Review



valinomycin  (Macklin Inc)

 
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
    • 86
      Buy from Supplier

    Structured Review

    Macklin Inc valinomycin
    Valinomycin, supplied by Macklin Inc, 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/valinomycin/valinomycin/pm41547512-51-2-6
    Average 86 stars, based on 1 article reviews
    valinomycin - by Bioz Stars, 2026-10
    86/100 stars

    Images

    Related Articles

    other:

    Article Title: Byway for fattening: possible role of inhibition of lipolytic enzymes by ionophore.
    Article Snippet: Non-target action of permitted and developing medications is their immanent characteristic which is usually tried to be limited or minimized but is sometimes unsuccessful.. To wit, several widely applied antimicrobials (e. g., monensin, lasalocid) being ionophores have a surprising modulatory effect in metabolic processes some of which cannot be connected to their main activity directly.. To reveal possible off-targets, a sample group of 34 ionophores without or with metal ions was firstly modeled in complexes with 10 different lipolytic fungal enzymes via molecular docking followed by molecular dynamics.

    Blocking Assay:

    Article Title: Human Joint Enabled Flexible Self-Sustainable Sweat Sensors
    Article Snippet: Flexible and wearable electronics have presented a wide range of advantages to non-invasive real-time human health monitoring.. However, its remarkable energy consumption during continuous and long-time operation brings essential, practical challenges, which lead to growing recognition of exploring new and efficient energy strategies for wearables.. Here, inspired by human joints as a biomechanical energy source that shows an ideal option for sustainable powers, we design a battery-free sweat sensing system integrated with sweat resistant selfsustainable energy supply and wireless communication interface, where piezoelectric nanogenerators (PENGs) efficiently converting biomechanical energy from freely movable joints (finger, cubital fossa and popliteal space) into electricity serving as the self-powering module.

    Polymer:

    Article Title: Human Joint Enabled Flexible Self-Sustainable Sweat Sensors
    Article Snippet: Flexible and wearable electronics have presented a wide range of advantages to non-invasive real-time human health monitoring.. However, its remarkable energy consumption during continuous and long-time operation brings essential, practical challenges, which lead to growing recognition of exploring new and efficient energy strategies for wearables.. Here, inspired by human joints as a biomechanical energy source that shows an ideal option for sustainable powers, we design a battery-free sweat sensing system integrated with sweat resistant selfsustainable energy supply and wireless communication interface, where piezoelectric nanogenerators (PENGs) efficiently converting biomechanical energy from freely movable joints (finger, cubital fossa and popliteal space) into electricity serving as the self-powering module.

    High Performance Liquid Chromatography:

    Article Title: Metabolomic insights into the role of isoleucine in regulating Cereulide biosynthesis in emetic Bacillus cereus
    Article Snippet: Bacillus cereus is a significant cause of foodborne illnesses, particularly through starchy foods like rice and pasta, leading to the vomiting symptom.. The primary toxin involved, cereulide, is preformed within contaminated food and exhibits high resistance to heat, making it particularly difficult to control.. Since cereulide persists even after standard food processing methods, its prevention and control remain critical for the food industry.

    Mass Spectrometry:

    Article Title: Metabolomic insights into the role of isoleucine in regulating Cereulide biosynthesis in emetic Bacillus cereus
    Article Snippet: Bacillus cereus is a significant cause of foodborne illnesses, particularly through starchy foods like rice and pasta, leading to the vomiting symptom.. The primary toxin involved, cereulide, is preformed within contaminated food and exhibits high resistance to heat, making it particularly difficult to control.. Since cereulide persists even after standard food processing methods, its prevention and control remain critical for the food industry.



    Similar Products

    valinomycin  (Thermo Fisher)
    94
    Thermo Fisher valinomycin
    Valinomycin, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/valinomycin/Valinomycin%2C+90%2B%25/pmc13156607-123-0-1
    Average 94 stars, based on 1 article reviews
    valinomycin - by Bioz Stars, 2026-10
    94/100 stars
    		  Buy from Supplier
    valinomycin  (Tocris)
    94
    Tocris valinomycin
    Valinomycin, supplied by Tocris, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/valinomycin/Valinomycin/bio_rxiv__64898__2026__04__03__716369-233-29-30
    Average 94 stars, based on 1 article reviews
    valinomycin - by Bioz Stars, 2026-10
    94/100 stars
    		  Buy from Supplier
    valinomycin  (TargetMol)
    94
    TargetMol valinomycin
    Evaluation of MitoQUMA as a fluorescent probe for mtRNA G4s. (A) Fluorescence emission spectra of 1 µ m MitoQUMA with or without 3 µ m of different mtRNAs (mtRNA G4s: Mito152, Mito125, Mito126, Mito155, Mito3; double‐stranded mtRNA: HP18; single‐stranded mtRNA: SS12) and mtDNA G4s (Mito130, Mito27, Mito0.5‐22). (B) Fluorescence emission change of 1 µ m MitoQUMA at 630 nm vs. [mt‐nucleic acids]/[ MitoQUMA ]at λ ex = 555 nm. (C–F) Live HeLa cells were treated with 5 µ m IMT1 (C), 200 µg/mL chloramphenicol (CAPr) (D), varying concentrations of RHPS4 (E), <t>valinomycin</t> (10 µ m together with 200 m m KCl) or ionomycin (20 µ m together with 20 m m KCl) (F), and stained with 2 µ m MitoQUMA . (G) Confocal image of live HeLa cells with overexpression of GFP‐tagged GRSF1 were stained with 2 µ m MitoQUMA . Fluorescence intensity profiles across the yellow line in the white box were shown. (H) Live HeLa cells were transfected with siRNA to knock down GRSF1 expression, followed by staining with 2 µ m MitoQUMA . For each sample of cell image, approximately 100 cells were measured. Biological replicates ( n = 3) were taken. The data are presented as mean ± SEM, and statistical significance is determined by the two‐sided Student's unpaired t‐ test (C, D, G, and H) and one‐way ANOVA followed by Turkey's multiple‐comparison test (E and F) as (ns) not significant, ( * ) p <0.05, ( ** ) p < 0.01, and ( *** ) p < 0.001. Scale bars for cell image: 10 µm.
    Valinomycin, supplied by TargetMol, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/valinomycin/RHPS4/pmc13104114-193-13-14
    Average 94 stars, based on 1 article reviews
    valinomycin - by Bioz Stars, 2026-10
    94/100 stars
    		  Buy from Supplier
    chloramphenicol t1205  (TargetMol)
    94
    TargetMol chloramphenicol t1205
    Evaluation of MitoQUMA as a fluorescent probe for mtRNA G4s. (A) Fluorescence emission spectra of 1 µ m MitoQUMA with or without 3 µ m of different mtRNAs (mtRNA G4s: Mito152, Mito125, Mito126, Mito155, Mito3; double‐stranded mtRNA: HP18; single‐stranded mtRNA: SS12) and mtDNA G4s (Mito130, Mito27, Mito0.5‐22). (B) Fluorescence emission change of 1 µ m MitoQUMA at 630 nm vs. [mt‐nucleic acids]/[ MitoQUMA ]at λ ex = 555 nm. (C–F) Live HeLa cells were treated with 5 µ m IMT1 (C), 200 µg/mL chloramphenicol (CAPr) (D), varying concentrations of RHPS4 (E), <t>valinomycin</t> (10 µ m together with 200 m m KCl) or ionomycin (20 µ m together with 20 m m KCl) (F), and stained with 2 µ m MitoQUMA . (G) Confocal image of live HeLa cells with overexpression of GFP‐tagged GRSF1 were stained with 2 µ m MitoQUMA . Fluorescence intensity profiles across the yellow line in the white box were shown. (H) Live HeLa cells were transfected with siRNA to knock down GRSF1 expression, followed by staining with 2 µ m MitoQUMA . For each sample of cell image, approximately 100 cells were measured. Biological replicates ( n = 3) were taken. The data are presented as mean ± SEM, and statistical significance is determined by the two‐sided Student's unpaired t‐ test (C, D, G, and H) and one‐way ANOVA followed by Turkey's multiple‐comparison test (E and F) as (ns) not significant, ( * ) p <0.05, ( ** ) p < 0.01, and ( *** ) p < 0.001. Scale bars for cell image: 10 µm.
    Chloramphenicol T1205, supplied by TargetMol, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/valinomycin/Valinomycin/pmc13104114-193-15-20
    Average 94 stars, based on 1 article reviews
    chloramphenicol t1205 - by Bioz Stars, 2026-10
    94/100 stars
    		  Buy from Supplier
    valinomycin  (Macklin Inc)
    86
    Macklin Inc valinomycin
    Evaluation of MitoQUMA as a fluorescent probe for mtRNA G4s. (A) Fluorescence emission spectra of 1 µ m MitoQUMA with or without 3 µ m of different mtRNAs (mtRNA G4s: Mito152, Mito125, Mito126, Mito155, Mito3; double‐stranded mtRNA: HP18; single‐stranded mtRNA: SS12) and mtDNA G4s (Mito130, Mito27, Mito0.5‐22). (B) Fluorescence emission change of 1 µ m MitoQUMA at 630 nm vs. [mt‐nucleic acids]/[ MitoQUMA ]at λ ex = 555 nm. (C–F) Live HeLa cells were treated with 5 µ m IMT1 (C), 200 µg/mL chloramphenicol (CAPr) (D), varying concentrations of RHPS4 (E), <t>valinomycin</t> (10 µ m together with 200 m m KCl) or ionomycin (20 µ m together with 20 m m KCl) (F), and stained with 2 µ m MitoQUMA . (G) Confocal image of live HeLa cells with overexpression of GFP‐tagged GRSF1 were stained with 2 µ m MitoQUMA . Fluorescence intensity profiles across the yellow line in the white box were shown. (H) Live HeLa cells were transfected with siRNA to knock down GRSF1 expression, followed by staining with 2 µ m MitoQUMA . For each sample of cell image, approximately 100 cells were measured. Biological replicates ( n = 3) were taken. The data are presented as mean ± SEM, and statistical significance is determined by the two‐sided Student's unpaired t‐ test (C, D, G, and H) and one‐way ANOVA followed by Turkey's multiple‐comparison test (E and F) as (ns) not significant, ( * ) p <0.05, ( ** ) p < 0.01, and ( *** ) p < 0.001. Scale bars for cell image: 10 µm.
    Valinomycin, supplied by Macklin Inc, 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/valinomycin/valinomycin/pm41547512-51-2-6
    Average 86 stars, based on 1 article reviews
    valinomycin - by Bioz Stars, 2026-10
    86/100 stars
    		  Buy from Supplier
    valinomycin  (Merck & Co)
    86
    Merck & Co valinomycin
    Evaluation of MitoQUMA as a fluorescent probe for mtRNA G4s. (A) Fluorescence emission spectra of 1 µ m MitoQUMA with or without 3 µ m of different mtRNAs (mtRNA G4s: Mito152, Mito125, Mito126, Mito155, Mito3; double‐stranded mtRNA: HP18; single‐stranded mtRNA: SS12) and mtDNA G4s (Mito130, Mito27, Mito0.5‐22). (B) Fluorescence emission change of 1 µ m MitoQUMA at 630 nm vs. [mt‐nucleic acids]/[ MitoQUMA ]at λ ex = 555 nm. (C–F) Live HeLa cells were treated with 5 µ m IMT1 (C), 200 µg/mL chloramphenicol (CAPr) (D), varying concentrations of RHPS4 (E), <t>valinomycin</t> (10 µ m together with 200 m m KCl) or ionomycin (20 µ m together with 20 m m KCl) (F), and stained with 2 µ m MitoQUMA . (G) Confocal image of live HeLa cells with overexpression of GFP‐tagged GRSF1 were stained with 2 µ m MitoQUMA . Fluorescence intensity profiles across the yellow line in the white box were shown. (H) Live HeLa cells were transfected with siRNA to knock down GRSF1 expression, followed by staining with 2 µ m MitoQUMA . For each sample of cell image, approximately 100 cells were measured. Biological replicates ( n = 3) were taken. The data are presented as mean ± SEM, and statistical significance is determined by the two‐sided Student's unpaired t‐ test (C, D, G, and H) and one‐way ANOVA followed by Turkey's multiple‐comparison test (E and F) as (ns) not significant, ( * ) p <0.05, ( ** ) p < 0.01, and ( *** ) p < 0.001. Scale bars for cell image: 10 µm.
    Valinomycin, supplied by Merck & Co, 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/valinomycin/valinomycin/pm41498955-39-8-9
    Average 86 stars, based on 1 article reviews
    valinomycin - by Bioz Stars, 2026-10
    86/100 stars
    		  Buy from Supplier

    Image Search Results


    Evaluation of MitoQUMA as a fluorescent probe for mtRNA G4s. (A) Fluorescence emission spectra of 1 µ m MitoQUMA with or without 3 µ m of different mtRNAs (mtRNA G4s: Mito152, Mito125, Mito126, Mito155, Mito3; double‐stranded mtRNA: HP18; single‐stranded mtRNA: SS12) and mtDNA G4s (Mito130, Mito27, Mito0.5‐22). (B) Fluorescence emission change of 1 µ m MitoQUMA at 630 nm vs. [mt‐nucleic acids]/[ MitoQUMA ]at λ ex = 555 nm. (C–F) Live HeLa cells were treated with 5 µ m IMT1 (C), 200 µg/mL chloramphenicol (CAPr) (D), varying concentrations of RHPS4 (E), valinomycin (10 µ m together with 200 m m KCl) or ionomycin (20 µ m together with 20 m m KCl) (F), and stained with 2 µ m MitoQUMA . (G) Confocal image of live HeLa cells with overexpression of GFP‐tagged GRSF1 were stained with 2 µ m MitoQUMA . Fluorescence intensity profiles across the yellow line in the white box were shown. (H) Live HeLa cells were transfected with siRNA to knock down GRSF1 expression, followed by staining with 2 µ m MitoQUMA . For each sample of cell image, approximately 100 cells were measured. Biological replicates ( n = 3) were taken. The data are presented as mean ± SEM, and statistical significance is determined by the two‐sided Student's unpaired t‐ test (C, D, G, and H) and one‐way ANOVA followed by Turkey's multiple‐comparison test (E and F) as (ns) not significant, ( * ) p <0.05, ( ** ) p < 0.01, and ( *** ) p < 0.001. Scale bars for cell image: 10 µm.

    Journal: Advanced Science

    Article Title: Illuminating Mitochondrial RNA G‐Quadruplexes as Structural Brakes on RNA Granule Assembly and OXPHOS

    doi: 10.1002/advs.202523462

    Figure Lengend Snippet: Evaluation of MitoQUMA as a fluorescent probe for mtRNA G4s. (A) Fluorescence emission spectra of 1 µ m MitoQUMA with or without 3 µ m of different mtRNAs (mtRNA G4s: Mito152, Mito125, Mito126, Mito155, Mito3; double‐stranded mtRNA: HP18; single‐stranded mtRNA: SS12) and mtDNA G4s (Mito130, Mito27, Mito0.5‐22). (B) Fluorescence emission change of 1 µ m MitoQUMA at 630 nm vs. [mt‐nucleic acids]/[ MitoQUMA ]at λ ex = 555 nm. (C–F) Live HeLa cells were treated with 5 µ m IMT1 (C), 200 µg/mL chloramphenicol (CAPr) (D), varying concentrations of RHPS4 (E), valinomycin (10 µ m together with 200 m m KCl) or ionomycin (20 µ m together with 20 m m KCl) (F), and stained with 2 µ m MitoQUMA . (G) Confocal image of live HeLa cells with overexpression of GFP‐tagged GRSF1 were stained with 2 µ m MitoQUMA . Fluorescence intensity profiles across the yellow line in the white box were shown. (H) Live HeLa cells were transfected with siRNA to knock down GRSF1 expression, followed by staining with 2 µ m MitoQUMA . For each sample of cell image, approximately 100 cells were measured. Biological replicates ( n = 3) were taken. The data are presented as mean ± SEM, and statistical significance is determined by the two‐sided Student's unpaired t‐ test (C, D, G, and H) and one‐way ANOVA followed by Turkey's multiple‐comparison test (E and F) as (ns) not significant, ( * ) p <0.05, ( ** ) p < 0.01, and ( *** ) p < 0.001. Scale bars for cell image: 10 µm.

    Article Snippet: The treatment concentrations of IMT1 (TargetMol, T8841), Chloramphenicol (TargetMol, T1205), RHPS4 (TargetMol, T6967), Valinomycin (TargetMol, TP1072), Ionomycin (Beyotime, S1672), ICG‐001 (TargetMol, T6113) and BML‐284 (TargetMol, T8820) have been provided in the figure legend.

    Techniques: Fluorescence, Staining, Over Expression, Transfection, Knockdown, Expressing, Comparison