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vectra2 system  (Revvity)


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    Revvity vectra2 system
    Vectra2 System, supplied by Revvity, used in various techniques. Bioz Stars score: 90/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/vectra2+system/Vectra2+Filter+Cube%2C+DAPI%2FQD/pmc10061290-41-28-30
    Average 90 stars, based on 3 article reviews
    vectra2 system - by Bioz Stars, 2026-11
    90/100 stars

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    Related Articles

    Microarray:

    Article Title: Ryanodine receptor 2 promotes colorectal cancer metastasis by the ROS / BACH1 axis
    Article Snippet: .. Tissue microarray (TMA) was constructed from CRC samples embedded in paraffin, and stained with anti‐ RYR2 (diluted 1 : 100), followed by scanning, photographing and scoring using the Vectra2 system (PerkinElmer, Waltham, MA, USA). ..

    Construct:

    Article Title: Ryanodine receptor 2 promotes colorectal cancer metastasis by the ROS / BACH1 axis
    Article Snippet: .. Tissue microarray (TMA) was constructed from CRC samples embedded in paraffin, and stained with anti‐ RYR2 (diluted 1 : 100), followed by scanning, photographing and scoring using the Vectra2 system (PerkinElmer, Waltham, MA, USA). ..

    Staining:

    Article Title: Ryanodine receptor 2 promotes colorectal cancer metastasis by the ROS / BACH1 axis
    Article Snippet: .. Tissue microarray (TMA) was constructed from CRC samples embedded in paraffin, and stained with anti‐ RYR2 (diluted 1 : 100), followed by scanning, photographing and scoring using the Vectra2 system (PerkinElmer, Waltham, MA, USA). ..

    Article Title: Triosephosphate isomerase 1 suppresses growth, migration and invasion of hepatocellular carcinoma cells.
    Article Snippet: Triosephosphate isomerase 1 suppresses growth, migration and invasion of hepatocellular carcinoma cells

    Article Title: CALB1 enhances the interaction between p53 and MDM2, and inhibits the senescence of ovarian cancer cells
    Article Snippet: .. The staining intensity and the protein expression levels were evaluated using the Vectra2 system (PerkinElmer, Inc.). ..

    Expressing:

    Article Title: Triosephosphate isomerase 1 suppresses growth, migration and invasion of hepatocellular carcinoma cells.
    Article Snippet: Triosephosphate isomerase 1 suppresses growth, migration and invasion of hepatocellular carcinoma cells

    Article Title: CALB1 enhances the interaction between p53 and MDM2, and inhibits the senescence of ovarian cancer cells
    Article Snippet: .. The staining intensity and the protein expression levels were evaluated using the Vectra2 system (PerkinElmer, Inc.). ..



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    The Expression of EPB41L4A-AS1 Increases in Placental Tissue of Early RM (A) Real-time PCR was used to determine the levels of significant differences in long non-coding RNAs in early RM placental trophoblast cells after lncRNA microarray (N = 3). EPB41L4A-AS1 was significantly higher in early RM groups (p < 0.05). (B) EPB41L4A-AS1 transcription levels were increased significantly in some pregnancy pathologies (N = 232) (p < 0.01) compared with normal placental tissue: early RM (N = 62, p < 0.01), IUGR (N = 36, p < 0.05), and PE (N = 144, p < 0.05). These data were collected from the GEO database. (C) The expression level of EPB41L4A-AS1 in our clinical sample was statistically higher in early RM placental tissue (N = 45) compared with the controls (N = 23), as shown by real-time PCR. (D) TIGA1 protein expression was increased dramatically in early RM placental tissue, as shown by western blot examination and quantitative analysis (N = 8) by ImageJ software. (E) Immunohistochemical staining of TIGA1 in early RM placental tissue. Quantitative analysis of TIGA1 intensity (N = 40) was performed using PerkinElmer Vectra 2. Stained TIGA1 was significant higher in the early RM group. Data are represented as means ± SD; *p < 0.05, **p < 0.01, Student’s t test.
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    The Expression of EPB41L4A-AS1 Increases in Placental Tissue of Early RM (A) Real-time PCR was used to determine the levels of significant differences in long non-coding RNAs in early RM placental trophoblast cells after lncRNA microarray (N = 3). EPB41L4A-AS1 was significantly higher in early RM groups (p < 0.05). (B) EPB41L4A-AS1 transcription levels were increased significantly in some pregnancy pathologies (N = 232) (p < 0.01) compared with normal placental tissue: early RM (N = 62, p < 0.01), IUGR (N = 36, p < 0.05), and PE (N = 144, p < 0.05). These data were collected from the GEO database. (C) The expression level of EPB41L4A-AS1 in our clinical sample was statistically higher in early RM placental tissue (N = 45) compared with the controls (N = 23), as shown by real-time PCR. (D) TIGA1 protein expression was increased dramatically in early RM placental tissue, as shown by western blot examination and quantitative analysis (N = 8) by ImageJ software. (E) Immunohistochemical staining of TIGA1 in early RM placental tissue. Quantitative analysis of TIGA1 intensity (N = 40) was performed using PerkinElmer Vectra 2. Stained TIGA1 was significant higher in the early RM group. Data are represented as means ± SD; *p < 0.05, **p < 0.01, Student’s t test.
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    Image Search Results


    The Expression of EPB41L4A-AS1 Increases in Placental Tissue of Early RM (A) Real-time PCR was used to determine the levels of significant differences in long non-coding RNAs in early RM placental trophoblast cells after lncRNA microarray (N = 3). EPB41L4A-AS1 was significantly higher in early RM groups (p < 0.05). (B) EPB41L4A-AS1 transcription levels were increased significantly in some pregnancy pathologies (N = 232) (p < 0.01) compared with normal placental tissue: early RM (N = 62, p < 0.01), IUGR (N = 36, p < 0.05), and PE (N = 144, p < 0.05). These data were collected from the GEO database. (C) The expression level of EPB41L4A-AS1 in our clinical sample was statistically higher in early RM placental tissue (N = 45) compared with the controls (N = 23), as shown by real-time PCR. (D) TIGA1 protein expression was increased dramatically in early RM placental tissue, as shown by western blot examination and quantitative analysis (N = 8) by ImageJ software. (E) Immunohistochemical staining of TIGA1 in early RM placental tissue. Quantitative analysis of TIGA1 intensity (N = 40) was performed using PerkinElmer Vectra 2. Stained TIGA1 was significant higher in the early RM group. Data are represented as means ± SD; *p < 0.05, **p < 0.01, Student’s t test.

    Journal: Molecular Therapy. Nucleic Acids

    Article Title: Overexpression of lncRNA EPB41L4A-AS1 Induces Metabolic Reprogramming in Trophoblast Cells and Placenta Tissue of Miscarriage

    doi: 10.1016/j.omtn.2019.09.017

    Figure Lengend Snippet: The Expression of EPB41L4A-AS1 Increases in Placental Tissue of Early RM (A) Real-time PCR was used to determine the levels of significant differences in long non-coding RNAs in early RM placental trophoblast cells after lncRNA microarray (N = 3). EPB41L4A-AS1 was significantly higher in early RM groups (p < 0.05). (B) EPB41L4A-AS1 transcription levels were increased significantly in some pregnancy pathologies (N = 232) (p < 0.01) compared with normal placental tissue: early RM (N = 62, p < 0.01), IUGR (N = 36, p < 0.05), and PE (N = 144, p < 0.05). These data were collected from the GEO database. (C) The expression level of EPB41L4A-AS1 in our clinical sample was statistically higher in early RM placental tissue (N = 45) compared with the controls (N = 23), as shown by real-time PCR. (D) TIGA1 protein expression was increased dramatically in early RM placental tissue, as shown by western blot examination and quantitative analysis (N = 8) by ImageJ software. (E) Immunohistochemical staining of TIGA1 in early RM placental tissue. Quantitative analysis of TIGA1 intensity (N = 40) was performed using PerkinElmer Vectra 2. Stained TIGA1 was significant higher in the early RM group. Data are represented as means ± SD; *p < 0.05, **p < 0.01, Student’s t test.

    Article Snippet: Quantitative analysis of TIGA1 intensity (N = 40) was performed using PerkinElmer Vectra 2.

    Techniques: Expressing, Real-time Polymerase Chain Reaction, Microarray, Western Blot, Software, Immunohistochemical staining, Staining