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Glycoprotein stain

Manufactured by Thermo Fisher Scientific
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Glycoprotein stain is a laboratory reagent used to detect and visualize glycoproteins in electrophoretic gels or western blots. It binds to the carbohydrate moieties of glycoproteins, allowing their identification and quantification.

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Lab products found in correlation

Endoglycosidase h, by New England Biolabs (2 mentions) α2 3 6 8 9 neuraminidase a, by New England Biolabs (2 mentions) Pngase f, by New England Biolabs (2 mentions)

Close spelling variants of this product

Pro-Q Emerald 300 Glycoprotein gel stain kit ProQ Emerald glycoprotein stain Pro‐Q® Emerald 300 Glycoprotein Gel and Blot Stain Kit Pro-Q Emerald glycoprotein gel and blot stain kit

2 protocols using glycoprotein stain

1

Deglycosylation of Nanoparticle Immunogens

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Nanoparticle immunogens were deglycosylated using PNGase F (New England BioLabs P0704S), endoglycosidase H (New England BioLabs P0702S), or α2–3,6,8,9 neuraminidase A (New England BioLabs P0722S) under non-denaturing conditions following the manufacturer’s guidelines. Deglycosylation was confirmed via SDS-PAGE gel using glycoprotein stain (ThermoFisher 24562). Retention of particle structure was confirmed via dynamic light scattering.
Read B.J., Won L., Kraft J.C., Sappington I., Aung A., Wu S., Bals J., Chen C., Lee K.K., Lingwood D., King N.P, & Irvine D.J. (2022). Mannose-binding lectin and complement mediate follicular localization and enhanced immunogenicity of diverse protein nanoparticle immunogens. Cell reports, 38(2), 110217.
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2

Deglycosylation of Nanoparticle Immunogens

Check if the same lab product or an alternative is used in the 5 most similar protocols
Nanoparticle immunogens were deglycosylated using PNGase F (New England BioLabs P0704S), endoglycosidase H (New England BioLabs P0702S), or α2–3,6,8,9 neuraminidase A (New England BioLabs P0722S) under non-denaturing conditions following the manufacturer’s guidelines. Deglycosylation was confirmed via SDS-PAGE gel using glycoprotein stain (ThermoFisher 24562). Retention of particle structure was confirmed via dynamic light scattering.
Read B.J., Won L., Kraft J.C., Sappington I., Aung A., Wu S., Bals J., Chen C., Lee K.K., Lingwood D., King N.P, & Irvine D.J. (2022). Mannose-binding lectin and complement mediate follicular localization and enhanced immunogenicity of diverse protein nanoparticle immunogens. Cell reports, 38(2), 110217.
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