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human skeletal muscle cell differentiation medium  (Cell Applications Inc)


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    Cell Applications Inc human skeletal muscle cell differentiation medium
    Human Skeletal Muscle Cell Differentiation Medium, supplied by Cell Applications Inc, used in various techniques. Bioz Stars score: 92/100, based on 12 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human skeletal muscle cell differentiation medium/product/Cell Applications Inc
    Average 92 stars, based on 12 article reviews
    human skeletal muscle cell differentiation medium - by Bioz Stars, 2026-02
    92/100 stars

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    ( A , B ) Representative immunoblot ( n = 4–6) of immunoprecipitates (IP) of CHC22, from control HeLa cells ( A ) and differentiated human skeletal muscle cell line <t>AB1190</t> (Myotubes) ( B ). Samples were immunoblotted for CHC22, SNX5, SNX6, and tubulin. Lanes show Input (5%), bead-only (no antibody) control (Bead) and CHC22 immunoprecipitate (22 IP). The migration positions of MW markers are indicated at the left in kilodaltons (kD). ( C ) The structure of a single clathrin triskelion formed from three clathrin heavy chains with the Hub region indicated by red dotted triangle and the trimerization domain (TxD), magenta), proximal leg region (dark blue), knee and distal leg regions (grey) and terminal domain (light blue), based on PDB 31YV (Fotin et al, ). ( D ) AlphaFold-generated model of the interaction between CHC22 Hub (blue proximal leg residues 1278–1519 and magenta TxD residues 1520–1640) and the BAR domain of SNX5 (residues 202–404, orange). Two angles of view are displayed. ( E ) Representative immunoblot ( n = 3–5) of in vitro binding of full-length GST-SNX5 (right lanes) or GST alone (left lanes) to CHC22 Hub (22 Hub) or CHC17 Hub (17 Hub) immobilized on Ni-NTA beads. Purified protein input (2%) and bead-only (no Hub immobilized) control (Bead) are shown for each prey. Samples were immunoblotted for SNX5, His-tag or GST with detected proteins indicated at the right. The position of MW markers is indicated at the left in kD. (F) Representative immunoblot of in vitro binding of full-length GST-SNX5 (right lanes) or GST alone (left lanes) to CHC22 Hub or CHC22 TxD immobilized on Ni-NTA beads ( n = 3). Purified protein input (2%) and beads without CHC22 fragment added (Bead) are shown for each prey. Samples were immunoblotted for SNX5, His-tag or GST with detected proteins indicated at the right. The position of MW markers is indicated at the left in kD. .
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    ( A , B ) Representative immunoblot ( n = 4–6) of immunoprecipitates (IP) of CHC22, from control HeLa cells ( A ) and differentiated human skeletal muscle cell line <t>AB1190</t> (Myotubes) ( B ). Samples were immunoblotted for CHC22, SNX5, SNX6, and tubulin. Lanes show Input (5%), bead-only (no antibody) control (Bead) and CHC22 immunoprecipitate (22 IP). The migration positions of MW markers are indicated at the left in kilodaltons (kD). ( C ) The structure of a single clathrin triskelion formed from three clathrin heavy chains with the Hub region indicated by red dotted triangle and the trimerization domain (TxD), magenta), proximal leg region (dark blue), knee and distal leg regions (grey) and terminal domain (light blue), based on PDB 31YV (Fotin et al, ). ( D ) AlphaFold-generated model of the interaction between CHC22 Hub (blue proximal leg residues 1278–1519 and magenta TxD residues 1520–1640) and the BAR domain of SNX5 (residues 202–404, orange). Two angles of view are displayed. ( E ) Representative immunoblot ( n = 3–5) of in vitro binding of full-length GST-SNX5 (right lanes) or GST alone (left lanes) to CHC22 Hub (22 Hub) or CHC17 Hub (17 Hub) immobilized on Ni-NTA beads. Purified protein input (2%) and bead-only (no Hub immobilized) control (Bead) are shown for each prey. Samples were immunoblotted for SNX5, His-tag or GST with detected proteins indicated at the right. The position of MW markers is indicated at the left in kD. (F) Representative immunoblot of in vitro binding of full-length GST-SNX5 (right lanes) or GST alone (left lanes) to CHC22 Hub or CHC22 TxD immobilized on Ni-NTA beads ( n = 3). Purified protein input (2%) and beads without CHC22 fragment added (Bead) are shown for each prey. Samples were immunoblotted for SNX5, His-tag or GST with detected proteins indicated at the right. The position of MW markers is indicated at the left in kD. .
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    skeletal muscle cell basal medium  (Cell Applications Inc)
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    ( A , B ) Representative immunoblot ( n = 4–6) of immunoprecipitates (IP) of CHC22, from control HeLa cells ( A ) and differentiated human skeletal muscle cell line <t>AB1190</t> (Myotubes) ( B ). Samples were immunoblotted for CHC22, SNX5, SNX6, and tubulin. Lanes show Input (5%), bead-only (no antibody) control (Bead) and CHC22 immunoprecipitate (22 IP). The migration positions of MW markers are indicated at the left in kilodaltons (kD). ( C ) The structure of a single clathrin triskelion formed from three clathrin heavy chains with the Hub region indicated by red dotted triangle and the trimerization domain (TxD), magenta), proximal leg region (dark blue), knee and distal leg regions (grey) and terminal domain (light blue), based on PDB 31YV (Fotin et al, ). ( D ) AlphaFold-generated model of the interaction between CHC22 Hub (blue proximal leg residues 1278–1519 and magenta TxD residues 1520–1640) and the BAR domain of SNX5 (residues 202–404, orange). Two angles of view are displayed. ( E ) Representative immunoblot ( n = 3–5) of in vitro binding of full-length GST-SNX5 (right lanes) or GST alone (left lanes) to CHC22 Hub (22 Hub) or CHC17 Hub (17 Hub) immobilized on Ni-NTA beads. Purified protein input (2%) and bead-only (no Hub immobilized) control (Bead) are shown for each prey. Samples were immunoblotted for SNX5, His-tag or GST with detected proteins indicated at the right. The position of MW markers is indicated at the left in kD. (F) Representative immunoblot of in vitro binding of full-length GST-SNX5 (right lanes) or GST alone (left lanes) to CHC22 Hub or CHC22 TxD immobilized on Ni-NTA beads ( n = 3). Purified protein input (2%) and beads without CHC22 fragment added (Bead) are shown for each prey. Samples were immunoblotted for SNX5, His-tag or GST with detected proteins indicated at the right. The position of MW markers is indicated at the left in kD. .
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    ( A , B ) Representative immunoblot ( n = 4–6) of immunoprecipitates (IP) of CHC22, from control HeLa cells ( A ) and differentiated human skeletal muscle cell line <t>AB1190</t> (Myotubes) ( B ). Samples were immunoblotted for CHC22, SNX5, SNX6, and tubulin. Lanes show Input (5%), bead-only (no antibody) control (Bead) and CHC22 immunoprecipitate (22 IP). The migration positions of MW markers are indicated at the left in kilodaltons (kD). ( C ) The structure of a single clathrin triskelion formed from three clathrin heavy chains with the Hub region indicated by red dotted triangle and the trimerization domain (TxD), magenta), proximal leg region (dark blue), knee and distal leg regions (grey) and terminal domain (light blue), based on PDB 31YV (Fotin et al, ). ( D ) AlphaFold-generated model of the interaction between CHC22 Hub (blue proximal leg residues 1278–1519 and magenta TxD residues 1520–1640) and the BAR domain of SNX5 (residues 202–404, orange). Two angles of view are displayed. ( E ) Representative immunoblot ( n = 3–5) of in vitro binding of full-length GST-SNX5 (right lanes) or GST alone (left lanes) to CHC22 Hub (22 Hub) or CHC17 Hub (17 Hub) immobilized on Ni-NTA beads. Purified protein input (2%) and bead-only (no Hub immobilized) control (Bead) are shown for each prey. Samples were immunoblotted for SNX5, His-tag or GST with detected proteins indicated at the right. The position of MW markers is indicated at the left in kD. (F) Representative immunoblot of in vitro binding of full-length GST-SNX5 (right lanes) or GST alone (left lanes) to CHC22 Hub or CHC22 TxD immobilized on Ni-NTA beads ( n = 3). Purified protein input (2%) and beads without CHC22 fragment added (Bead) are shown for each prey. Samples were immunoblotted for SNX5, His-tag or GST with detected proteins indicated at the right. The position of MW markers is indicated at the left in kD. .
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    https://www.bioz.com/result/skeletal muscle differentiation medium/product/Cell Applications Inc
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    skeletal muscle differentiation medium - by Bioz Stars, 2026-02
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    skeletal muscle cell differentiation medium  (Cell Applications Inc)
    92
    Cell Applications Inc skeletal muscle cell differentiation medium
    ( A , B ) Representative immunoblot ( n = 4–6) of immunoprecipitates (IP) of CHC22, from control HeLa cells ( A ) and differentiated human skeletal muscle cell line <t>AB1190</t> (Myotubes) ( B ). Samples were immunoblotted for CHC22, SNX5, SNX6, and tubulin. Lanes show Input (5%), bead-only (no antibody) control (Bead) and CHC22 immunoprecipitate (22 IP). The migration positions of MW markers are indicated at the left in kilodaltons (kD). ( C ) The structure of a single clathrin triskelion formed from three clathrin heavy chains with the Hub region indicated by red dotted triangle and the trimerization domain (TxD), magenta), proximal leg region (dark blue), knee and distal leg regions (grey) and terminal domain (light blue), based on PDB 31YV (Fotin et al, ). ( D ) AlphaFold-generated model of the interaction between CHC22 Hub (blue proximal leg residues 1278–1519 and magenta TxD residues 1520–1640) and the BAR domain of SNX5 (residues 202–404, orange). Two angles of view are displayed. ( E ) Representative immunoblot ( n = 3–5) of in vitro binding of full-length GST-SNX5 (right lanes) or GST alone (left lanes) to CHC22 Hub (22 Hub) or CHC17 Hub (17 Hub) immobilized on Ni-NTA beads. Purified protein input (2%) and bead-only (no Hub immobilized) control (Bead) are shown for each prey. Samples were immunoblotted for SNX5, His-tag or GST with detected proteins indicated at the right. The position of MW markers is indicated at the left in kD. (F) Representative immunoblot of in vitro binding of full-length GST-SNX5 (right lanes) or GST alone (left lanes) to CHC22 Hub or CHC22 TxD immobilized on Ni-NTA beads ( n = 3). Purified protein input (2%) and beads without CHC22 fragment added (Bead) are shown for each prey. Samples were immunoblotted for SNX5, His-tag or GST with detected proteins indicated at the right. The position of MW markers is indicated at the left in kD. .
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    skeletal muscle cell growth medium  (Cell Applications Inc)
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    Cell Applications Inc skeletal muscle cell growth medium
    ( A , B ) Representative immunoblot ( n = 4–6) of immunoprecipitates (IP) of CHC22, from control HeLa cells ( A ) and differentiated human skeletal muscle cell line <t>AB1190</t> (Myotubes) ( B ). Samples were immunoblotted for CHC22, SNX5, SNX6, and tubulin. Lanes show Input (5%), bead-only (no antibody) control (Bead) and CHC22 immunoprecipitate (22 IP). The migration positions of MW markers are indicated at the left in kilodaltons (kD). ( C ) The structure of a single clathrin triskelion formed from three clathrin heavy chains with the Hub region indicated by red dotted triangle and the trimerization domain (TxD), magenta), proximal leg region (dark blue), knee and distal leg regions (grey) and terminal domain (light blue), based on PDB 31YV (Fotin et al, ). ( D ) AlphaFold-generated model of the interaction between CHC22 Hub (blue proximal leg residues 1278–1519 and magenta TxD residues 1520–1640) and the BAR domain of SNX5 (residues 202–404, orange). Two angles of view are displayed. ( E ) Representative immunoblot ( n = 3–5) of in vitro binding of full-length GST-SNX5 (right lanes) or GST alone (left lanes) to CHC22 Hub (22 Hub) or CHC17 Hub (17 Hub) immobilized on Ni-NTA beads. Purified protein input (2%) and bead-only (no Hub immobilized) control (Bead) are shown for each prey. Samples were immunoblotted for SNX5, His-tag or GST with detected proteins indicated at the right. The position of MW markers is indicated at the left in kD. (F) Representative immunoblot of in vitro binding of full-length GST-SNX5 (right lanes) or GST alone (left lanes) to CHC22 Hub or CHC22 TxD immobilized on Ni-NTA beads ( n = 3). Purified protein input (2%) and beads without CHC22 fragment added (Bead) are shown for each prey. Samples were immunoblotted for SNX5, His-tag or GST with detected proteins indicated at the right. The position of MW markers is indicated at the left in kD. .
    Skeletal Muscle Cell Growth Medium, supplied by Cell Applications Inc, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/skeletal muscle cell growth medium/product/Cell Applications Inc
    Average 92 stars, based on 1 article reviews
    skeletal muscle cell growth medium - by Bioz Stars, 2026-02
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    ( A , B ) Representative immunoblot ( n = 4–6) of immunoprecipitates (IP) of CHC22, from control HeLa cells ( A ) and differentiated human skeletal muscle cell line AB1190 (Myotubes) ( B ). Samples were immunoblotted for CHC22, SNX5, SNX6, and tubulin. Lanes show Input (5%), bead-only (no antibody) control (Bead) and CHC22 immunoprecipitate (22 IP). The migration positions of MW markers are indicated at the left in kilodaltons (kD). ( C ) The structure of a single clathrin triskelion formed from three clathrin heavy chains with the Hub region indicated by red dotted triangle and the trimerization domain (TxD), magenta), proximal leg region (dark blue), knee and distal leg regions (grey) and terminal domain (light blue), based on PDB 31YV (Fotin et al, ). ( D ) AlphaFold-generated model of the interaction between CHC22 Hub (blue proximal leg residues 1278–1519 and magenta TxD residues 1520–1640) and the BAR domain of SNX5 (residues 202–404, orange). Two angles of view are displayed. ( E ) Representative immunoblot ( n = 3–5) of in vitro binding of full-length GST-SNX5 (right lanes) or GST alone (left lanes) to CHC22 Hub (22 Hub) or CHC17 Hub (17 Hub) immobilized on Ni-NTA beads. Purified protein input (2%) and bead-only (no Hub immobilized) control (Bead) are shown for each prey. Samples were immunoblotted for SNX5, His-tag or GST with detected proteins indicated at the right. The position of MW markers is indicated at the left in kD. (F) Representative immunoblot of in vitro binding of full-length GST-SNX5 (right lanes) or GST alone (left lanes) to CHC22 Hub or CHC22 TxD immobilized on Ni-NTA beads ( n = 3). Purified protein input (2%) and beads without CHC22 fragment added (Bead) are shown for each prey. Samples were immunoblotted for SNX5, His-tag or GST with detected proteins indicated at the right. The position of MW markers is indicated at the left in kD. .

    Journal: The EMBO Journal

    Article Title: CHC22 clathrin recruitment to the early secretory pathway requires two-site interaction with SNX5 and p115

    doi: 10.1038/s44318-024-00198-y

    Figure Lengend Snippet: ( A , B ) Representative immunoblot ( n = 4–6) of immunoprecipitates (IP) of CHC22, from control HeLa cells ( A ) and differentiated human skeletal muscle cell line AB1190 (Myotubes) ( B ). Samples were immunoblotted for CHC22, SNX5, SNX6, and tubulin. Lanes show Input (5%), bead-only (no antibody) control (Bead) and CHC22 immunoprecipitate (22 IP). The migration positions of MW markers are indicated at the left in kilodaltons (kD). ( C ) The structure of a single clathrin triskelion formed from three clathrin heavy chains with the Hub region indicated by red dotted triangle and the trimerization domain (TxD), magenta), proximal leg region (dark blue), knee and distal leg regions (grey) and terminal domain (light blue), based on PDB 31YV (Fotin et al, ). ( D ) AlphaFold-generated model of the interaction between CHC22 Hub (blue proximal leg residues 1278–1519 and magenta TxD residues 1520–1640) and the BAR domain of SNX5 (residues 202–404, orange). Two angles of view are displayed. ( E ) Representative immunoblot ( n = 3–5) of in vitro binding of full-length GST-SNX5 (right lanes) or GST alone (left lanes) to CHC22 Hub (22 Hub) or CHC17 Hub (17 Hub) immobilized on Ni-NTA beads. Purified protein input (2%) and bead-only (no Hub immobilized) control (Bead) are shown for each prey. Samples were immunoblotted for SNX5, His-tag or GST with detected proteins indicated at the right. The position of MW markers is indicated at the left in kD. (F) Representative immunoblot of in vitro binding of full-length GST-SNX5 (right lanes) or GST alone (left lanes) to CHC22 Hub or CHC22 TxD immobilized on Ni-NTA beads ( n = 3). Purified protein input (2%) and beads without CHC22 fragment added (Bead) are shown for each prey. Samples were immunoblotted for SNX5, His-tag or GST with detected proteins indicated at the right. The position of MW markers is indicated at the left in kD. .

    Article Snippet: The human myoblast cell line AB1190 was grown in complete Skeletal Muscle Cell Growth Medium (Promocell) with provided supplemental cocktail and 10% FBS (Gibco) to reach a 15% final supplement concentration (volume/volume) (Camus et al, ).

    Techniques: Western Blot, Control, Migration, Generated, In Vitro, Binding Assay, Purification