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murine origin c2c12  (ATCC)


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    ATCC murine origin c2c12
    Effect of protein hydrolysate from silkworm pupae (SP) on <t>C2C12</t> myogenic differentiation: immunofluorescence assay. ( A ) C2C12 cells immunostained with anti-MyHC and DAPI were treated with different concentrations of SP (50, 100, 200, and 400 μg/mL); ( B ) the effect of SP on the fusion index for myotube formation; and ( C ) the My-HC positive cells were classified to mononucleus, 2–5 nuclei, and >5 nuclei. Three independent data were expressed as mean ± SD. Different superscripts indicate a significant difference ( p < 0.05).
    Murine Origin C2c12, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 8348 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/murine origin c2c12/product/ATCC
    Average 99 stars, based on 8348 article reviews
    murine origin c2c12 - by Bioz Stars, 2026-06
    99/100 stars

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    1) Product Images from "Effects of Protein Hydrolysate from Silkworm ( Bombyx mori ) pupae on the C2C12 Myogenic Differentiation"

    Article Title: Effects of Protein Hydrolysate from Silkworm ( Bombyx mori ) pupae on the C2C12 Myogenic Differentiation

    Journal: Foods

    doi: 10.3390/foods12152840

    Effect of protein hydrolysate from silkworm pupae (SP) on C2C12 myogenic differentiation: immunofluorescence assay. ( A ) C2C12 cells immunostained with anti-MyHC and DAPI were treated with different concentrations of SP (50, 100, 200, and 400 μg/mL); ( B ) the effect of SP on the fusion index for myotube formation; and ( C ) the My-HC positive cells were classified to mononucleus, 2–5 nuclei, and >5 nuclei. Three independent data were expressed as mean ± SD. Different superscripts indicate a significant difference ( p < 0.05).
    Figure Legend Snippet: Effect of protein hydrolysate from silkworm pupae (SP) on C2C12 myogenic differentiation: immunofluorescence assay. ( A ) C2C12 cells immunostained with anti-MyHC and DAPI were treated with different concentrations of SP (50, 100, 200, and 400 μg/mL); ( B ) the effect of SP on the fusion index for myotube formation; and ( C ) the My-HC positive cells were classified to mononucleus, 2–5 nuclei, and >5 nuclei. Three independent data were expressed as mean ± SD. Different superscripts indicate a significant difference ( p < 0.05).

    Techniques Used: Immunofluorescence

    Effect of fractionated protein hydrolysate from silkworm pupae (SP-Fs) on C2C12 myogenic differentiation: immunofluorescence assay. C2C12 cells immunostained with anti-MyHC and DAPI were treated with different concentrations of SP-Fs (50, 100, 200, and 400 μg/mL). ( A ), control; ( B ), SP-F1; ( C ), SP-F2; ( D ), SP-F3; ( E ), SP-F4; and ( F ), the effect of SP-Fs on the fusion index for myotube formation. Three independent data were expressed as mean ± SD. Different superscripts indicate a significant difference ( p < 0.05).
    Figure Legend Snippet: Effect of fractionated protein hydrolysate from silkworm pupae (SP-Fs) on C2C12 myogenic differentiation: immunofluorescence assay. C2C12 cells immunostained with anti-MyHC and DAPI were treated with different concentrations of SP-Fs (50, 100, 200, and 400 μg/mL). ( A ), control; ( B ), SP-F1; ( C ), SP-F2; ( D ), SP-F3; ( E ), SP-F4; and ( F ), the effect of SP-Fs on the fusion index for myotube formation. Three independent data were expressed as mean ± SD. Different superscripts indicate a significant difference ( p < 0.05).

    Techniques Used: Immunofluorescence, Control

    Effects of the subfraction 1 of silkworm pupae protein hydrolysate (SP-F1) on the expression of MyoD, myogenin, and MyHC of C2C12 myogenic differentiation. ( A ) Western blot analyses were performed to examine the expression of the myogenic regulatory factor proteins, namely MyoD ( B ), Myogenin ( C ), and MyHC ( D ), and their levels were quantified. Three independent data were expressed as mean ± SD. Different superscripts indicate a significant difference ( p < 0.05).
    Figure Legend Snippet: Effects of the subfraction 1 of silkworm pupae protein hydrolysate (SP-F1) on the expression of MyoD, myogenin, and MyHC of C2C12 myogenic differentiation. ( A ) Western blot analyses were performed to examine the expression of the myogenic regulatory factor proteins, namely MyoD ( B ), Myogenin ( C ), and MyHC ( D ), and their levels were quantified. Three independent data were expressed as mean ± SD. Different superscripts indicate a significant difference ( p < 0.05).

    Techniques Used: Expressing, Western Blot



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    murine origin c2c12  (ATCC)
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    ATCC murine origin c2c12
    Effect of protein hydrolysate from silkworm pupae (SP) on <t>C2C12</t> myogenic differentiation: immunofluorescence assay. ( A ) C2C12 cells immunostained with anti-MyHC and DAPI were treated with different concentrations of SP (50, 100, 200, and 400 μg/mL); ( B ) the effect of SP on the fusion index for myotube formation; and ( C ) the My-HC positive cells were classified to mononucleus, 2–5 nuclei, and >5 nuclei. Three independent data were expressed as mean ± SD. Different superscripts indicate a significant difference ( p < 0.05).
    Murine Origin C2c12, supplied by ATCC, 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/result/murine origin c2c12/product/ATCC
    Average 99 stars, based on 1 article reviews
    murine origin c2c12 - by Bioz Stars, 2026-06
    99/100 stars
    		  Buy from Supplier
    murine origin  (ATCC)
    99
    ATCC murine origin
    Effect of protein hydrolysate from silkworm pupae (SP) on <t>C2C12</t> myogenic differentiation: immunofluorescence assay. ( A ) C2C12 cells immunostained with anti-MyHC and DAPI were treated with different concentrations of SP (50, 100, 200, and 400 μg/mL); ( B ) the effect of SP on the fusion index for myotube formation; and ( C ) the My-HC positive cells were classified to mononucleus, 2–5 nuclei, and >5 nuclei. Three independent data were expressed as mean ± SD. Different superscripts indicate a significant difference ( p < 0.05).
    Murine Origin, supplied by ATCC, 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/result/murine origin/product/ATCC
    Average 99 stars, based on 1 article reviews
    murine origin - by Bioz Stars, 2026-06
    99/100 stars
    		  Buy from Supplier

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    Effect of protein hydrolysate from silkworm pupae (SP) on C2C12 myogenic differentiation: immunofluorescence assay. ( A ) C2C12 cells immunostained with anti-MyHC and DAPI were treated with different concentrations of SP (50, 100, 200, and 400 μg/mL); ( B ) the effect of SP on the fusion index for myotube formation; and ( C ) the My-HC positive cells were classified to mononucleus, 2–5 nuclei, and >5 nuclei. Three independent data were expressed as mean ± SD. Different superscripts indicate a significant difference ( p < 0.05).

    Journal: Foods

    Article Title: Effects of Protein Hydrolysate from Silkworm ( Bombyx mori ) pupae on the C2C12 Myogenic Differentiation

    doi: 10.3390/foods12152840

    Figure Lengend Snippet: Effect of protein hydrolysate from silkworm pupae (SP) on C2C12 myogenic differentiation: immunofluorescence assay. ( A ) C2C12 cells immunostained with anti-MyHC and DAPI were treated with different concentrations of SP (50, 100, 200, and 400 μg/mL); ( B ) the effect of SP on the fusion index for myotube formation; and ( C ) the My-HC positive cells were classified to mononucleus, 2–5 nuclei, and >5 nuclei. Three independent data were expressed as mean ± SD. Different superscripts indicate a significant difference ( p < 0.05).

    Article Snippet: Murine-origin C2C12 (ATCC, Manassas, VA, USA) myoblast cells were seeded in a 10 cm cell culture dish at a cell density of 3 × 10 5 .

    Techniques: Immunofluorescence

    Effect of fractionated protein hydrolysate from silkworm pupae (SP-Fs) on C2C12 myogenic differentiation: immunofluorescence assay. C2C12 cells immunostained with anti-MyHC and DAPI were treated with different concentrations of SP-Fs (50, 100, 200, and 400 μg/mL). ( A ), control; ( B ), SP-F1; ( C ), SP-F2; ( D ), SP-F3; ( E ), SP-F4; and ( F ), the effect of SP-Fs on the fusion index for myotube formation. Three independent data were expressed as mean ± SD. Different superscripts indicate a significant difference ( p < 0.05).

    Journal: Foods

    Article Title: Effects of Protein Hydrolysate from Silkworm ( Bombyx mori ) pupae on the C2C12 Myogenic Differentiation

    doi: 10.3390/foods12152840

    Figure Lengend Snippet: Effect of fractionated protein hydrolysate from silkworm pupae (SP-Fs) on C2C12 myogenic differentiation: immunofluorescence assay. C2C12 cells immunostained with anti-MyHC and DAPI were treated with different concentrations of SP-Fs (50, 100, 200, and 400 μg/mL). ( A ), control; ( B ), SP-F1; ( C ), SP-F2; ( D ), SP-F3; ( E ), SP-F4; and ( F ), the effect of SP-Fs on the fusion index for myotube formation. Three independent data were expressed as mean ± SD. Different superscripts indicate a significant difference ( p < 0.05).

    Article Snippet: Murine-origin C2C12 (ATCC, Manassas, VA, USA) myoblast cells were seeded in a 10 cm cell culture dish at a cell density of 3 × 10 5 .

    Techniques: Immunofluorescence, Control

    Effects of the subfraction 1 of silkworm pupae protein hydrolysate (SP-F1) on the expression of MyoD, myogenin, and MyHC of C2C12 myogenic differentiation. ( A ) Western blot analyses were performed to examine the expression of the myogenic regulatory factor proteins, namely MyoD ( B ), Myogenin ( C ), and MyHC ( D ), and their levels were quantified. Three independent data were expressed as mean ± SD. Different superscripts indicate a significant difference ( p < 0.05).

    Journal: Foods

    Article Title: Effects of Protein Hydrolysate from Silkworm ( Bombyx mori ) pupae on the C2C12 Myogenic Differentiation

    doi: 10.3390/foods12152840

    Figure Lengend Snippet: Effects of the subfraction 1 of silkworm pupae protein hydrolysate (SP-F1) on the expression of MyoD, myogenin, and MyHC of C2C12 myogenic differentiation. ( A ) Western blot analyses were performed to examine the expression of the myogenic regulatory factor proteins, namely MyoD ( B ), Myogenin ( C ), and MyHC ( D ), and their levels were quantified. Three independent data were expressed as mean ± SD. Different superscripts indicate a significant difference ( p < 0.05).

    Article Snippet: Murine-origin C2C12 (ATCC, Manassas, VA, USA) myoblast cells were seeded in a 10 cm cell culture dish at a cell density of 3 × 10 5 .

    Techniques: Expressing, Western Blot