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gel filtration protein standards  (GE Healthcare)


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    Structured Review

    GE Healthcare gel filtration protein standards
    RAB37 promotes formation of the ATG12-ATG5-ATG16L1 complex in a GTP-dependent manner. a – c <t>Gel-filtration</t> analysis of the ATG12-ATG5-ATG16L1 complex by chromatography. Cell lysates of three cell lines (RAB37 overexpression, RAB37 knockdown and control HeLa cells) and two transiently transfected cells (FLAG-RAB37-Q89L and FLAG-RAB37-T43N) were separated by size-exclusion chromatography. Fractions were subjected to Western blotting with anti-ATG16L1 ( a ), anti-ATG5 ( b ) or anti-RAB37 antibody ( c ), respectively. The positions of the molecular mass <t>standards</t> in chromatography are showed in arrows. d Work model of RAB37 function together with ATG5-12 and ATG16L1 for autophagy
    Gel Filtration Protein Standards, supplied by GE Healthcare, used in various techniques. Bioz Stars score: 93/100, based on 465 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/gel filtration protein standards/product/GE Healthcare
    Average 93 stars, based on 465 article reviews
    gel filtration protein standards - by Bioz Stars, 2026-03
    93/100 stars

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    1) Product Images from "RAB37 interacts directly with ATG5 and promotes autophagosome formation via regulating ATG5-12-16 complex assembly"

    Article Title: RAB37 interacts directly with ATG5 and promotes autophagosome formation via regulating ATG5-12-16 complex assembly

    Journal: Cell Death and Differentiation

    doi: 10.1038/s41418-017-0023-1

    RAB37 promotes formation of the ATG12-ATG5-ATG16L1 complex in a GTP-dependent manner. a – c Gel-filtration analysis of the ATG12-ATG5-ATG16L1 complex by chromatography. Cell lysates of three cell lines (RAB37 overexpression, RAB37 knockdown and control HeLa cells) and two transiently transfected cells (FLAG-RAB37-Q89L and FLAG-RAB37-T43N) were separated by size-exclusion chromatography. Fractions were subjected to Western blotting with anti-ATG16L1 ( a ), anti-ATG5 ( b ) or anti-RAB37 antibody ( c ), respectively. The positions of the molecular mass standards in chromatography are showed in arrows. d Work model of RAB37 function together with ATG5-12 and ATG16L1 for autophagy
    Figure Legend Snippet: RAB37 promotes formation of the ATG12-ATG5-ATG16L1 complex in a GTP-dependent manner. a – c Gel-filtration analysis of the ATG12-ATG5-ATG16L1 complex by chromatography. Cell lysates of three cell lines (RAB37 overexpression, RAB37 knockdown and control HeLa cells) and two transiently transfected cells (FLAG-RAB37-Q89L and FLAG-RAB37-T43N) were separated by size-exclusion chromatography. Fractions were subjected to Western blotting with anti-ATG16L1 ( a ), anti-ATG5 ( b ) or anti-RAB37 antibody ( c ), respectively. The positions of the molecular mass standards in chromatography are showed in arrows. d Work model of RAB37 function together with ATG5-12 and ATG16L1 for autophagy

    Techniques Used: Filtration, Chromatography, Over Expression, Transfection, Size-exclusion Chromatography, Western Blot



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    RAB37 promotes formation of the ATG12-ATG5-ATG16L1 complex in a GTP-dependent manner. a – c <t>Gel-filtration</t> analysis of the ATG12-ATG5-ATG16L1 complex by chromatography. Cell lysates of three cell lines (RAB37 overexpression, RAB37 knockdown and control HeLa cells) and two transiently transfected cells (FLAG-RAB37-Q89L and FLAG-RAB37-T43N) were separated by size-exclusion chromatography. Fractions were subjected to Western blotting with anti-ATG16L1 ( a ), anti-ATG5 ( b ) or anti-RAB37 antibody ( c ), respectively. The positions of the molecular mass <t>standards</t> in chromatography are showed in arrows. d Work model of RAB37 function together with ATG5-12 and ATG16L1 for autophagy
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    RAB37 promotes formation of the ATG12-ATG5-ATG16L1 complex in a GTP-dependent manner. a – c Gel-filtration analysis of the ATG12-ATG5-ATG16L1 complex by chromatography. Cell lysates of three cell lines (RAB37 overexpression, RAB37 knockdown and control HeLa cells) and two transiently transfected cells (FLAG-RAB37-Q89L and FLAG-RAB37-T43N) were separated by size-exclusion chromatography. Fractions were subjected to Western blotting with anti-ATG16L1 ( a ), anti-ATG5 ( b ) or anti-RAB37 antibody ( c ), respectively. The positions of the molecular mass standards in chromatography are showed in arrows. d Work model of RAB37 function together with ATG5-12 and ATG16L1 for autophagy

    Journal: Cell Death and Differentiation

    Article Title: RAB37 interacts directly with ATG5 and promotes autophagosome formation via regulating ATG5-12-16 complex assembly

    doi: 10.1038/s41418-017-0023-1

    Figure Lengend Snippet: RAB37 promotes formation of the ATG12-ATG5-ATG16L1 complex in a GTP-dependent manner. a – c Gel-filtration analysis of the ATG12-ATG5-ATG16L1 complex by chromatography. Cell lysates of three cell lines (RAB37 overexpression, RAB37 knockdown and control HeLa cells) and two transiently transfected cells (FLAG-RAB37-Q89L and FLAG-RAB37-T43N) were separated by size-exclusion chromatography. Fractions were subjected to Western blotting with anti-ATG16L1 ( a ), anti-ATG5 ( b ) or anti-RAB37 antibody ( c ), respectively. The positions of the molecular mass standards in chromatography are showed in arrows. d Work model of RAB37 function together with ATG5-12 and ATG16L1 for autophagy

    Article Snippet: The column was calibrated with gel filtration protein standards (Cat# 28-4038-42, GE Healthcare Life Sciences, Fairfield, Connecticut, USA) containing thyroglobulin (669 kDa), ferritin (440 kDa), aldolase (158 kDa), Conalbumin (75 kDa), Ovalbumin (43 kDa).

    Techniques: Filtration, Chromatography, Over Expression, Transfection, Size-exclusion Chromatography, Western Blot