rabbit anti mmp 2 pab Search Results


94
Bioss anti mmp2
Relative mRNA expression rates of genes in chondrocytes by PCR. (A) SELE. (B) <t>MMP2.</t> (C) COL1. * P < 0.05, ** P < 0.01, *** P < 0.001 versus the IL-1β group.
Anti Mmp2, supplied by Bioss, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bioss rabbit anti human polyclonal antibody against mmp 2
Girdin silencing inhibits the expression and activity of <t>MMP-2</t> and MMP-9. (A and B) Changes in the mRNA levels of MMP-2 and MMP-9 were measured using reverse transcription-quantitative polymerase chain reaction following transfection. The relative mRNA expression levels were calculated using the 2 −ΔΔCt method. (C and D) Following transfection, changes in the protein levels of MMP-2 and MMP-9 were detected using western blot analysis. (E and F) Following transfection, gelatin zymography was performed to detect changes in the activities of MMP-2 and MMP-9. Each experiment was repeated three times. The experimental results are presented as the mean ± standard deviation. ** P<0.01, compared with the NC group. shRNA, short hairpin RNA; NC, negative control.
Rabbit Anti Human Polyclonal Antibody Against Mmp 2, supplied by Bioss, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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95
R&D Systems goat anti mouse mmp 2
Girdin silencing inhibits the expression and activity of <t>MMP-2</t> and MMP-9. (A and B) Changes in the mRNA levels of MMP-2 and MMP-9 were measured using reverse transcription-quantitative polymerase chain reaction following transfection. The relative mRNA expression levels were calculated using the 2 −ΔΔCt method. (C and D) Following transfection, changes in the protein levels of MMP-2 and MMP-9 were detected using western blot analysis. (E and F) Following transfection, gelatin zymography was performed to detect changes in the activities of MMP-2 and MMP-9. Each experiment was repeated three times. The experimental results are presented as the mean ± standard deviation. ** P<0.01, compared with the NC group. shRNA, short hairpin RNA; NC, negative control.
Goat Anti Mouse Mmp 2, supplied by R&D Systems, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 95 stars, based on 1 article reviews
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90
Torrey Pines Biolabs rabbit polyclonal anti-mmp2
Girdin silencing inhibits the expression and activity of <t>MMP-2</t> and MMP-9. (A and B) Changes in the mRNA levels of MMP-2 and MMP-9 were measured using reverse transcription-quantitative polymerase chain reaction following transfection. The relative mRNA expression levels were calculated using the 2 −ΔΔCt method. (C and D) Following transfection, changes in the protein levels of MMP-2 and MMP-9 were detected using western blot analysis. (E and F) Following transfection, gelatin zymography was performed to detect changes in the activities of MMP-2 and MMP-9. Each experiment was repeated three times. The experimental results are presented as the mean ± standard deviation. ** P<0.01, compared with the NC group. shRNA, short hairpin RNA; NC, negative control.
Rabbit Polyclonal Anti Mmp2, supplied by Torrey Pines Biolabs, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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96
Proteintech rabbit polyclonal anti gr
Girdin silencing inhibits the expression and activity of <t>MMP-2</t> and MMP-9. (A and B) Changes in the mRNA levels of MMP-2 and MMP-9 were measured using reverse transcription-quantitative polymerase chain reaction following transfection. The relative mRNA expression levels were calculated using the 2 −ΔΔCt method. (C and D) Following transfection, changes in the protein levels of MMP-2 and MMP-9 were detected using western blot analysis. (E and F) Following transfection, gelatin zymography was performed to detect changes in the activities of MMP-2 and MMP-9. Each experiment was repeated three times. The experimental results are presented as the mean ± standard deviation. ** P<0.01, compared with the NC group. shRNA, short hairpin RNA; NC, negative control.
Rabbit Polyclonal Anti Gr, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+mmp+2+pab/MMP2+Polyclonal+antibody/10__1172_slash_jci96138-331-33-36
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93
Novus Biologicals rabbit polyclonal anti mmp 2
Girdin silencing inhibits the expression and activity of <t>MMP-2</t> and MMP-9. (A and B) Changes in the mRNA levels of MMP-2 and MMP-9 were measured using reverse transcription-quantitative polymerase chain reaction following transfection. The relative mRNA expression levels were calculated using the 2 −ΔΔCt method. (C and D) Following transfection, changes in the protein levels of MMP-2 and MMP-9 were detected using western blot analysis. (E and F) Following transfection, gelatin zymography was performed to detect changes in the activities of MMP-2 and MMP-9. Each experiment was repeated three times. The experimental results are presented as the mean ± standard deviation. ** P<0.01, compared with the NC group. shRNA, short hairpin RNA; NC, negative control.
Rabbit Polyclonal Anti Mmp 2, supplied by Novus Biologicals, 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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96
Cell Signaling Technology Inc anti mmp 2
Girdin silencing inhibits the expression and activity of <t>MMP-2</t> and MMP-9. (A and B) Changes in the mRNA levels of MMP-2 and MMP-9 were measured using reverse transcription-quantitative polymerase chain reaction following transfection. The relative mRNA expression levels were calculated using the 2 −ΔΔCt method. (C and D) Following transfection, changes in the protein levels of MMP-2 and MMP-9 were detected using western blot analysis. (E and F) Following transfection, gelatin zymography was performed to detect changes in the activities of MMP-2 and MMP-9. Each experiment was repeated three times. The experimental results are presented as the mean ± standard deviation. ** P<0.01, compared with the NC group. shRNA, short hairpin RNA; NC, negative control.
Anti Mmp 2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+mmp+2+pab/MMP-2+Rabbit+mAb/pmc05601719-109-44-52
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93
Cusabio rabbit anti mmp2
Girdin silencing inhibits the expression and activity of <t>MMP-2</t> and MMP-9. (A and B) Changes in the mRNA levels of MMP-2 and MMP-9 were measured using reverse transcription-quantitative polymerase chain reaction following transfection. The relative mRNA expression levels were calculated using the 2 −ΔΔCt method. (C and D) Following transfection, changes in the protein levels of MMP-2 and MMP-9 were detected using western blot analysis. (E and F) Following transfection, gelatin zymography was performed to detect changes in the activities of MMP-2 and MMP-9. Each experiment was repeated three times. The experimental results are presented as the mean ± standard deviation. ** P<0.01, compared with the NC group. shRNA, short hairpin RNA; NC, negative control.
Rabbit Anti Mmp2, supplied by Cusabio, 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/product/rabbit+anti+mmp+2+pab/Rabbit+anti-Human+MMP2+Polyclonal+Antibody/bio_rxiv__2020__09__30__320960-224-18-20
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96
Cell Signaling Technology Inc rabbit polyclonal anti human mmp2 antibody
Primer sequence.
Rabbit Polyclonal Anti Human Mmp2 Antibody, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+mmp+2+pab/MMP-2+Antibody/pmc06304207-59-13-18
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99
Cell Signaling Technology Inc rabbit anti mmp2
Primer sequence.
Rabbit Anti Mmp2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+mmp+2+pab/Phospho-Akt+(Ser473)+XP+Rabbit+mAb/pmc11874121-105-4-8
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96
Cell Signaling Technology Inc anti mmp2
Primer sequence.
Anti Mmp2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+mmp+2+pab/MMP-2+Rabbit+mAb/10__1158_slash_0008___5472__can___21___0431-58-46-59
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95
Cell Signaling Technology Inc anti matrix metalloproteinase 2
Primer sequence.
Anti Matrix Metalloproteinase 2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+mmp+2+pab/MMP-2+Rabbit+mAb/pm36306621-89-12-16
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Image Search Results


Relative mRNA expression rates of genes in chondrocytes by PCR. (A) SELE. (B) MMP2. (C) COL1. * P < 0.05, ** P < 0.01, *** P < 0.001 versus the IL-1β group.

Journal: ACS Omega

Article Title: Mechanisms and Molecular Targets of BuShenHuoXue Formula for Osteoarthritis

doi: 10.1021/acsomega.1c07270

Figure Lengend Snippet: Relative mRNA expression rates of genes in chondrocytes by PCR. (A) SELE. (B) MMP2. (C) COL1. * P < 0.05, ** P < 0.01, *** P < 0.001 versus the IL-1β group.

Article Snippet: The following antibodies and corresponding dilution ratios were used: anti-SELE (bs-1273R, Rabbit, Bioss, 1:500, secondary antibody: 1:5000), anti-MMP2 (bs-0412R, Rabbit, Bioss, 1:500, secondary antibody: 1:5000), anti-CoL1 (bs-10423R, Rabbit, Bioss, 1:500, secondary antibody: 1:5000), and anti-GAPDH (60004-1-lg, Mouse, Proteintech, 120,000, secondary antibody, 1:5000).

Techniques: Expressing

Western blot in five groups of chondrocytes. (A) SELE. (B) MMP2. (C) COL1. (D) Electrophoretic images. ** P < 0.01, *** P < 0.001 versus IL-1β group.

Journal: ACS Omega

Article Title: Mechanisms and Molecular Targets of BuShenHuoXue Formula for Osteoarthritis

doi: 10.1021/acsomega.1c07270

Figure Lengend Snippet: Western blot in five groups of chondrocytes. (A) SELE. (B) MMP2. (C) COL1. (D) Electrophoretic images. ** P < 0.01, *** P < 0.001 versus IL-1β group.

Article Snippet: The following antibodies and corresponding dilution ratios were used: anti-SELE (bs-1273R, Rabbit, Bioss, 1:500, secondary antibody: 1:5000), anti-MMP2 (bs-0412R, Rabbit, Bioss, 1:500, secondary antibody: 1:5000), anti-CoL1 (bs-10423R, Rabbit, Bioss, 1:500, secondary antibody: 1:5000), and anti-GAPDH (60004-1-lg, Mouse, Proteintech, 120,000, secondary antibody, 1:5000).

Techniques: Western Blot

KEGG Enrichment Analysis

Journal: ACS Omega

Article Title: Mechanisms and Molecular Targets of BuShenHuoXue Formula for Osteoarthritis

doi: 10.1021/acsomega.1c07270

Figure Lengend Snippet: KEGG Enrichment Analysis

Article Snippet: The following antibodies and corresponding dilution ratios were used: anti-SELE (bs-1273R, Rabbit, Bioss, 1:500, secondary antibody: 1:5000), anti-MMP2 (bs-0412R, Rabbit, Bioss, 1:500, secondary antibody: 1:5000), anti-CoL1 (bs-10423R, Rabbit, Bioss, 1:500, secondary antibody: 1:5000), and anti-GAPDH (60004-1-lg, Mouse, Proteintech, 120,000, secondary antibody, 1:5000).

Techniques:

PCR Primer Sequences

Journal: ACS Omega

Article Title: Mechanisms and Molecular Targets of BuShenHuoXue Formula for Osteoarthritis

doi: 10.1021/acsomega.1c07270

Figure Lengend Snippet: PCR Primer Sequences

Article Snippet: The following antibodies and corresponding dilution ratios were used: anti-SELE (bs-1273R, Rabbit, Bioss, 1:500, secondary antibody: 1:5000), anti-MMP2 (bs-0412R, Rabbit, Bioss, 1:500, secondary antibody: 1:5000), anti-CoL1 (bs-10423R, Rabbit, Bioss, 1:500, secondary antibody: 1:5000), and anti-GAPDH (60004-1-lg, Mouse, Proteintech, 120,000, secondary antibody, 1:5000).

Techniques: Sequencing

Girdin silencing inhibits the expression and activity of MMP-2 and MMP-9. (A and B) Changes in the mRNA levels of MMP-2 and MMP-9 were measured using reverse transcription-quantitative polymerase chain reaction following transfection. The relative mRNA expression levels were calculated using the 2 −ΔΔCt method. (C and D) Following transfection, changes in the protein levels of MMP-2 and MMP-9 were detected using western blot analysis. (E and F) Following transfection, gelatin zymography was performed to detect changes in the activities of MMP-2 and MMP-9. Each experiment was repeated three times. The experimental results are presented as the mean ± standard deviation. ** P<0.01, compared with the NC group. shRNA, short hairpin RNA; NC, negative control.

Journal: Molecular Medicine Reports

Article Title: Girdin regulates the migration and invasion of glioma cells via the PI3K-Akt signaling pathway

doi: 10.3892/mmr.2015.4049

Figure Lengend Snippet: Girdin silencing inhibits the expression and activity of MMP-2 and MMP-9. (A and B) Changes in the mRNA levels of MMP-2 and MMP-9 were measured using reverse transcription-quantitative polymerase chain reaction following transfection. The relative mRNA expression levels were calculated using the 2 −ΔΔCt method. (C and D) Following transfection, changes in the protein levels of MMP-2 and MMP-9 were detected using western blot analysis. (E and F) Following transfection, gelatin zymography was performed to detect changes in the activities of MMP-2 and MMP-9. Each experiment was repeated three times. The experimental results are presented as the mean ± standard deviation. ** P<0.01, compared with the NC group. shRNA, short hairpin RNA; NC, negative control.

Article Snippet: Following washing with Tris-buffered saline with 0.05% Tween-20 (TBST), the membranes were incubated with the following primary antibodies at 4°C overnight: Rabbit anti-human polyclonal antibody against girdin (1:500 diluted; cat. no. bs-5150R; Bioss, Beijing, China); rabbit anti-human polyclonal antibody against MMP-2 (1:1,000 diluted; cat. no. WL0657); rabbit anti-human polyclonal antibody against MMP-9 (1:1,000 diluted; cat. no. WL0884); rabbit anti-human polyclonal antibody against P85α (1:1,000 diluted; cat. no. WL0191); rabbit anti-human polyclonal antibody against P110α (1:1,000 diluted; cat. no. WL0339); rabbit anti-human polyclonal antibody against AKT (1:1,000 diluted; cat. no. WL0003); rabbit anti-human polyclonal antibody against p-AKT (1:1,000 diluted; cat. no. WLP001).

Techniques: Expressing, Activity Assay, Real-time Polymerase Chain Reaction, Transfection, Western Blot, Zymography, Standard Deviation, shRNA, Negative Control

Primer sequence.

Journal: Stem Cells International

Article Title: Guanylate-Binding Protein 1 Promotes Migration and Invasion of Human Periodontal Ligament Stem Cells

doi: 10.1155/2018/6082956

Figure Lengend Snippet: Primer sequence.

Article Snippet: Antibodies used in this study includes rabbit polyclonal anti-human GBP1 antibody (Invitrogen) and rabbit polyclonal anti-human MMP2 antibody (Cell Signaling Technology).

Techniques: Sequencing

GBP1 is required for upregulation of MMP2 by IFN- γ treatment in PDLSCs. RT-qPCR analysis of matrix metalloproteinase gene expression after 48 hours of IFN- γ treatment in PDLSCs and control cells (a–d). MMP2 expression was upregulated by IFN- γ treatment in a dose-dependent manner (b and e). The IFN- γ -induced upregulation of MMP2 was inhibited by depletion of GBP1 as determined by RT-qPCR analysis and Western blot (f and g). ∗∗ p < 0.01; ∗∗∗ p < 0.001.

Journal: Stem Cells International

Article Title: Guanylate-Binding Protein 1 Promotes Migration and Invasion of Human Periodontal Ligament Stem Cells

doi: 10.1155/2018/6082956

Figure Lengend Snippet: GBP1 is required for upregulation of MMP2 by IFN- γ treatment in PDLSCs. RT-qPCR analysis of matrix metalloproteinase gene expression after 48 hours of IFN- γ treatment in PDLSCs and control cells (a–d). MMP2 expression was upregulated by IFN- γ treatment in a dose-dependent manner (b and e). The IFN- γ -induced upregulation of MMP2 was inhibited by depletion of GBP1 as determined by RT-qPCR analysis and Western blot (f and g). ∗∗ p < 0.01; ∗∗∗ p < 0.001.

Article Snippet: Antibodies used in this study includes rabbit polyclonal anti-human GBP1 antibody (Invitrogen) and rabbit polyclonal anti-human MMP2 antibody (Cell Signaling Technology).

Techniques: Quantitative RT-PCR, Gene Expression, Control, Expressing, Western Blot