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gs 6.6 software package  (Partek)

 
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    Partek gs 6.6 software package
    miR‐382‐5p overexpression in CB CD 34+ cells. (A) Expression of miR‐382‐5p in CB CD 34+ cells was assessed by means of qRT ‐ PCR at 24 and 48 h after the last nucleofection and data are reported as RQ . U6 sn RNA was used as internal controls, and mimic‐Neg was used as reference sample. The results are representative of six independent experiments and are expressed as the mean ± SEM . Two‐tailed Student's t ‐test: ** P < .01 versus mimic‐Neg. (B) <t>GEP</t> of biological triplicates of miR‐382‐5p‐overexpressing cells and mimic‐Neg control samples. The heatmap was computed on a gene list selected by anova using the clustering algorithm included in <t>the</t> <t>Partek</t> GS package (Partek Incorporated, St Louis, MO , USA ) by means of Euclidean distance and average linkage. Gene coloring is based on normalized signals, as shown at the bottom of the figure; green indicates reduced expression; red increased expression. Gene symbol is indicated on the right. Mir‐382 and mimic‐Neg groups clustered separately in the dendrogram shown at the top of the heat map.
    Gs 6.6 Software Package, supplied by Partek, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/gs+6%2E6+software/pmc06275274-69-0-8?v=Partek
    Average 90 stars, based on 1 article reviews
    gs 6.6 software package - by Bioz Stars, 2026-07
    90/100 stars

    Images

    1) Product Images from "Role of TGF ‐β1/miR‐382‐5p/ SOD 2 axis in the induction of oxidative stress in CD 34+ cells from primary myelofibrosis"

    Article Title: Role of TGF ‐β1/miR‐382‐5p/ SOD 2 axis in the induction of oxidative stress in CD 34+ cells from primary myelofibrosis

    Journal: Molecular Oncology

    doi: 10.1002/1878-0261.12387

    miR‐382‐5p overexpression in CB CD 34+ cells. (A) Expression of miR‐382‐5p in CB CD 34+ cells was assessed by means of qRT ‐ PCR at 24 and 48 h after the last nucleofection and data are reported as RQ . U6 sn RNA was used as internal controls, and mimic‐Neg was used as reference sample. The results are representative of six independent experiments and are expressed as the mean ± SEM . Two‐tailed Student's t ‐test: ** P < .01 versus mimic‐Neg. (B) GEP of biological triplicates of miR‐382‐5p‐overexpressing cells and mimic‐Neg control samples. The heatmap was computed on a gene list selected by anova using the clustering algorithm included in the Partek GS package (Partek Incorporated, St Louis, MO , USA ) by means of Euclidean distance and average linkage. Gene coloring is based on normalized signals, as shown at the bottom of the figure; green indicates reduced expression; red increased expression. Gene symbol is indicated on the right. Mir‐382 and mimic‐Neg groups clustered separately in the dendrogram shown at the top of the heat map.
    Figure Legend Snippet: miR‐382‐5p overexpression in CB CD 34+ cells. (A) Expression of miR‐382‐5p in CB CD 34+ cells was assessed by means of qRT ‐ PCR at 24 and 48 h after the last nucleofection and data are reported as RQ . U6 sn RNA was used as internal controls, and mimic‐Neg was used as reference sample. The results are representative of six independent experiments and are expressed as the mean ± SEM . Two‐tailed Student's t ‐test: ** P < .01 versus mimic‐Neg. (B) GEP of biological triplicates of miR‐382‐5p‐overexpressing cells and mimic‐Neg control samples. The heatmap was computed on a gene list selected by anova using the clustering algorithm included in the Partek GS package (Partek Incorporated, St Louis, MO , USA ) by means of Euclidean distance and average linkage. Gene coloring is based on normalized signals, as shown at the bottom of the figure; green indicates reduced expression; red increased expression. Gene symbol is indicated on the right. Mir‐382 and mimic‐Neg groups clustered separately in the dendrogram shown at the top of the heat map.

    Techniques Used: Over Expression, Expressing, Quantitative RT-PCR, Two Tailed Test, Control



    Similar Products

    gs 6.6 software package  (Partek)
    90
    Partek gs 6.6 software package
    miR‐382‐5p overexpression in CB CD 34+ cells. (A) Expression of miR‐382‐5p in CB CD 34+ cells was assessed by means of qRT ‐ PCR at 24 and 48 h after the last nucleofection and data are reported as RQ . U6 sn RNA was used as internal controls, and mimic‐Neg was used as reference sample. The results are representative of six independent experiments and are expressed as the mean ± SEM . Two‐tailed Student's t ‐test: ** P < .01 versus mimic‐Neg. (B) <t>GEP</t> of biological triplicates of miR‐382‐5p‐overexpressing cells and mimic‐Neg control samples. The heatmap was computed on a gene list selected by anova using the clustering algorithm included in <t>the</t> <t>Partek</t> GS package (Partek Incorporated, St Louis, MO , USA ) by means of Euclidean distance and average linkage. Gene coloring is based on normalized signals, as shown at the bottom of the figure; green indicates reduced expression; red increased expression. Gene symbol is indicated on the right. Mir‐382 and mimic‐Neg groups clustered separately in the dendrogram shown at the top of the heat map.
    Gs 6.6 Software Package, supplied by Partek, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/gs+6%2E6+software/pmc06275274-69-0-8?v=Partek
    Average 90 stars, based on 1 article reviews
    gs 6.6 software package - by Bioz Stars, 2026-07
    90/100 stars
    		  Buy from Supplier
    gs 6.6 software  (Partek)
    90
    Partek gs 6.6 software
    miR‐382‐5p overexpression in CB CD 34+ cells. (A) Expression of miR‐382‐5p in CB CD 34+ cells was assessed by means of qRT ‐ PCR at 24 and 48 h after the last nucleofection and data are reported as RQ . U6 sn RNA was used as internal controls, and mimic‐Neg was used as reference sample. The results are representative of six independent experiments and are expressed as the mean ± SEM . Two‐tailed Student's t ‐test: ** P < .01 versus mimic‐Neg. (B) <t>GEP</t> of biological triplicates of miR‐382‐5p‐overexpressing cells and mimic‐Neg control samples. The heatmap was computed on a gene list selected by anova using the clustering algorithm included in <t>the</t> <t>Partek</t> GS package (Partek Incorporated, St Louis, MO , USA ) by means of Euclidean distance and average linkage. Gene coloring is based on normalized signals, as shown at the bottom of the figure; green indicates reduced expression; red increased expression. Gene symbol is indicated on the right. Mir‐382 and mimic‐Neg groups clustered separately in the dendrogram shown at the top of the heat map.
    Gs 6.6 Software, supplied by Partek, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/gs+6%2E6+software/pmc04715677-98-6-5?v=Partek
    Average 90 stars, based on 1 article reviews
    gs 6.6 software - by Bioz Stars, 2026-07
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    miR‐382‐5p overexpression in CB CD 34+ cells. (A) Expression of miR‐382‐5p in CB CD 34+ cells was assessed by means of qRT ‐ PCR at 24 and 48 h after the last nucleofection and data are reported as RQ . U6 sn RNA was used as internal controls, and mimic‐Neg was used as reference sample. The results are representative of six independent experiments and are expressed as the mean ± SEM . Two‐tailed Student's t ‐test: ** P < .01 versus mimic‐Neg. (B) GEP of biological triplicates of miR‐382‐5p‐overexpressing cells and mimic‐Neg control samples. The heatmap was computed on a gene list selected by anova using the clustering algorithm included in the Partek GS package (Partek Incorporated, St Louis, MO , USA ) by means of Euclidean distance and average linkage. Gene coloring is based on normalized signals, as shown at the bottom of the figure; green indicates reduced expression; red increased expression. Gene symbol is indicated on the right. Mir‐382 and mimic‐Neg groups clustered separately in the dendrogram shown at the top of the heat map.

    Journal: Molecular Oncology

    Article Title: Role of TGF ‐β1/miR‐382‐5p/ SOD 2 axis in the induction of oxidative stress in CD 34+ cells from primary myelofibrosis

    doi: 10.1002/1878-0261.12387

    Figure Lengend Snippet: miR‐382‐5p overexpression in CB CD 34+ cells. (A) Expression of miR‐382‐5p in CB CD 34+ cells was assessed by means of qRT ‐ PCR at 24 and 48 h after the last nucleofection and data are reported as RQ . U6 sn RNA was used as internal controls, and mimic‐Neg was used as reference sample. The results are representative of six independent experiments and are expressed as the mean ± SEM . Two‐tailed Student's t ‐test: ** P < .01 versus mimic‐Neg. (B) GEP of biological triplicates of miR‐382‐5p‐overexpressing cells and mimic‐Neg control samples. The heatmap was computed on a gene list selected by anova using the clustering algorithm included in the Partek GS package (Partek Incorporated, St Louis, MO , USA ) by means of Euclidean distance and average linkage. Gene coloring is based on normalized signals, as shown at the bottom of the figure; green indicates reduced expression; red increased expression. Gene symbol is indicated on the right. Mir‐382 and mimic‐Neg groups clustered separately in the dendrogram shown at the top of the heat map.

    Article Snippet: Gene expression profile (GEP) data were analyzed by partek gs 6.6 Software Package and normalized using the robust multi‐array average (RMA) procedure (Irizarry et al ., ).

    Techniques: Over Expression, Expressing, Quantitative RT-PCR, Two Tailed Test, Control