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jam3 sirna  (Sangon Biotech)

 
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    Sangon Biotech jam3 sirna
    Jam3 Sirna, supplied by Sangon Biotech, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/jam3+sirna/pm40711818-94-0-8?v=Sangon+Biotech
    Average 86 stars, based on 1 article reviews
    jam3 sirna - by Bioz Stars, 2026-07
    86/100 stars

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    Figure 1. mRNA and protein expression of Jam3 in HK‑2, Caki‑1 and 786‑0 cells. (A) Western blot analysis was performed to detect the protein level of Jam3, which showed that the protein expression of Jam3 in Caki‑1 and 786‑0 cells was increased compared with that in HK‑2 cells (*P<0.05). (B) Reverse transcription‑polymerase chain reaction analysis was performed to determine the mRNA expression levels of Jam3. Caki‑1 and 786‑0 cells were compared with HK‑2 cells. β‑actin was used as a loading control (*P<0.05). Jam3, junctional adhesion molecule 3; GAPDH, glyceraldehyde 3‑phosphate dehydrogenase.

    Journal: International journal of molecular medicine

    Article Title: Jam3 promotes migration and suppresses apoptosis of renal carcinoma cell lines.

    doi: 10.3892/ijmm.2018.3854

    Figure Lengend Snippet: Figure 1. mRNA and protein expression of Jam3 in HK‑2, Caki‑1 and 786‑0 cells. (A) Western blot analysis was performed to detect the protein level of Jam3, which showed that the protein expression of Jam3 in Caki‑1 and 786‑0 cells was increased compared with that in HK‑2 cells (*P<0.05). (B) Reverse transcription‑polymerase chain reaction analysis was performed to determine the mRNA expression levels of Jam3. Caki‑1 and 786‑0 cells were compared with HK‑2 cells. β‑actin was used as a loading control (*P<0.05). Jam3, junctional adhesion molecule 3; GAPDH, glyceraldehyde 3‑phosphate dehydrogenase.

    Article Snippet: Jam3 small interfering (si)RNA (sc-43872) and negative siRNAs (sc-37007) were obtained from Santa Cruz Biotechnology, Inc.

    Techniques: Expressing, Western Blot, Reverse Transcription Polymerase Chain Reaction, Control

    Figure 2. Increased apoptosis of Caki‑1 and 786‑0 cells transfected with Jam3 siRNA. (A) Cellular Jam3 protein was collected from Caki‑1 and 786‑0 cells transfected with non‑specific siRNA or Jam3 siRNA, and the protein levels of Jam3 in each group were assessed by western blot analysis. GAPDH was used as a loading control (*P<0.05). (B) Effects of Jam3 knockdown on the apoptosis of Caki‑1 and 786‑0 cells were measured using flow cytometry (*P<0.05). Jam3, junctional adhesion molecule 3; GAPDH, glyceraldehyde 3‑phosphate dehydrogenase; siRNA, small interfering RNA; PI, propidium iodide.

    Journal: International journal of molecular medicine

    Article Title: Jam3 promotes migration and suppresses apoptosis of renal carcinoma cell lines.

    doi: 10.3892/ijmm.2018.3854

    Figure Lengend Snippet: Figure 2. Increased apoptosis of Caki‑1 and 786‑0 cells transfected with Jam3 siRNA. (A) Cellular Jam3 protein was collected from Caki‑1 and 786‑0 cells transfected with non‑specific siRNA or Jam3 siRNA, and the protein levels of Jam3 in each group were assessed by western blot analysis. GAPDH was used as a loading control (*P<0.05). (B) Effects of Jam3 knockdown on the apoptosis of Caki‑1 and 786‑0 cells were measured using flow cytometry (*P<0.05). Jam3, junctional adhesion molecule 3; GAPDH, glyceraldehyde 3‑phosphate dehydrogenase; siRNA, small interfering RNA; PI, propidium iodide.

    Article Snippet: Jam3 small interfering (si)RNA (sc-43872) and negative siRNAs (sc-37007) were obtained from Santa Cruz Biotechnology, Inc.

    Techniques: Transfection, Western Blot, Control, Knockdown, Flow Cytometry, Small Interfering RNA

    Figure 3. Jam3 mediates the migration of Caki‑1 and 786‑0 cells. (A) Wound sites/interval between the two wound sites of Caki‑1 cells) were detected and images were captured. Images show the repair of the wound in the two groups (*P<0.05). (B) Wound sites/interval between the two wound sites of 786‑0 cells were measured and images were captured. Images show the repair of the wound in the two groups (*P<0.05). (C) Migration of Caki‑1 and 786‑0 cells was measured using a Transwell chamber (*P<0.05). Original magnification of all images, x200. Jam3, junctional adhesion molecule 3; siRNA, small interfering RNA.

    Journal: International journal of molecular medicine

    Article Title: Jam3 promotes migration and suppresses apoptosis of renal carcinoma cell lines.

    doi: 10.3892/ijmm.2018.3854

    Figure Lengend Snippet: Figure 3. Jam3 mediates the migration of Caki‑1 and 786‑0 cells. (A) Wound sites/interval between the two wound sites of Caki‑1 cells) were detected and images were captured. Images show the repair of the wound in the two groups (*P<0.05). (B) Wound sites/interval between the two wound sites of 786‑0 cells were measured and images were captured. Images show the repair of the wound in the two groups (*P<0.05). (C) Migration of Caki‑1 and 786‑0 cells was measured using a Transwell chamber (*P<0.05). Original magnification of all images, x200. Jam3, junctional adhesion molecule 3; siRNA, small interfering RNA.

    Article Snippet: Jam3 small interfering (si)RNA (sc-43872) and negative siRNAs (sc-37007) were obtained from Santa Cruz Biotechnology, Inc.

    Techniques: Migration, Small Interfering RNA

    Figure 4. Differential expression of E‑cadherin, N‑cadherin, integrin β1 and MMP‑2 in Caki‑1 and 786‑0 cells transfected with non‑specific siRNA and Jam3 siRNA. (A) Cellular protein was collected from Caki‑1 and 786‑0 cells transfected with non‑specific siRNA or Jam3 siRNA. Western blot analysis was performed to assess the levels of E‑cadherin, N‑cadherin, integrin β1, MMP‑2, Bax and Bcl‑2. GAPDH was used as a loading control. (B) Average grey values represented as a histogram (*P<0.05). Jam3, junctional adhesion molecule 3; MMP‑2, matrix metalloproteinase 2; Bcl‑2, B‑cell lymphoma 2; Bax, Bcl‑2‑associated X protein; GAPDH, glyceraldehyde 3‑phosphate dehydrogenase; siRNA, small interfering RNA.

    Journal: International journal of molecular medicine

    Article Title: Jam3 promotes migration and suppresses apoptosis of renal carcinoma cell lines.

    doi: 10.3892/ijmm.2018.3854

    Figure Lengend Snippet: Figure 4. Differential expression of E‑cadherin, N‑cadherin, integrin β1 and MMP‑2 in Caki‑1 and 786‑0 cells transfected with non‑specific siRNA and Jam3 siRNA. (A) Cellular protein was collected from Caki‑1 and 786‑0 cells transfected with non‑specific siRNA or Jam3 siRNA. Western blot analysis was performed to assess the levels of E‑cadherin, N‑cadherin, integrin β1, MMP‑2, Bax and Bcl‑2. GAPDH was used as a loading control. (B) Average grey values represented as a histogram (*P<0.05). Jam3, junctional adhesion molecule 3; MMP‑2, matrix metalloproteinase 2; Bcl‑2, B‑cell lymphoma 2; Bax, Bcl‑2‑associated X protein; GAPDH, glyceraldehyde 3‑phosphate dehydrogenase; siRNA, small interfering RNA.

    Article Snippet: Jam3 small interfering (si)RNA (sc-43872) and negative siRNAs (sc-37007) were obtained from Santa Cruz Biotechnology, Inc.

    Techniques: Quantitative Proteomics, Transfection, Western Blot, Control, Small Interfering RNA