sypro ruby protein gel staining Search Results


sypro ruby protein gel stain  (Thermo Fisher)
N/A
SYPRO® Ruby Protein Gel Stain is a highly sensitive, ready-to-use fluorescent stain for the detection of proteins separated by polyacrylamide gel electrophoresis (PAGE). SYPRO® Ruby stain is ideal for use in 1D and 2D PAGE.
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sypro ruby protein gel stain  (Bio-Rad)
94
Bio-Rad sypro ruby protein gel stain
Fig. 8 SDS-PAGE and Western blot analysis of proteins isolated from giant basal spicules after HF treatment (M size marker). a Extracts were separated by SDS-PAGE (10% polyacrylamide/0.1% SDS). Untreated (lane a) and deglycosylated (lane b) preparations were size- separated. After separation on the gels, the polypeptides were visualized with <t>Sypro</t> <t>Ruby</t> protein gel stain. b Western blot analysis of proteins in the extracts from spicules not treated with glycosidases. The proteins were subjected to SDS-PAGE (12% polyacrylamide/ 0.1% SDS) and electrophoresed. After blot transfer, the proteins were reacted with anti-silicatein polyclonal antibodies. Immunocomplexes (arrowhead) were visualized with an alkaline-phosphatase-labeled secondary antibody (lane a)
Sypro Ruby Protein Gel Stain, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sypro+ruby+protein+gel+staining/SYPRO+Ruby+Protein+Gel+Stain/pm17406901-61-21-27
Average 94 stars, based on 1 article reviews
sypro ruby protein gel stain - by Bioz Stars, 2026-09
94/100 stars
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sypro ruby protein gel stain (cat. no. s1200)  (Promega)
90
Promega sypro ruby protein gel stain (cat. no. s1200)
Fig. 8 SDS-PAGE and Western blot analysis of proteins isolated from giant basal spicules after HF treatment (M size marker). a Extracts were separated by SDS-PAGE (10% polyacrylamide/0.1% SDS). Untreated (lane a) and deglycosylated (lane b) preparations were size- separated. After separation on the gels, the polypeptides were visualized with <t>Sypro</t> <t>Ruby</t> protein gel stain. b Western blot analysis of proteins in the extracts from spicules not treated with glycosidases. The proteins were subjected to SDS-PAGE (12% polyacrylamide/ 0.1% SDS) and electrophoresed. After blot transfer, the proteins were reacted with anti-silicatein polyclonal antibodies. Immunocomplexes (arrowhead) were visualized with an alkaline-phosphatase-labeled secondary antibody (lane a)
Sypro Ruby Protein Gel Stain (Cat. No. S1200), supplied by Promega, 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/product/sypro+ruby+protein+gel+staining/Sypro+Ruby+Protein+Gel+Stain++Cat++No++S1200/pm28442447-60-5-16
Average 90 stars, based on 1 article reviews
sypro ruby protein gel stain (cat. no. s1200) - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier
dodeca stainer and sypro ruby protein gel stain  (Bio-Rad)
N/A
100–240 V, large gel staining device (#165-3400) and SYPRO staining solution for a large tank, sufficient for up to 12 large format gels
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sypro ruby protein gel stain  (Lonza)
N/A
SYPRO® Ruby Gel Stain, 200 mL
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Fig. 8 SDS-PAGE and Western blot analysis of proteins isolated from giant basal spicules after HF treatment (M size marker). a Extracts were separated by SDS-PAGE (10% polyacrylamide/0.1% SDS). Untreated (lane a) and deglycosylated (lane b) preparations were size- separated. After separation on the gels, the polypeptides were visualized with Sypro Ruby protein gel stain. b Western blot analysis of proteins in the extracts from spicules not treated with glycosidases. The proteins were subjected to SDS-PAGE (12% polyacrylamide/ 0.1% SDS) and electrophoresed. After blot transfer, the proteins were reacted with anti-silicatein polyclonal antibodies. Immunocomplexes (arrowhead) were visualized with an alkaline-phosphatase-labeled secondary antibody (lane a)

Journal: Cell and tissue research

Article Title: Formation of giant spicules in the deep-sea hexactinellid Monorhaphis chuni (Schulze 1904): electron-microscopic and biochemical studies.

doi: 10.1007/s00441-007-0402-x

Figure Lengend Snippet: Fig. 8 SDS-PAGE and Western blot analysis of proteins isolated from giant basal spicules after HF treatment (M size marker). a Extracts were separated by SDS-PAGE (10% polyacrylamide/0.1% SDS). Untreated (lane a) and deglycosylated (lane b) preparations were size- separated. After separation on the gels, the polypeptides were visualized with Sypro Ruby protein gel stain. b Western blot analysis of proteins in the extracts from spicules not treated with glycosidases. The proteins were subjected to SDS-PAGE (12% polyacrylamide/ 0.1% SDS) and electrophoresed. After blot transfer, the proteins were reacted with anti-silicatein polyclonal antibodies. Immunocomplexes (arrowhead) were visualized with an alkaline-phosphatase-labeled secondary antibody (lane a)

Article Snippet: Materials Enzymatic CarboRelease kit (No. KEDG-01) was obtained from QA-Bio (Novatec, Basel, Switzerland); electrophoresis loading buffer (RothiLoad4) from Roth (Karlsruhe, Germany); Sypro Ruby protein gel stain from BioRad (München, Germany); casein and Coomassie Brilliant Blue from Serva (Heidelberg, Germany); Sirius Red [3BA], tetraethoxysilane (TEOS), and Rhodamine 123 from SigmaAldrich (Taufkirchen, Germany); horse blood from Fiebig Nährstofftechnik (Germany); and GelCode blue from Perbio (Bonn, Germany).

Techniques: SDS Page, Western Blot, Isolation, Marker, Staining, Labeling