prism 5.0 software package 680 Search Results


goat anti mouse 680  (Biotium)
94
Biotium goat anti mouse 680
Goat Anti Mouse 680, supplied by Biotium, 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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hexamethylphosphoramide  (Chem Impex International)
95
Chem Impex International hexamethylphosphoramide
Hexamethylphosphoramide, supplied by Chem Impex International, 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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polystyrene 680  (PS Japan Corporation)
90
PS Japan Corporation polystyrene 680
Polystyrene 680, supplied by PS Japan Corporation, 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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algin high•g series il-6g  (Kimica Corporation)
90
Kimica Corporation algin high•g series il-6g
Algin High•G Series Il 6g, supplied by Kimica Corporation, 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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antichicken  (Jackson Immuno)
94
Jackson Immuno antichicken
Antichicken, supplied by Jackson Immuno, 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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h3k9me1  (Millipore)
90
Millipore h3k9me1
Histone H3K9me2 and H3K27me1 levels in mat4. A, Immunoblot assays with antibodies against <t>H3K9me1,</t> H3K9me2, and H3K27me1 in L119, ddm1, and mat4. H3 was the loading control. B, Statistical analyses of relative signal intensity in A. We set the signal intensity of L119 as 100 to calculate the relative signal intensity of other mutants. Error bars are the means ± sd (n = 3). Asterisks indicate significant differences determined by Student’s t test (*P < 0.05 and ** P < 0.01). C, Histone methylation patterns of H3K9me1 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. D, Histone methylation patterns of H3K9me2 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. E, Histone methylation patterns of H3K27me1 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. For C to E, on the right, the graphs show the percentage of nuclei with condensed or dispersed signal; gray represents a condensed, and white represents a dispersed signal. n = number of nuclei. DAPI stains the pericentromeric heterochromatin regions. F, Detection of H3K9me2 in L119, ddm1, and mat4 at several selected loci by ChIP combined with RT-qPCR. Three independent experiments were conducted with similar results. Data are from one experiment with three technical replicates. Error bars are the means ± sd (n = 3). Asterisks indicate significant differences determined by Student’s t test (*P < 0.05 and **P < 0.01).
H3k9me1, supplied by Millipore, 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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ultra violet uv visible spectrophotometer  (Shimadzu Corporation)
99
Shimadzu Corporation ultra violet uv visible spectrophotometer
Histone H3K9me2 and H3K27me1 levels in mat4. A, Immunoblot assays with antibodies against <t>H3K9me1,</t> H3K9me2, and H3K27me1 in L119, ddm1, and mat4. H3 was the loading control. B, Statistical analyses of relative signal intensity in A. We set the signal intensity of L119 as 100 to calculate the relative signal intensity of other mutants. Error bars are the means ± sd (n = 3). Asterisks indicate significant differences determined by Student’s t test (*P < 0.05 and ** P < 0.01). C, Histone methylation patterns of H3K9me1 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. D, Histone methylation patterns of H3K9me2 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. E, Histone methylation patterns of H3K27me1 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. For C to E, on the right, the graphs show the percentage of nuclei with condensed or dispersed signal; gray represents a condensed, and white represents a dispersed signal. n = number of nuclei. DAPI stains the pericentromeric heterochromatin regions. F, Detection of H3K9me2 in L119, ddm1, and mat4 at several selected loci by ChIP combined with RT-qPCR. Three independent experiments were conducted with similar results. Data are from one experiment with three technical replicates. Error bars are the means ± sd (n = 3). Asterisks indicate significant differences determined by Student’s t test (*P < 0.05 and **P < 0.01).
Ultra Violet Uv Visible Spectrophotometer, supplied by Shimadzu Corporation, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ar antibodies pg21 06–680  (Millipore)
90
Millipore ar antibodies pg21 06–680
Histone H3K9me2 and H3K27me1 levels in mat4. A, Immunoblot assays with antibodies against <t>H3K9me1,</t> H3K9me2, and H3K27me1 in L119, ddm1, and mat4. H3 was the loading control. B, Statistical analyses of relative signal intensity in A. We set the signal intensity of L119 as 100 to calculate the relative signal intensity of other mutants. Error bars are the means ± sd (n = 3). Asterisks indicate significant differences determined by Student’s t test (*P < 0.05 and ** P < 0.01). C, Histone methylation patterns of H3K9me1 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. D, Histone methylation patterns of H3K9me2 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. E, Histone methylation patterns of H3K27me1 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. For C to E, on the right, the graphs show the percentage of nuclei with condensed or dispersed signal; gray represents a condensed, and white represents a dispersed signal. n = number of nuclei. DAPI stains the pericentromeric heterochromatin regions. F, Detection of H3K9me2 in L119, ddm1, and mat4 at several selected loci by ChIP combined with RT-qPCR. Three independent experiments were conducted with similar results. Data are from one experiment with three technical replicates. Error bars are the means ± sd (n = 3). Asterisks indicate significant differences determined by Student’s t test (*P < 0.05 and **P < 0.01).
Ar Antibodies Pg21 06–680, supplied by Millipore, 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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thermoplastic polyurethane elastomer (elastollan 680-50  (Takeda)
90
Takeda thermoplastic polyurethane elastomer (elastollan 680-50
Histone H3K9me2 and H3K27me1 levels in mat4. A, Immunoblot assays with antibodies against <t>H3K9me1,</t> H3K9me2, and H3K27me1 in L119, ddm1, and mat4. H3 was the loading control. B, Statistical analyses of relative signal intensity in A. We set the signal intensity of L119 as 100 to calculate the relative signal intensity of other mutants. Error bars are the means ± sd (n = 3). Asterisks indicate significant differences determined by Student’s t test (*P < 0.05 and ** P < 0.01). C, Histone methylation patterns of H3K9me1 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. D, Histone methylation patterns of H3K9me2 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. E, Histone methylation patterns of H3K27me1 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. For C to E, on the right, the graphs show the percentage of nuclei with condensed or dispersed signal; gray represents a condensed, and white represents a dispersed signal. n = number of nuclei. DAPI stains the pericentromeric heterochromatin regions. F, Detection of H3K9me2 in L119, ddm1, and mat4 at several selected loci by ChIP combined with RT-qPCR. Three independent experiments were conducted with similar results. Data are from one experiment with three technical replicates. Error bars are the means ± sd (n = 3). Asterisks indicate significant differences determined by Student’s t test (*P < 0.05 and **P < 0.01).
Thermoplastic Polyurethane Elastomer (Elastollan 680 50, supplied by Takeda, 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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collimated led light source  (Thorlabs)
90
Thorlabs collimated led light source
Histone H3K9me2 and H3K27me1 levels in mat4. A, Immunoblot assays with antibodies against <t>H3K9me1,</t> H3K9me2, and H3K27me1 in L119, ddm1, and mat4. H3 was the loading control. B, Statistical analyses of relative signal intensity in A. We set the signal intensity of L119 as 100 to calculate the relative signal intensity of other mutants. Error bars are the means ± sd (n = 3). Asterisks indicate significant differences determined by Student’s t test (*P < 0.05 and ** P < 0.01). C, Histone methylation patterns of H3K9me1 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. D, Histone methylation patterns of H3K9me2 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. E, Histone methylation patterns of H3K27me1 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. For C to E, on the right, the graphs show the percentage of nuclei with condensed or dispersed signal; gray represents a condensed, and white represents a dispersed signal. n = number of nuclei. DAPI stains the pericentromeric heterochromatin regions. F, Detection of H3K9me2 in L119, ddm1, and mat4 at several selected loci by ChIP combined with RT-qPCR. Three independent experiments were conducted with similar results. Data are from one experiment with three technical replicates. Error bars are the means ± sd (n = 3). Asterisks indicate significant differences determined by Student’s t test (*P < 0.05 and **P < 0.01).
Collimated Led Light Source, supplied by Thorlabs, 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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aurora a inhibitor vx 680  (Selleck Chemicals)
93
Selleck Chemicals aurora a inhibitor vx 680
Histone H3K9me2 and H3K27me1 levels in mat4. A, Immunoblot assays with antibodies against <t>H3K9me1,</t> H3K9me2, and H3K27me1 in L119, ddm1, and mat4. H3 was the loading control. B, Statistical analyses of relative signal intensity in A. We set the signal intensity of L119 as 100 to calculate the relative signal intensity of other mutants. Error bars are the means ± sd (n = 3). Asterisks indicate significant differences determined by Student’s t test (*P < 0.05 and ** P < 0.01). C, Histone methylation patterns of H3K9me1 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. D, Histone methylation patterns of H3K9me2 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. E, Histone methylation patterns of H3K27me1 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. For C to E, on the right, the graphs show the percentage of nuclei with condensed or dispersed signal; gray represents a condensed, and white represents a dispersed signal. n = number of nuclei. DAPI stains the pericentromeric heterochromatin regions. F, Detection of H3K9me2 in L119, ddm1, and mat4 at several selected loci by ChIP combined with RT-qPCR. Three independent experiments were conducted with similar results. Data are from one experiment with three technical replicates. Error bars are the means ± sd (n = 3). Asterisks indicate significant differences determined by Student’s t test (*P < 0.05 and **P < 0.01).
Aurora A Inhibitor Vx 680, supplied by Selleck Chemicals, 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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mouse il 1β  (Miltenyi Biotec)
94
Miltenyi Biotec mouse il 1β
Histone H3K9me2 and H3K27me1 levels in mat4. A, Immunoblot assays with antibodies against <t>H3K9me1,</t> H3K9me2, and H3K27me1 in L119, ddm1, and mat4. H3 was the loading control. B, Statistical analyses of relative signal intensity in A. We set the signal intensity of L119 as 100 to calculate the relative signal intensity of other mutants. Error bars are the means ± sd (n = 3). Asterisks indicate significant differences determined by Student’s t test (*P < 0.05 and ** P < 0.01). C, Histone methylation patterns of H3K9me1 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. D, Histone methylation patterns of H3K9me2 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. E, Histone methylation patterns of H3K27me1 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. For C to E, on the right, the graphs show the percentage of nuclei with condensed or dispersed signal; gray represents a condensed, and white represents a dispersed signal. n = number of nuclei. DAPI stains the pericentromeric heterochromatin regions. F, Detection of H3K9me2 in L119, ddm1, and mat4 at several selected loci by ChIP combined with RT-qPCR. Three independent experiments were conducted with similar results. Data are from one experiment with three technical replicates. Error bars are the means ± sd (n = 3). Asterisks indicate significant differences determined by Student’s t test (*P < 0.05 and **P < 0.01).
Mouse Il 1β, supplied by Miltenyi Biotec, 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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Image Search Results


Histone H3K9me2 and H3K27me1 levels in mat4. A, Immunoblot assays with antibodies against H3K9me1, H3K9me2, and H3K27me1 in L119, ddm1, and mat4. H3 was the loading control. B, Statistical analyses of relative signal intensity in A. We set the signal intensity of L119 as 100 to calculate the relative signal intensity of other mutants. Error bars are the means ± sd (n = 3). Asterisks indicate significant differences determined by Student’s t test (*P < 0.05 and ** P < 0.01). C, Histone methylation patterns of H3K9me1 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. D, Histone methylation patterns of H3K9me2 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. E, Histone methylation patterns of H3K27me1 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. For C to E, on the right, the graphs show the percentage of nuclei with condensed or dispersed signal; gray represents a condensed, and white represents a dispersed signal. n = number of nuclei. DAPI stains the pericentromeric heterochromatin regions. F, Detection of H3K9me2 in L119, ddm1, and mat4 at several selected loci by ChIP combined with RT-qPCR. Three independent experiments were conducted with similar results. Data are from one experiment with three technical replicates. Error bars are the means ± sd (n = 3). Asterisks indicate significant differences determined by Student’s t test (*P < 0.05 and **P < 0.01).

Journal: Plant Physiology

Article Title: METHIONINE ADENOSYLTRANSFERASE4 Mediates DNA and Histone Methylation 1 [OPEN]

doi: 10.1104/pp.18.00183

Figure Lengend Snippet: Histone H3K9me2 and H3K27me1 levels in mat4. A, Immunoblot assays with antibodies against H3K9me1, H3K9me2, and H3K27me1 in L119, ddm1, and mat4. H3 was the loading control. B, Statistical analyses of relative signal intensity in A. We set the signal intensity of L119 as 100 to calculate the relative signal intensity of other mutants. Error bars are the means ± sd (n = 3). Asterisks indicate significant differences determined by Student’s t test (*P < 0.05 and ** P < 0.01). C, Histone methylation patterns of H3K9me1 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. D, Histone methylation patterns of H3K9me2 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. E, Histone methylation patterns of H3K27me1 in the nuclei of L119, ddm1, and mat4 as detected by immunofluorescence assay. For C to E, on the right, the graphs show the percentage of nuclei with condensed or dispersed signal; gray represents a condensed, and white represents a dispersed signal. n = number of nuclei. DAPI stains the pericentromeric heterochromatin regions. F, Detection of H3K9me2 in L119, ddm1, and mat4 at several selected loci by ChIP combined with RT-qPCR. Three independent experiments were conducted with similar results. Data are from one experiment with three technical replicates. Error bars are the means ± sd (n = 3). Asterisks indicate significant differences determined by Student’s t test (*P < 0.05 and **P < 0.01).

Article Snippet: The primary antibodies used in this assay were H3K9me1 (Millipore; 17-680, 1:50, rabbit), H3K9me2 (Abcam; ab1220, 1:100, mouse), H3K27me1 (Millipore; 07-448, 1:100, rabbit), and H3K4me3 (Millipore; 07-473, 1:100, rabbit).

Techniques: Western Blot, Methylation, Immunofluorescence, Quantitative RT-PCR