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sepharose column  (Danaher Inc)


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    Structured Review

    Danaher Inc sepharose column
    Sepharose Column, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 93/100, based on 77 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/weak+cation+exchanger+array/HiTrap+CM+FF/pmc05063504-73-10-15
    Average 93 stars, based on 77 article reviews
    sepharose column - by Bioz Stars, 2026-11
    93/100 stars

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    Related Articles

    Centrifugation:

    Article Title: Arabidopsis AtPME2 has a pH-dependent processivity and control cell wall mechanical properties
    Article Snippet: .. Culture supernatants recovered following centrifugation, were applied onto a CM-FF Hi trap cation-exchange column following the manufacturer’s instructions (GE-Healthcare). ..

    Western Blot:

    Article Title: Bacterial-type ferroxidase tunes iron-dependent phosphate sensing during Arabidopsis root development
    Article Snippet: The resulting protein pellet was solubilized in 2-3 ml buffer A, loaded on a HighLoad Superdex 200 gel filtration column (HL 16/60, GE Healthcare), and eluted with buffer A as the mobile phase. .. Fractions containing LPR1 (detected by immunoblot analysis) were directly applied to cation exchange carboxymethyl-sepharose column (HiTrap CM FF, 1-ml, GE Healthcare) equilibrated with buffer B (20 mM Na 2 HPO 4 -NaH 2 PO 4 , pH 7). ..

    Recombinant:

    Article Title: Molecular and functional characterization of an evolutionarily conserved CREB-binding protein in the Lymnaea CNS.
    Article Snippet: Expression of the partial recombinant protein of the LymCBP catalytic domain was induced by treatment with 0.32 mM of isopropyl β- d- thiogalactopyranoside (IPTG) in TBG- M9 medium [0.8% Bacto Tryptone (BD) and 0.4% NaCl], followed by purification using nickel- nitrilotriacetic acid (Ni- NTA) agarose resin (QIAGEN). .. The recombinant protein was desalted with a PD- 10 column (SephadexTM G- 25 M, GE Healthcare), purified using a cation exchange column [HiTrap carboxymethyl (CM) FF column (GE Healthcare)] installed in the ÄKTAprime plus system (GE Healthcare), and condensed with Amicon® Ultra- 15 column (Merck Millipore). .. The procedures followed to perform this experiment were modified from previous reports.36- 40 The recombinant LymCBP HAT domain (200 ng) was incubated with histone H1 purified from calf thymus (1 μg, SigmaAldrich) and 7.4 kBq of [14C]- acetyl- CoA (Moravek, Inc.) for 4 h in buffer containing 50 mM Tris– HCl (pH 8.0), 10% glycerol, 1 mM dithiothreitol, and 10 mM sodium butyrate.

    Article Title: Histone acetyltransferase activity of CREB-binding protein is essential for synaptic plasticity in Lymnaea
    Article Snippet: Expression of the partial recombinant protein of the LymCBP catalytic domain was induced by treatment with 0.32 mM of isopropyl β-D-thiogalactopyranoside (IPTG) in TBG-M9 medium [0.8% Bacto Tryptone (BD) and 0.4% NaCl], followed by purification using nickel-nitrilotriacetic acid (Ni-NTA) agarose resin (QIAGEN). .. The recombinant protein was desalted with PD-10 column (Sephadex TM G-25M, GE Healthcare), purified using a cation exchange column [HiTrap carboxymethyl (CM) FF column (GE Healthcare)] installed in the ÄKTAprime plus system (GE Healthcare), and condensed with Amicon ® Ultra-15 column (Merck Millipore). ..

    Purification:

    Article Title: Molecular and functional characterization of an evolutionarily conserved CREB-binding protein in the Lymnaea CNS.
    Article Snippet: Expression of the partial recombinant protein of the LymCBP catalytic domain was induced by treatment with 0.32 mM of isopropyl β- d- thiogalactopyranoside (IPTG) in TBG- M9 medium [0.8% Bacto Tryptone (BD) and 0.4% NaCl], followed by purification using nickel- nitrilotriacetic acid (Ni- NTA) agarose resin (QIAGEN). .. The recombinant protein was desalted with a PD- 10 column (SephadexTM G- 25 M, GE Healthcare), purified using a cation exchange column [HiTrap carboxymethyl (CM) FF column (GE Healthcare)] installed in the ÄKTAprime plus system (GE Healthcare), and condensed with Amicon® Ultra- 15 column (Merck Millipore). .. The procedures followed to perform this experiment were modified from previous reports.36- 40 The recombinant LymCBP HAT domain (200 ng) was incubated with histone H1 purified from calf thymus (1 μg, SigmaAldrich) and 7.4 kBq of [14C]- acetyl- CoA (Moravek, Inc.) for 4 h in buffer containing 50 mM Tris– HCl (pH 8.0), 10% glycerol, 1 mM dithiothreitol, and 10 mM sodium butyrate.

    Article Title: Histone acetyltransferase activity of CREB-binding protein is essential for synaptic plasticity in Lymnaea
    Article Snippet: Expression of the partial recombinant protein of the LymCBP catalytic domain was induced by treatment with 0.32 mM of isopropyl β-D-thiogalactopyranoside (IPTG) in TBG-M9 medium [0.8% Bacto Tryptone (BD) and 0.4% NaCl], followed by purification using nickel-nitrilotriacetic acid (Ni-NTA) agarose resin (QIAGEN). .. The recombinant protein was desalted with PD-10 column (Sephadex TM G-25M, GE Healthcare), purified using a cation exchange column [HiTrap carboxymethyl (CM) FF column (GE Healthcare)] installed in the ÄKTAprime plus system (GE Healthcare), and condensed with Amicon ® Ultra-15 column (Merck Millipore). ..

    other:

    Article Title: Structures of an engineered phospholipase D with specificity for secondary alcohol transphosphatidylation: insights into plasticity of substrate binding and activation
    Article Snippet: Four consecutive chromatography steps were used in the purification process: (1) anion exchange chromatography (5 ml HiTrap Q FF column, GE Healthcare; gradient elution with NaCl in 20 mM Tris–HCl pH 8.0 buffer), (2) affinity chromatography (5 ml Maltose-Binding-Protein/MBPTrap HP column, GE Healthcare; isocratic elution with 150 mM NaCl in 20 mM Tris–HCl pH 8.0 buffer), (3) cation exchange chromatography (1 ml HiTrap CM FF column, GE Healthcare; gradient elution with NaCl in 50 mM acetate buffer pH 5.0) and (4) size exclusion chromatography (HiLoad Superdex75 16/60 column, GE Healthcare; isocratic elution with 150 mM NaCl in 20 mM Tris–HCl pH 8.0 buffer).



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    L-OHP sensitivity and candidate peak selection . (A) Protein expression profiles of each cell line on <t>CM10</t> array at pH 4.5. The candidate peak is enclosed by the rectangle. (B) Peak intensity of the 11.1 kDa protein in 11 CRC cell lines strongly correlates with L-OHP sensitivity. The peak intensity and IC 50 value of each cell line are plotted as means ± S.D. (peak intensity, n = 3; IC 50 , n = 3 or 4).
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    Image Search Results


    L-OHP sensitivity and candidate peak selection . (A) Protein expression profiles of each cell line on CM10 array at pH 4.5. The candidate peak is enclosed by the rectangle. (B) Peak intensity of the 11.1 kDa protein in 11 CRC cell lines strongly correlates with L-OHP sensitivity. The peak intensity and IC 50 value of each cell line are plotted as means ± S.D. (peak intensity, n = 3; IC 50 , n = 3 or 4).

    Journal: Proteome Science

    Article Title: S100A10 protein expression is associated with oxaliplatin sensitivity in human colorectal cancer cells

    doi: 10.1186/1477-5956-9-76

    Figure Lengend Snippet: L-OHP sensitivity and candidate peak selection . (A) Protein expression profiles of each cell line on CM10 array at pH 4.5. The candidate peak is enclosed by the rectangle. (B) Peak intensity of the 11.1 kDa protein in 11 CRC cell lines strongly correlates with L-OHP sensitivity. The peak intensity and IC 50 value of each cell line are plotted as means ± S.D. (peak intensity, n = 3; IC 50 , n = 3 or 4).

    Article Snippet: Weak cation-exchange ProteinChip CM10 arrays (Bio-Rad Laboratories, Hercules, CA, USA) were used for protein profiling.

    Techniques: Selection, Expressing

    Characterization of the 11.1 kDa protein . (A) Estimation of pI of the 11.1 kDa protein. The affinity of the 11.1 kDa protein (indicated by the arrow) to a CM10 array changed with a pH range of 3.0-10.0. (B) Estimation of experimental molecular mass of the 11.1 kDa protein (indicated by the arrow). Bovine insulin (5733.5 Da) and equine cytochrome C (12361.0 Da) were calibrants for internal calibration.

    Journal: Proteome Science

    Article Title: S100A10 protein expression is associated with oxaliplatin sensitivity in human colorectal cancer cells

    doi: 10.1186/1477-5956-9-76

    Figure Lengend Snippet: Characterization of the 11.1 kDa protein . (A) Estimation of pI of the 11.1 kDa protein. The affinity of the 11.1 kDa protein (indicated by the arrow) to a CM10 array changed with a pH range of 3.0-10.0. (B) Estimation of experimental molecular mass of the 11.1 kDa protein (indicated by the arrow). Bovine insulin (5733.5 Da) and equine cytochrome C (12361.0 Da) were calibrants for internal calibration.

    Article Snippet: Weak cation-exchange ProteinChip CM10 arrays (Bio-Rad Laboratories, Hercules, CA, USA) were used for protein profiling.

    Techniques: