) in mRNA levels as determined by Student’s t -test.

    Article Snippet: Membranes were blocked for 1 h at room temperature in TBST (25 mM Tris, 137 mM NaCl, 2.7 mM KCl, and 0.05% TWEEN-20) containing 5% low-fat milk and then incubated overnight at 4°C with 1:1000 anti-MMP13 antibody (Abcam Cat# ab39012, RRID:AB_776416), 1:1000 ADAMTS1 antibody (NSJBio Cat#R31182, RRID:AB_3075893), and 1:1000 rabbit anti-BACT (13E5; Cell Signaling Technology Cat# 4970, RRID:AB_2223172).

    Techniques: Expressing, In Vivo