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ca  (Worthington Biochemical)


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    Structured Review

    Worthington Biochemical ca
    Ca, supplied by Worthington Biochemical, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cas/ca/custom%40ca%4042547993
    Average 99 stars, based on 1 article reviews
    ca - by Bioz Stars, 2026-10
    99/100 stars

    Images

    Related Articles

    Flow Cytometry:

    Article Title: Chamber-specific regulation of myofilament Ca 2+ sensitivity by nNOSβ via troponin I phosphorylation: Predominance in the right ventricle
    Article Snippet: a constant flow rate (8–10 ml·min −1 ) according to the following sequence: (1) 8 min with Ca 2+ -free Tyrode solution; (2) 8 min with Ca 2+ -free Tyrode solution containing collagenase (1 mg·ml −1 ; Worthington Biochemical Co.), protease (0.133 mg·ml −1 ), BSA (1.65 mg·ml −1 ), and Ca 2+ (0.05 mM); and (3) an additional 10 min digestion with collagenase-containing Tyrode solution. The interventri

    Analysis:

    Article Title: Chamber-specific regulation of myofilament Ca 2+ sensitivity by nNOSβ via troponin I phosphorylation: Predominance in the right ventricle
    Article Snippet: a constant flow rate (8–10 ml·min −1 ) according to the following sequence: (1) 8 min with Ca 2+ -free Tyrode solution; (2) 8 min with Ca 2+ -free Tyrode solution containing collagenase (1 mg·ml −1 ; Worthington Biochemical Co.), protease (0.133 mg·ml −1 ), BSA (1.65 mg·ml −1 ), and Ca 2+ (0.05 mM); and (3) an additional 10 min digestion with collagenase-containing Tyrode solution. The interventri

    Glass:

    Article Title: Chamber-specific regulation of myofilament Ca 2+ sensitivity by nNOSβ via troponin I phosphorylation: Predominance in the right ventricle
    Article Snippet: a constant flow rate (8–10 ml·min −1 ) according to the following sequence: (1) 8 min with Ca 2+ -free Tyrode solution; (2) 8 min with Ca 2+ -free Tyrode solution containing collagenase (1 mg·ml −1 ; Worthington Biochemical Co.), protease (0.133 mg·ml −1 ), BSA (1.65 mg·ml −1 ), and Ca 2+ (0.05 mM); and (3) an additional 10 min digestion with collagenase-containing Tyrode solution. The interventri

    Imaging:

    Article Title: Chamber-specific regulation of myofilament Ca 2+ sensitivity by nNOSβ via troponin I phosphorylation: Predominance in the right ventricle
    Article Snippet: a constant flow rate (8–10 ml·min −1 ) according to the following sequence: (1) 8 min with Ca 2+ -free Tyrode solution; (2) 8 min with Ca 2+ -free Tyrode solution containing collagenase (1 mg·ml −1 ; Worthington Biochemical Co.), protease (0.133 mg·ml −1 ), BSA (1.65 mg·ml −1 ), and Ca 2+ (0.05 mM); and (3) an additional 10 min digestion with collagenase-containing Tyrode solution. The interventri

    FISH:

    Article Title: Chamber-specific regulation of myofilament Ca 2+ sensitivity by nNOSβ via troponin I phosphorylation: Predominance in the right ventricle
    Article Snippet: a constant flow rate (8–10 ml·min −1 ) according to the following sequence: (1) 8 min with Ca 2+ -free Tyrode solution; (2) 8 min with Ca 2+ -free Tyrode solution containing collagenase (1 mg·ml −1 ; Worthington Biochemical Co.), protease (0.133 mg·ml −1 ), BSA (1.65 mg·ml −1 ), and Ca 2+ (0.05 mM); and (3) an additional 10 min digestion with collagenase-containing Tyrode solution. The interventri

    Isolation:

    Article Title: Chamber-specific regulation of myofilament Ca 2+ sensitivity by nNOSβ via troponin I phosphorylation: Predominance in the right ventricle
    Article Snippet: a constant flow rate (8–10 ml·min −1 ) according to the following sequence: (1) 8 min with Ca 2+ -free Tyrode solution; (2) 8 min with Ca 2+ -free Tyrode solution containing collagenase (1 mg·ml −1 ; Worthington Biochemical Co.), protease (0.133 mg·ml −1 ), BSA (1.65 mg·ml −1 ), and Ca 2+ (0.05 mM); and (3) an additional 10 min digestion with collagenase-containing Tyrode solution. The interventri

    Oligomer Restriction:

    Article Title: Chamber-specific regulation of myofilament Ca 2+ sensitivity by nNOSβ via troponin I phosphorylation: Predominance in the right ventricle
    Article Snippet: a constant flow rate (8–10 ml·min −1 ) according to the following sequence: (1) 8 min with Ca 2+ -free Tyrode solution; (2) 8 min with Ca 2+ -free Tyrode solution containing collagenase (1 mg·ml −1 ; Worthington Biochemical Co.), protease (0.133 mg·ml −1 ), BSA (1.65 mg·ml −1 ), and Ca 2+ (0.05 mM); and (3) an additional 10 min digestion with collagenase-containing Tyrode solution. The interventri

    Cytometry:

    Article Title: Chamber-specific regulation of myofilament Ca 2+ sensitivity by nNOSβ via troponin I phosphorylation: Predominance in the right ventricle
    Article Snippet: a constant flow rate (8–10 ml·min −1 ) according to the following sequence: (1) 8 min with Ca 2+ -free Tyrode solution; (2) 8 min with Ca 2+ -free Tyrode solution containing collagenase (1 mg·ml −1 ; Worthington Biochemical Co.), protease (0.133 mg·ml −1 ), BSA (1.65 mg·ml −1 ), and Ca 2+ (0.05 mM); and (3) an additional 10 min digestion with collagenase-containing Tyrode solution. The interventri

    Suspension:

    Article Title: Chamber-specific regulation of myofilament Ca 2+ sensitivity by nNOSβ via troponin I phosphorylation: Predominance in the right ventricle
    Article Snippet: a constant flow rate (8–10 ml·min −1 ) according to the following sequence: (1) 8 min with Ca 2+ -free Tyrode solution; (2) 8 min with Ca 2+ -free Tyrode solution containing collagenase (1 mg·ml −1 ; Worthington Biochemical Co.), protease (0.133 mg·ml −1 ), BSA (1.65 mg·ml −1 ), and Ca 2+ (0.05 mM); and (3) an additional 10 min digestion with collagenase-containing Tyrode solution. The interventri

    Expressing:

    Article Title: Chamber-specific regulation of myofilament Ca 2+ sensitivity by nNOSβ via troponin I phosphorylation: Predominance in the right ventricle
    Article Snippet: a constant flow rate (8–10 ml·min −1 ) according to the following sequence: (1) 8 min with Ca 2+ -free Tyrode solution; (2) 8 min with Ca 2+ -free Tyrode solution containing collagenase (1 mg·ml −1 ; Worthington Biochemical Co.), protease (0.133 mg·ml −1 ), BSA (1.65 mg·ml −1 ), and Ca 2+ (0.05 mM); and (3) an additional 10 min digestion with collagenase-containing Tyrode solution. The interventri

    Saline:

    Article Title: Chamber-specific regulation of myofilament Ca 2+ sensitivity by nNOSβ via troponin I phosphorylation: Predominance in the right ventricle
    Article Snippet: a constant flow rate (8–10 ml·min −1 ) according to the following sequence: (1) 8 min with Ca 2+ -free Tyrode solution; (2) 8 min with Ca 2+ -free Tyrode solution containing collagenase (1 mg·ml −1 ; Worthington Biochemical Co.), protease (0.133 mg·ml −1 ), BSA (1.65 mg·ml −1 ), and Ca 2+ (0.05 mM); and (3) an additional 10 min digestion with collagenase-containing Tyrode solution. The interventri

    Plasmid Preparation:

    Article Title: Chamber-specific regulation of myofilament Ca 2+ sensitivity by nNOSβ via troponin I phosphorylation: Predominance in the right ventricle
    Article Snippet: a constant flow rate (8–10 ml·min −1 ) according to the following sequence: (1) 8 min with Ca 2+ -free Tyrode solution; (2) 8 min with Ca 2+ -free Tyrode solution containing collagenase (1 mg·ml −1 ; Worthington Biochemical Co.), protease (0.133 mg·ml −1 ), BSA (1.65 mg·ml −1 ), and Ca 2+ (0.05 mM); and (3) an additional 10 min digestion with collagenase-containing Tyrode solution. The interventri

    Mouse Assay:

    Article Title: Chamber-specific regulation of myofilament Ca 2+ sensitivity by nNOSβ via troponin I phosphorylation: Predominance in the right ventricle
    Article Snippet: a constant flow rate (8–10 ml·min −1 ) according to the following sequence: (1) 8 min with Ca 2+ -free Tyrode solution; (2) 8 min with Ca 2+ -free Tyrode solution containing collagenase (1 mg·ml −1 ; Worthington Biochemical Co.), protease (0.133 mg·ml −1 ), BSA (1.65 mg·ml −1 ), and Ca 2+ (0.05 mM); and (3) an additional 10 min digestion with collagenase-containing Tyrode solution. The interventri



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    ( A ) Schematics of the four possible degradation pathways that CaMKIV-phosphorylated REST can undertake and the three inhibitors that were used to dissect the fate of REST. Cat, cathepsin. ( B ) HEK293T cells were transfected with WT, CA, or KD CaMKIV and treated with cycloheximide (CHX) to in4hibit further translation. Then, cells were treated for 16 hours with either vehicle [dimethyl sulfoxide (DMSO)] or MG-132 (5 μM), an inhibitor of the ubiquitin-proteasome system (UPS). Left: Representative immunoblots monitoring the expression of WT, CA, and KD CaMKs, REST, and calnexin, respectively, in HEK293T cells, 48 hours after transfection with the kinase constructs. Right: Mean (±SEM) REST protein levels, shown as ratios with calnexin immunoreactivity under the various experimental conditions. No effects of inhibition of the UPS were observed. * P = 0.017, CA versus WT in DMSO; ** P = 0.0048, CA versus WT in MG-132. Two-way ANOVA/Tukey’s tests ( n = 4 independent preparations). ( C ) HEK293T cells were transfected with either WT or CA CaMKIV and treated with CHX to inhibit further translation. Successively, cells were treated for 16 hours with DMSO (Veh), bafilomycin A1 (Baf; 100 nM; an inhibitor of lysosomal acidification and autophagy), leupeptin (Leu; 40 μM; an inhibitor of the lysosomal and cytosolic proteases), <t>CA074</t> (a specific inhibitor of Cathepsin B), or E64 (an inhibitor of cathepsins). Left: Representative immunoblots monitoring the expression of REST, calnexin, and the autophagy markers p62 and LC3B-I and -II. Right: Mean (±SEM) REST/calnexin ratios normalized with respect to the control REST/calnexin ratio in WT CaMKIV–expressing cells. Leu, * P = 0.0351; CA074, * P = 0.0361; E64, * P = 0.0481. Mixed-effects ANOVA/Dunnett’s tests ( n = 4 independent preparations).
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    ( A ) Schematics of the four possible degradation pathways that CaMKIV-phosphorylated REST can undertake and the three inhibitors that were used to dissect the fate of REST. Cat, cathepsin. ( B ) HEK293T cells were transfected with WT, CA, or KD CaMKIV and treated with cycloheximide (CHX) to in4hibit further translation. Then, cells were treated for 16 hours with either vehicle [dimethyl sulfoxide (DMSO)] or MG-132 (5 μM), an inhibitor of the ubiquitin-proteasome system (UPS). Left: Representative immunoblots monitoring the expression of WT, CA, and KD CaMKs, REST, and calnexin, respectively, in HEK293T cells, 48 hours after transfection with the kinase constructs. Right: Mean (±SEM) REST protein levels, shown as ratios with calnexin immunoreactivity under the various experimental conditions. No effects of inhibition of the UPS were observed. * P = 0.017, CA versus WT in DMSO; ** P = 0.0048, CA versus WT in MG-132. Two-way ANOVA/Tukey’s tests ( n = 4 independent preparations). ( C ) HEK293T cells were transfected with either WT or CA CaMKIV and treated with CHX to inhibit further translation. Successively, cells were treated for 16 hours with DMSO (Veh), bafilomycin A1 (Baf; 100 nM; an inhibitor of lysosomal acidification and autophagy), leupeptin (Leu; 40 μM; an inhibitor of the lysosomal and cytosolic proteases), <t>CA074</t> (a specific inhibitor of Cathepsin B), or E64 (an inhibitor of cathepsins). Left: Representative immunoblots monitoring the expression of REST, calnexin, and the autophagy markers p62 and LC3B-I and -II. Right: Mean (±SEM) REST/calnexin ratios normalized with respect to the control REST/calnexin ratio in WT CaMKIV–expressing cells. Leu, * P = 0.0351; CA074, * P = 0.0361; E64, * P = 0.0481. Mixed-effects ANOVA/Dunnett’s tests ( n = 4 independent preparations).
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    ( A ) Schematics of the four possible degradation pathways that CaMKIV-phosphorylated REST can undertake and the three inhibitors that were used to dissect the fate of REST. Cat, cathepsin. ( B ) HEK293T cells were transfected with WT, CA, or KD CaMKIV and treated with cycloheximide (CHX) to in4hibit further translation. Then, cells were treated for 16 hours with either vehicle [dimethyl sulfoxide (DMSO)] or MG-132 (5 μM), an inhibitor of the ubiquitin-proteasome system (UPS). Left: Representative immunoblots monitoring the expression of WT, CA, and KD CaMKs, REST, and calnexin, respectively, in HEK293T cells, 48 hours after transfection with the kinase constructs. Right: Mean (±SEM) REST protein levels, shown as ratios with calnexin immunoreactivity under the various experimental conditions. No effects of inhibition of the UPS were observed. * P = 0.017, CA versus WT in DMSO; ** P = 0.0048, CA versus WT in MG-132. Two-way ANOVA/Tukey’s tests ( n = 4 independent preparations). ( C ) HEK293T cells were transfected with either WT or CA CaMKIV and treated with CHX to inhibit further translation. Successively, cells were treated for 16 hours with DMSO (Veh), bafilomycin A1 (Baf; 100 nM; an inhibitor of lysosomal acidification and autophagy), leupeptin (Leu; 40 μM; an inhibitor of the lysosomal and cytosolic proteases), <t>CA074</t> (a specific inhibitor of Cathepsin B), or E64 (an inhibitor of cathepsins). Left: Representative immunoblots monitoring the expression of REST, calnexin, and the autophagy markers p62 and LC3B-I and -II. Right: Mean (±SEM) REST/calnexin ratios normalized with respect to the control REST/calnexin ratio in WT CaMKIV–expressing cells. Leu, * P = 0.0351; CA074, * P = 0.0361; E64, * P = 0.0481. Mixed-effects ANOVA/Dunnett’s tests ( n = 4 independent preparations).
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    ( A ) Schematics of the four possible degradation pathways that CaMKIV-phosphorylated REST can undertake and the three inhibitors that were used to dissect the fate of REST. Cat, cathepsin. ( B ) HEK293T cells were transfected with WT, CA, or KD CaMKIV and treated with cycloheximide (CHX) to in4hibit further translation. Then, cells were treated for 16 hours with either vehicle [dimethyl sulfoxide (DMSO)] or MG-132 (5 μM), an inhibitor of the ubiquitin-proteasome system (UPS). Left: Representative immunoblots monitoring the expression of WT, CA, and KD CaMKs, REST, and calnexin, respectively, in HEK293T cells, 48 hours after transfection with the kinase constructs. Right: Mean (±SEM) REST protein levels, shown as ratios with calnexin immunoreactivity under the various experimental conditions. No effects of inhibition of the UPS were observed. * P = 0.017, CA versus WT in DMSO; ** P = 0.0048, CA versus WT in MG-132. Two-way ANOVA/Tukey’s tests ( n = 4 independent preparations). ( C ) HEK293T cells were transfected with either WT or CA CaMKIV and treated with CHX to inhibit further translation. Successively, cells were treated for 16 hours with DMSO (Veh), bafilomycin A1 (Baf; 100 nM; an inhibitor of lysosomal acidification and autophagy), leupeptin (Leu; 40 μM; an inhibitor of the lysosomal and cytosolic proteases), <t>CA074</t> (a specific inhibitor of Cathepsin B), or E64 (an inhibitor of cathepsins). Left: Representative immunoblots monitoring the expression of REST, calnexin, and the autophagy markers p62 and LC3B-I and -II. Right: Mean (±SEM) REST/calnexin ratios normalized with respect to the control REST/calnexin ratio in WT CaMKIV–expressing cells. Leu, * P = 0.0351; CA074, * P = 0.0361; E64, * P = 0.0481. Mixed-effects ANOVA/Dunnett’s tests ( n = 4 independent preparations).
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    Image Search Results


    ( A ) Schematics of the four possible degradation pathways that CaMKIV-phosphorylated REST can undertake and the three inhibitors that were used to dissect the fate of REST. Cat, cathepsin. ( B ) HEK293T cells were transfected with WT, CA, or KD CaMKIV and treated with cycloheximide (CHX) to in4hibit further translation. Then, cells were treated for 16 hours with either vehicle [dimethyl sulfoxide (DMSO)] or MG-132 (5 μM), an inhibitor of the ubiquitin-proteasome system (UPS). Left: Representative immunoblots monitoring the expression of WT, CA, and KD CaMKs, REST, and calnexin, respectively, in HEK293T cells, 48 hours after transfection with the kinase constructs. Right: Mean (±SEM) REST protein levels, shown as ratios with calnexin immunoreactivity under the various experimental conditions. No effects of inhibition of the UPS were observed. * P = 0.017, CA versus WT in DMSO; ** P = 0.0048, CA versus WT in MG-132. Two-way ANOVA/Tukey’s tests ( n = 4 independent preparations). ( C ) HEK293T cells were transfected with either WT or CA CaMKIV and treated with CHX to inhibit further translation. Successively, cells were treated for 16 hours with DMSO (Veh), bafilomycin A1 (Baf; 100 nM; an inhibitor of lysosomal acidification and autophagy), leupeptin (Leu; 40 μM; an inhibitor of the lysosomal and cytosolic proteases), CA074 (a specific inhibitor of Cathepsin B), or E64 (an inhibitor of cathepsins). Left: Representative immunoblots monitoring the expression of REST, calnexin, and the autophagy markers p62 and LC3B-I and -II. Right: Mean (±SEM) REST/calnexin ratios normalized with respect to the control REST/calnexin ratio in WT CaMKIV–expressing cells. Leu, * P = 0.0351; CA074, * P = 0.0361; E64, * P = 0.0481. Mixed-effects ANOVA/Dunnett’s tests ( n = 4 independent preparations).

    Journal: Science Advances

    Article Title: Phosphorylation by CaMKIV regulates the transcriptional repressor activity and half-life of REST/NRSF

    doi: 10.1126/sciadv.aec0781

    Figure Lengend Snippet: ( A ) Schematics of the four possible degradation pathways that CaMKIV-phosphorylated REST can undertake and the three inhibitors that were used to dissect the fate of REST. Cat, cathepsin. ( B ) HEK293T cells were transfected with WT, CA, or KD CaMKIV and treated with cycloheximide (CHX) to in4hibit further translation. Then, cells were treated for 16 hours with either vehicle [dimethyl sulfoxide (DMSO)] or MG-132 (5 μM), an inhibitor of the ubiquitin-proteasome system (UPS). Left: Representative immunoblots monitoring the expression of WT, CA, and KD CaMKs, REST, and calnexin, respectively, in HEK293T cells, 48 hours after transfection with the kinase constructs. Right: Mean (±SEM) REST protein levels, shown as ratios with calnexin immunoreactivity under the various experimental conditions. No effects of inhibition of the UPS were observed. * P = 0.017, CA versus WT in DMSO; ** P = 0.0048, CA versus WT in MG-132. Two-way ANOVA/Tukey’s tests ( n = 4 independent preparations). ( C ) HEK293T cells were transfected with either WT or CA CaMKIV and treated with CHX to inhibit further translation. Successively, cells were treated for 16 hours with DMSO (Veh), bafilomycin A1 (Baf; 100 nM; an inhibitor of lysosomal acidification and autophagy), leupeptin (Leu; 40 μM; an inhibitor of the lysosomal and cytosolic proteases), CA074 (a specific inhibitor of Cathepsin B), or E64 (an inhibitor of cathepsins). Left: Representative immunoblots monitoring the expression of REST, calnexin, and the autophagy markers p62 and LC3B-I and -II. Right: Mean (±SEM) REST/calnexin ratios normalized with respect to the control REST/calnexin ratio in WT CaMKIV–expressing cells. Leu, * P = 0.0351; CA074, * P = 0.0361; E64, * P = 0.0481. Mixed-effects ANOVA/Dunnett’s tests ( n = 4 independent preparations).

    Article Snippet: W7, KN92, KN93, CA074, E64, bicuculline, CGP58845 , d -aminophosphovalerate, and tetrodotoxin were from Tocris (Bristol, UK).

    Techniques: Transfection, Ubiquitin Proteomics, Western Blot, Expressing, Construct, Inhibition, Control

    Limit of Detection of different HPV genotypes on the Steripack XpressCollect flocked nylon swab on the Atila ScreenFire HPV RS assay.

    Journal: Gates Open Research

    Article Title: Analytical performance and clinical usability of a low-cost vaginal swab for sensitive detection of high-risk human papillomavirus

    doi: 10.12688/gatesopenres.16399.1

    Figure Lengend Snippet: Limit of Detection of different HPV genotypes on the Steripack XpressCollect flocked nylon swab on the Atila ScreenFire HPV RS assay.

    Article Snippet: Human cervical cancer cell lines including SiHa (ATCC HTB-35), HeLa (ATCC CCL-2), CaSki (ATCC CRL-1550), and C-33A (ATCC HTB-31) cells from American Type Culture Collection (ATCC, Manassas, VA, USA) were grown at 37°C with 5% CO 2 in culture media: Dulbecco’s Modified Eagle Medium high glucose with sodium pyruvate containing 10% Fetal Bovine Serum (Gibco, Thermo Fisher Scientific, Waltham, MA, USA) and 50 μg/mL gentamycin (Sigma-Aldrich, St. Louis, MO, USA) under standard aseptic conditions while screening for mycoplasma contamination using the Universal Mycoplasma Detection kit (ATCC, Manassas, VA, USA) according to the manufacturer’s instructions.

    Techniques: Plasmid Preparation