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fluorchemq multiimage iii instrument  (Alpha Innotech)

 
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    Alpha Innotech fluorchemq multiimage iii instrument
    Western blot validation of host protein regulation. A , HeLa cells were mock-infected or infected for 24 h, or B , for indicated periods of time, harvested and lysed with 0.5% NP-40 detergent. The cytosolic and nuclear fractions were separately purified, dissolved in SDS electrophoresis sample buffer, and proteins resolved in 10% ( A ), or in 4-16% gradient ( B ) SDS-PAGE, transferred to PVDF, and probed with indicated antibodies. Antibody binding was detected with HRP-conjugated secondary antibodies and ECL, and visualized with an Alpha Innotech <t>FluorChemQ</t> <t>MultiImage</t> <t>III</t> instrument. Molecular weight standards are indicated at left and SILAC-measured ratios are indicated on right in A . *: not detected in indicated fraction; †: based on single peptide only.
    Fluorchemq Multiimage Iii Instrument, supplied by Alpha Innotech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/fluorchemq multiimage iii instrument/product/Alpha Innotech
    Average 90 stars, based on 1 article reviews
    fluorchemq multiimage iii instrument - by Bioz Stars, 2026-03
    90/100 stars

    Images

    1) Product Images from "HeLa cell response proteome alterations induced by mammalian reovirus T3D infection"

    Article Title: HeLa cell response proteome alterations induced by mammalian reovirus T3D infection

    Journal: Virology Journal

    doi: 10.1186/1743-422X-10-202

    Western blot validation of host protein regulation. A , HeLa cells were mock-infected or infected for 24 h, or B , for indicated periods of time, harvested and lysed with 0.5% NP-40 detergent. The cytosolic and nuclear fractions were separately purified, dissolved in SDS electrophoresis sample buffer, and proteins resolved in 10% ( A ), or in 4-16% gradient ( B ) SDS-PAGE, transferred to PVDF, and probed with indicated antibodies. Antibody binding was detected with HRP-conjugated secondary antibodies and ECL, and visualized with an Alpha Innotech FluorChemQ MultiImage III instrument. Molecular weight standards are indicated at left and SILAC-measured ratios are indicated on right in A . *: not detected in indicated fraction; †: based on single peptide only.
    Figure Legend Snippet: Western blot validation of host protein regulation. A , HeLa cells were mock-infected or infected for 24 h, or B , for indicated periods of time, harvested and lysed with 0.5% NP-40 detergent. The cytosolic and nuclear fractions were separately purified, dissolved in SDS electrophoresis sample buffer, and proteins resolved in 10% ( A ), or in 4-16% gradient ( B ) SDS-PAGE, transferred to PVDF, and probed with indicated antibodies. Antibody binding was detected with HRP-conjugated secondary antibodies and ECL, and visualized with an Alpha Innotech FluorChemQ MultiImage III instrument. Molecular weight standards are indicated at left and SILAC-measured ratios are indicated on right in A . *: not detected in indicated fraction; †: based on single peptide only.

    Techniques Used: Western Blot, Infection, Purification, Electrophoresis, SDS Page, Binding Assay, Molecular Weight



    Similar Products

    fluorchemq multiimage iii instrument  (Alpha Innotech)
    90
    Alpha Innotech fluorchemq multiimage iii instrument
    Western blot validation of host protein regulation. A , HeLa cells were mock-infected or infected for 24 h, or B , for indicated periods of time, harvested and lysed with 0.5% NP-40 detergent. The cytosolic and nuclear fractions were separately purified, dissolved in SDS electrophoresis sample buffer, and proteins resolved in 10% ( A ), or in 4-16% gradient ( B ) SDS-PAGE, transferred to PVDF, and probed with indicated antibodies. Antibody binding was detected with HRP-conjugated secondary antibodies and ECL, and visualized with an Alpha Innotech <t>FluorChemQ</t> <t>MultiImage</t> <t>III</t> instrument. Molecular weight standards are indicated at left and SILAC-measured ratios are indicated on right in A . *: not detected in indicated fraction; †: based on single peptide only.
    Fluorchemq Multiimage Iii Instrument, supplied by Alpha Innotech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/fluorchemq multiimage iii instrument/product/Alpha Innotech
    Average 90 stars, based on 1 article reviews
    fluorchemq multiimage iii instrument - by Bioz Stars, 2026-03
    90/100 stars
    		  Buy from Supplier
    multiimage iii instrument  (Alpha Innotech)
    90
    Alpha Innotech multiimage iii instrument
    Western blot validation of host protein regulation. A , HeLa cells were mock-infected or infected for 24 h, or B , for indicated periods of time, harvested and lysed with 0.5% NP-40 detergent. The cytosolic and nuclear fractions were separately purified, dissolved in SDS electrophoresis sample buffer, and proteins resolved in 10% ( A ), or in 4-16% gradient ( B ) SDS-PAGE, transferred to PVDF, and probed with indicated antibodies. Antibody binding was detected with HRP-conjugated secondary antibodies and ECL, and visualized with an Alpha Innotech <t>FluorChemQ</t> <t>MultiImage</t> <t>III</t> instrument. Molecular weight standards are indicated at left and SILAC-measured ratios are indicated on right in A . *: not detected in indicated fraction; †: based on single peptide only.
    Multiimage Iii Instrument, supplied by Alpha Innotech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/multiimage iii instrument/product/Alpha Innotech
    Average 90 stars, based on 1 article reviews
    multiimage iii instrument - by Bioz Stars, 2026-03
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    Western blot validation of host protein regulation. A , HeLa cells were mock-infected or infected for 24 h, or B , for indicated periods of time, harvested and lysed with 0.5% NP-40 detergent. The cytosolic and nuclear fractions were separately purified, dissolved in SDS electrophoresis sample buffer, and proteins resolved in 10% ( A ), or in 4-16% gradient ( B ) SDS-PAGE, transferred to PVDF, and probed with indicated antibodies. Antibody binding was detected with HRP-conjugated secondary antibodies and ECL, and visualized with an Alpha Innotech FluorChemQ MultiImage III instrument. Molecular weight standards are indicated at left and SILAC-measured ratios are indicated on right in A . *: not detected in indicated fraction; †: based on single peptide only.

    Journal: Virology Journal

    Article Title: HeLa cell response proteome alterations induced by mammalian reovirus T3D infection

    doi: 10.1186/1743-422X-10-202

    Figure Lengend Snippet: Western blot validation of host protein regulation. A , HeLa cells were mock-infected or infected for 24 h, or B , for indicated periods of time, harvested and lysed with 0.5% NP-40 detergent. The cytosolic and nuclear fractions were separately purified, dissolved in SDS electrophoresis sample buffer, and proteins resolved in 10% ( A ), or in 4-16% gradient ( B ) SDS-PAGE, transferred to PVDF, and probed with indicated antibodies. Antibody binding was detected with HRP-conjugated secondary antibodies and ECL, and visualized with an Alpha Innotech FluorChemQ MultiImage III instrument. Molecular weight standards are indicated at left and SILAC-measured ratios are indicated on right in A . *: not detected in indicated fraction; †: based on single peptide only.

    Article Snippet: Bands were developed by enhanced chemiluminescence and imaged with an Alpha Innotech FluorChemQ MultiImage III instrument.

    Techniques: Western Blot, Infection, Purification, Electrophoresis, SDS Page, Binding Assay, Molecular Weight