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  • 91
    GE Healthcare superose 6 pc
    CTCF–Wrap53 RNA forms large-molecular-weight complexes. Purified CTCF, either FL ( A ) or the RBR ( B ) domain, was fractionated in a <t>Superose</t> 6 sizing column in the presence or absence of Wrap53 RNA.
    Superose 6 Pc, supplied by GE Healthcare, used in various techniques. Bioz Stars score: 91/100, based on 716 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    85
    GE Healthcare superose 6 pc 3 2 30
    CTCF–Wrap53 RNA forms large-molecular-weight complexes. Purified CTCF, either FL ( A ) or the RBR ( B ) domain, was fractionated in a <t>Superose</t> 6 sizing column in the presence or absence of Wrap53 RNA.
    Superose 6 Pc 3 2 30, supplied by GE Healthcare, used in various techniques. Bioz Stars score: 85/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    90
    GE Healthcare superose 6 pc column
    CTCF–Wrap53 RNA forms large-molecular-weight complexes. Purified CTCF, either FL ( A ) or the RBR ( B ) domain, was fractionated in a <t>Superose</t> 6 sizing column in the presence or absence of Wrap53 RNA.
    Superose 6 Pc Column, supplied by GE Healthcare, used in various techniques. Bioz Stars score: 90/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/superose 6 pc column/product/GE Healthcare
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    92
    GE Healthcare superose 6
    Analysis of myc 6 -Nup37 and myc 6 -Seh1 behavior by sucrose gradients. (A) Soluble extracts from HeLa cells (b and f) or from HeLa cells expressing myc 6 -Nup37 (a and d) or myc 6 -Seh1 (c and e) were loaded on continuous 20-35% sucrose gradients and centrifuged at 100,000 × g for 16 h. Fractions from the top (fraction 1) to the bottom (fraction 26) of the gradient were analyzed by Western blot by using anti-Nup133 (a), Nup85 (b), Nup37 (c), or myc (d and e) antibodies, or the mAb414 antibody (f). (B) Fractions 11-14 from the above-described sucrose gradient (b) were pooled, and 50 μl of the resulting sample was loaded on a <t>Superose</t> 6 (PC 3.2/30) gel filtration chromatography column. The initial sample (L) and the Superose 6 fractions were analyzed by Western blot by using anti-Nup133, Nup85, and Nup37 antibodies. Molecular size markers used to calibrate the sucrose gradient and the Superose 6 column are indicated. Thick bars denote the position of the Nup107-160 complex.
    Superose 6, supplied by GE Healthcare, used in various techniques. Bioz Stars score: 92/100, based on 1774 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/superose 6/product/GE Healthcare
    Average 92 stars, based on 1774 article reviews
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    Image Search Results


    CTCF–Wrap53 RNA forms large-molecular-weight complexes. Purified CTCF, either FL ( A ) or the RBR ( B ) domain, was fractionated in a Superose 6 sizing column in the presence or absence of Wrap53 RNA.

    Journal: Genes & Development

    Article Title: CTCF regulates the human p53 gene through direct interaction with its natural antisense transcript, Wrap53

    doi: 10.1101/gad.236869.113

    Figure Lengend Snippet: CTCF–Wrap53 RNA forms large-molecular-weight complexes. Purified CTCF, either FL ( A ) or the RBR ( B ) domain, was fractionated in a Superose 6 sizing column in the presence or absence of Wrap53 RNA.

    Article Snippet: Recombinant CTCF or RBRs were loaded onto a Superose 6 PC 3.2/30 (GE Life Sciences) 2.4-mL sizing column with or without Wrap53 RNA and fractionated.

    Techniques: Molecular Weight, Purification

    Analysis of myc 6 -Nup37 and myc 6 -Seh1 behavior by sucrose gradients. (A) Soluble extracts from HeLa cells (b and f) or from HeLa cells expressing myc 6 -Nup37 (a and d) or myc 6 -Seh1 (c and e) were loaded on continuous 20-35% sucrose gradients and centrifuged at 100,000 × g for 16 h. Fractions from the top (fraction 1) to the bottom (fraction 26) of the gradient were analyzed by Western blot by using anti-Nup133 (a), Nup85 (b), Nup37 (c), or myc (d and e) antibodies, or the mAb414 antibody (f). (B) Fractions 11-14 from the above-described sucrose gradient (b) were pooled, and 50 μl of the resulting sample was loaded on a Superose 6 (PC 3.2/30) gel filtration chromatography column. The initial sample (L) and the Superose 6 fractions were analyzed by Western blot by using anti-Nup133, Nup85, and Nup37 antibodies. Molecular size markers used to calibrate the sucrose gradient and the Superose 6 column are indicated. Thick bars denote the position of the Nup107-160 complex.

    Journal: Molecular Biology of the Cell

    Article Title: The Entire Nup107-160 Complex, Including Three New Members, Is Targeted as One Entity to Kinetochores in Mitosis D⃞

    doi: 10.1091/mbc.E03-12-0878

    Figure Lengend Snippet: Analysis of myc 6 -Nup37 and myc 6 -Seh1 behavior by sucrose gradients. (A) Soluble extracts from HeLa cells (b and f) or from HeLa cells expressing myc 6 -Nup37 (a and d) or myc 6 -Seh1 (c and e) were loaded on continuous 20-35% sucrose gradients and centrifuged at 100,000 × g for 16 h. Fractions from the top (fraction 1) to the bottom (fraction 26) of the gradient were analyzed by Western blot by using anti-Nup133 (a), Nup85 (b), Nup37 (c), or myc (d and e) antibodies, or the mAb414 antibody (f). (B) Fractions 11-14 from the above-described sucrose gradient (b) were pooled, and 50 μl of the resulting sample was loaded on a Superose 6 (PC 3.2/30) gel filtration chromatography column. The initial sample (L) and the Superose 6 fractions were analyzed by Western blot by using anti-Nup133, Nup85, and Nup37 antibodies. Molecular size markers used to calibrate the sucrose gradient and the Superose 6 column are indicated. Thick bars denote the position of the Nup107-160 complex.

    Article Snippet: Fractions 11-14 were pooled and 50 μl of the resulting sample were analyzed by gel filtration chromatography by using a Superose 6 (PC 3.2/30) column (Amersham Biosciences) equilibrated with lysis buffer (100 mM NaCl, 1 mM EDTA, 25 mM Tris, pH 7.5, 1% Triton X-100 reduced form).

    Techniques: Expressing, Western Blot, Filtration, Chromatography