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hl1 cells  (ApexBio)

 
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    ApexBio hl1 cells
    Hl1 Cells, supplied by ApexBio, 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/hl1+cells/hl1+cells/pm39366645-117-1-9
    Average 90 stars, based on 1 article reviews
    hl1 cells - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    other:

    Article Title: Persistent hypertension induces atrial remodeling and atrial fibrillation through DNA damage and ATM/CHK2/p53 signaling pathway.
    Article Snippet: Atrial fibrillation (AF) is the most prevalent arrhythmia in clinical practice, with hypertension emerging as an independent risk factor.. Previous literature has established associations between DNA damage response (DDR) and autophagy in relation to the pathogenesis of AF.. The aim of this study was to evaluate the effect of atrial DNA damage response in persistent hypertension-induced atrial electrical and structural remodeling, and to further explore the potential therapeutic targets.



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    Effect of PINCH1 on the function of <t>HL1</t> cells. (A) Successful PINCH1 shRNA was confirmed by western blot analysis. (B) Percentage of GFP + cells in PINCH1 shRNA/PINCH1 OE cells following transfection. Untreated cells were used as a negative control. (C) The expression levels of PINCH1 mRNA in control, PINCH1 shRNA, and PINCH1 shRNA/PINCH1 OE cells were determined by qPCR. (D) HL1 cell viability (magnification, x100) and (E) migration ability were decreased following PINCH1 shRNA (magnification, x100). (F) HL1 cell apoptosis rate was significantly increased following PINCH1 shRNA. ** P<0.05 vs. shRNA NC; ## P<0.05 vs. PINCH1 SHRNA/PINCH1 OE group. PINCH1, particularly interesting new cysteine histidine rich 1; PINCH1 shRNA, PINCH1 knockdown; PINCH1 OE, PINCH1 overexpression; PINCH1 SHRNA/PINCH1 OE, PINCH1 overexpression (PINCH1 OE) in PINCH1 shRNA HL1 cells.
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    Effect of PINCH1 on the function of HL1 cells. (A) Successful PINCH1 shRNA was confirmed by western blot analysis. (B) Percentage of GFP + cells in PINCH1 shRNA/PINCH1 OE cells following transfection. Untreated cells were used as a negative control. (C) The expression levels of PINCH1 mRNA in control, PINCH1 shRNA, and PINCH1 shRNA/PINCH1 OE cells were determined by qPCR. (D) HL1 cell viability (magnification, x100) and (E) migration ability were decreased following PINCH1 shRNA (magnification, x100). (F) HL1 cell apoptosis rate was significantly increased following PINCH1 shRNA. ** P<0.05 vs. shRNA NC; ## P<0.05 vs. PINCH1 SHRNA/PINCH1 OE group. PINCH1, particularly interesting new cysteine histidine rich 1; PINCH1 shRNA, PINCH1 knockdown; PINCH1 OE, PINCH1 overexpression; PINCH1 SHRNA/PINCH1 OE, PINCH1 overexpression (PINCH1 OE) in PINCH1 shRNA HL1 cells.

    Journal: Experimental and Therapeutic Medicine

    Article Title: PINCH1 knockout aggravates myocardial infarction in mice via mediating the NF-κB signaling pathway

    doi: 10.3892/etm.2021.10984

    Figure Lengend Snippet: Effect of PINCH1 on the function of HL1 cells. (A) Successful PINCH1 shRNA was confirmed by western blot analysis. (B) Percentage of GFP + cells in PINCH1 shRNA/PINCH1 OE cells following transfection. Untreated cells were used as a negative control. (C) The expression levels of PINCH1 mRNA in control, PINCH1 shRNA, and PINCH1 shRNA/PINCH1 OE cells were determined by qPCR. (D) HL1 cell viability (magnification, x100) and (E) migration ability were decreased following PINCH1 shRNA (magnification, x100). (F) HL1 cell apoptosis rate was significantly increased following PINCH1 shRNA. ** P<0.05 vs. shRNA NC; ## P<0.05 vs. PINCH1 SHRNA/PINCH1 OE group. PINCH1, particularly interesting new cysteine histidine rich 1; PINCH1 shRNA, PINCH1 knockdown; PINCH1 OE, PINCH1 overexpression; PINCH1 SHRNA/PINCH1 OE, PINCH1 overexpression (PINCH1 OE) in PINCH1 shRNA HL1 cells.

    Article Snippet: To determine HL1 cell viability, a Cell Counting Kit 8 (CCK-8) assay was used according to the manufacturer's instructions (Beyotime Institute of Biotechnology).

    Techniques: shRNA, Western Blot, Transfection, Negative Control, Expressing, Control, Migration, Knockdown, Over Expression

    HL1 cell apoptosis is associated with the NF-κB signaling pathway. Expression levels of NF-κB signaling pathway-related proteins were (A) determined by western blotting and (B) semi-quantified. NF-κB, MYD88, TNF-α and caspase-3 expression levels were significantly increased, whereas MMP-2 and MMP-9 expression levels were notably decreased in the shRNA PINCH1 group. ** P<0.01 vs. shRNA NC group. MYD88, myeloid differentiation factor 88; PINCH1, particularly interesting new cysteine histidine rich 1; WT, wild-type; shRNA, short hairpin RNA.

    Journal: Experimental and Therapeutic Medicine

    Article Title: PINCH1 knockout aggravates myocardial infarction in mice via mediating the NF-κB signaling pathway

    doi: 10.3892/etm.2021.10984

    Figure Lengend Snippet: HL1 cell apoptosis is associated with the NF-κB signaling pathway. Expression levels of NF-κB signaling pathway-related proteins were (A) determined by western blotting and (B) semi-quantified. NF-κB, MYD88, TNF-α and caspase-3 expression levels were significantly increased, whereas MMP-2 and MMP-9 expression levels were notably decreased in the shRNA PINCH1 group. ** P<0.01 vs. shRNA NC group. MYD88, myeloid differentiation factor 88; PINCH1, particularly interesting new cysteine histidine rich 1; WT, wild-type; shRNA, short hairpin RNA.

    Article Snippet: To determine HL1 cell viability, a Cell Counting Kit 8 (CCK-8) assay was used according to the manufacturer's instructions (Beyotime Institute of Biotechnology).

    Techniques: Expressing, Western Blot, shRNA