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staphylococcus aureus subsp. aureus rosenbach  (ATCC)


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    ATCC staphylococcus aureus subsp. aureus rosenbach
    Staphylococcus Aureus Subsp. Aureus Rosenbach, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 16090 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/c++/Staphylococcus+aureus+subsp%2E+aureus+Rosenbach/custom%406538%4042906997
    Average 99 stars, based on 16090 article reviews
    staphylococcus aureus subsp. aureus rosenbach - by Bioz Stars, 2026-11
    99/100 stars

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    Related Articles

    Irradiation:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in

    Incubation:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in

    Cell Culture:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in

    Concentration Assay:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in

    Recombinant:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in

    Plasmid Preparation:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in

    Modification:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in

    Selection:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in

    Synthesized:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in

    Control:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in

    QC/EQA/Proficiency:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in

    Illumina Sequencing:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in

    Polymerase Chain Reaction:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in

    Sequencing:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in

    cDNA Synthesis:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in

    Amplification:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in

    Activity Assay:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in



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    Image Search Results


    Voluntary exercise alters left ventricle gene and protein expression related to mitochondrial biogenesis and dynamics in high fat- and chow-fed mice. (A) Western blot analysis to assess purity of crude mitochondria isolation where left ventricle mitochondrial pellet expresses mitochondrial marker TOM70 and COXIV and supernatant expresses calnexin. Protein expression of (B) LCLAT1 and (C) MFN2 in left ventricle-isolated crude mitochondria and (D) LCLAT1, (E) PGC-1α, and (F) MFN2 in left ventricle tissue from male VET or sedentary mice fed an HFD or chow diet. Left ventricle mRNA expression of (G) OPA1 and (H) DRP1 in male VET or sedentary mice fed an HFD or chow diet. Values were calculated relative to 18S housekeeper. Calnexin and β-actin were used as internal controls of protein loading in left ventricle samples and COXIV as internal control of protein loading in crude mitochondria samples. Analysis was performed using two-way analysis of variance with Tukey’s post hoc test for multiple comparisons. Data are expressed as mean ± standard error of the mean. (B–C) n : 5–6 per group. (D–F) n = 7 per group. (G and H) n = 9 per group. CE = chow exercise; CS = chow sedentary; COXIV = cytochrome c oxidase subunit 4; DRP1 = dynamin-related protein 1; HE = high fat diet exercise; HFD = high fat diet; HS = high fat diet sedentary; LCLAT1 = lysocardiolipin acyltransferase 1; MFN2 = mitofusin-2; OPA1 = optic atrophy 1; PGC-1α = peroxisome proliferator-activated receptor gamma coactivator-1α; TOM70 = translocase of outer mitochondria membrane 70; VET = voluntary exercise training.

    Journal: Journal of Sport and Health Science

    Article Title: Influence of diet-induced obesity and voluntary exercise training on cardiac lipids and mitochondrial function in mice

    doi: 10.1016/j.jshs.2025.101095

    Figure Lengend Snippet: Voluntary exercise alters left ventricle gene and protein expression related to mitochondrial biogenesis and dynamics in high fat- and chow-fed mice. (A) Western blot analysis to assess purity of crude mitochondria isolation where left ventricle mitochondrial pellet expresses mitochondrial marker TOM70 and COXIV and supernatant expresses calnexin. Protein expression of (B) LCLAT1 and (C) MFN2 in left ventricle-isolated crude mitochondria and (D) LCLAT1, (E) PGC-1α, and (F) MFN2 in left ventricle tissue from male VET or sedentary mice fed an HFD or chow diet. Left ventricle mRNA expression of (G) OPA1 and (H) DRP1 in male VET or sedentary mice fed an HFD or chow diet. Values were calculated relative to 18S housekeeper. Calnexin and β-actin were used as internal controls of protein loading in left ventricle samples and COXIV as internal control of protein loading in crude mitochondria samples. Analysis was performed using two-way analysis of variance with Tukey’s post hoc test for multiple comparisons. Data are expressed as mean ± standard error of the mean. (B–C) n : 5–6 per group. (D–F) n = 7 per group. (G and H) n = 9 per group. CE = chow exercise; CS = chow sedentary; COXIV = cytochrome c oxidase subunit 4; DRP1 = dynamin-related protein 1; HE = high fat diet exercise; HFD = high fat diet; HS = high fat diet sedentary; LCLAT1 = lysocardiolipin acyltransferase 1; MFN2 = mitofusin-2; OPA1 = optic atrophy 1; PGC-1α = peroxisome proliferator-activated receptor gamma coactivator-1α; TOM70 = translocase of outer mitochondria membrane 70; VET = voluntary exercise training.

    Article Snippet: The plate was centrifuged at 500 g for 5 min at 4°C, and 140 μL of MAS buffer containing 10 μg/mL cytochrome C (Thermo Fisher Scientific) was pipetted to each well.

    Techniques: Expressing, Western Blot, Isolation, Marker, Control, Membrane

    Voluntary exercise alters left ventricle gene and protein expression related to mitochondrial biogenesis and dynamics in high fat- and chow-fed mice. (A) Western blot analysis to assess purity of crude mitochondria isolation where left ventricle mitochondrial pellet expresses mitochondrial marker TOM70 and COXIV and supernatant expresses calnexin. Protein expression of (B) LCLAT1 and (C) MFN2 in left ventricle-isolated crude mitochondria and (D) LCLAT1, (E) PGC-1α, and (F) MFN2 in left ventricle tissue from male VET or sedentary mice fed an HFD or chow diet. Left ventricle mRNA expression of (G) OPA1 and (H) DRP1 in male VET or sedentary mice fed an HFD or chow diet. Values were calculated relative to 18S housekeeper. Calnexin and β-actin were used as internal controls of protein loading in left ventricle samples and COXIV as internal control of protein loading in crude mitochondria samples. Analysis was performed using two-way analysis of variance with Tukey’s post hoc test for multiple comparisons. Data are expressed as mean ± standard error of the mean. (B–C) n : 5–6 per group. (D–F) n = 7 per group. (G and H) n = 9 per group. CE = chow exercise; CS = chow sedentary; COXIV = cytochrome c oxidase subunit 4; DRP1 = dynamin-related protein 1; HE = high fat diet exercise; HFD = high fat diet; HS = high fat diet sedentary; LCLAT1 = lysocardiolipin acyltransferase 1; MFN2 = mitofusin-2; OPA1 = optic atrophy 1; PGC-1α = peroxisome proliferator-activated receptor gamma coactivator-1α; TOM70 = translocase of outer mitochondria membrane 70; VET = voluntary exercise training.

    Journal: Journal of Sport and Health Science

    Article Title: Influence of diet-induced obesity and voluntary exercise training on cardiac lipids and mitochondrial function in mice

    doi: 10.1016/j.jshs.2025.101095

    Figure Lengend Snippet: Voluntary exercise alters left ventricle gene and protein expression related to mitochondrial biogenesis and dynamics in high fat- and chow-fed mice. (A) Western blot analysis to assess purity of crude mitochondria isolation where left ventricle mitochondrial pellet expresses mitochondrial marker TOM70 and COXIV and supernatant expresses calnexin. Protein expression of (B) LCLAT1 and (C) MFN2 in left ventricle-isolated crude mitochondria and (D) LCLAT1, (E) PGC-1α, and (F) MFN2 in left ventricle tissue from male VET or sedentary mice fed an HFD or chow diet. Left ventricle mRNA expression of (G) OPA1 and (H) DRP1 in male VET or sedentary mice fed an HFD or chow diet. Values were calculated relative to 18S housekeeper. Calnexin and β-actin were used as internal controls of protein loading in left ventricle samples and COXIV as internal control of protein loading in crude mitochondria samples. Analysis was performed using two-way analysis of variance with Tukey’s post hoc test for multiple comparisons. Data are expressed as mean ± standard error of the mean. (B–C) n : 5–6 per group. (D–F) n = 7 per group. (G and H) n = 9 per group. CE = chow exercise; CS = chow sedentary; COXIV = cytochrome c oxidase subunit 4; DRP1 = dynamin-related protein 1; HE = high fat diet exercise; HFD = high fat diet; HS = high fat diet sedentary; LCLAT1 = lysocardiolipin acyltransferase 1; MFN2 = mitofusin-2; OPA1 = optic atrophy 1; PGC-1α = peroxisome proliferator-activated receptor gamma coactivator-1α; TOM70 = translocase of outer mitochondria membrane 70; VET = voluntary exercise training.

    Article Snippet: Immunoblotting was performed with antibodies against lysocardiolipin acyltransferase 1(LCLAT1, PA5-25627; Thermo Fisher Scientific), PGC-1α (ab191838; Abcam, Cambridge, UK), MFN2 (PA5-118059; Thermo Fisher Scientific), ANP (sc-18811; Santa Cruz, Dallas, TX, USA), tumor necrosis factor alpha (TNFα, 3707; Cell Signaling, Danvers, MA, USA), phosphorylated adenosine monophosphate-activated protein kinase (AMPK, 2531; Cell Signaling), AMPKα (2532; Cell Signaling), Perilipin 5 (PA1-46215; Thermo Fisher Scientific), translocase of outer mitochondria membrane 70 (TOM70, 65675; Cell Signaling), cytochrome c oxidase subunit 4 (COXIV, 4844; Cell Signaling), and calnexin (208880; Merck, Rahway, NJ, USA).

    Techniques: Expressing, Western Blot, Isolation, Marker, Control, Membrane