macro prep highq Search Results


macro prep high q column  (Bio-Rad)
95
Bio-Rad macro prep high q column
Macro Prep High Q Column, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/macro+prep+highq/Macro-Prep+High+Q+Support/pmc05878146-75-8-12
Average 95 stars, based on 1 article reviews
macro prep high q column - by Bioz Stars, 2026-09
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macro prep high s  (Bio-Rad)
94
Bio-Rad macro prep high s
Macro Prep High S, 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/macro+prep+highq/Macro-Prep+High+S+Support/pmc07112681-107-6-13
Average 94 stars, based on 1 article reviews
macro prep high s - by Bioz Stars, 2026-09
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deae cellulose  (Bio-Rad)
94
Bio-Rad deae cellulose
Design of a hybrid protein (hMIKO‐1) and its purification. (a) The frames of the full‐length AA sequences of hS100A8 and hS100A9 were schematically drawn by blue and gray horizontal bars, respectively. hMIKO‐1 is a hybrid protein of hS100A8 and hS100A9. The whole frame of hMIKO‐1 was as follows: 21 AA residues from the C terminus of hS100A9 were added to the C terminus of hS100A8. (b) SDS–PAGE (15% gel) was performed to confirm the purity of hMIKO‐1 in the absence of 2‐mercaptoethanol. hMIKO‐1 was purified by affinity chromatography (Ni‐agarose; Nacalai Tesque, Kyoto, Japan), ion‐exchange chromatography <t>(DEAE</t> cellulose; Bio‐Rad Co., Ltd, USA) and gel filtration (Sephacryl S‐300 HR). Proteins in the gel were stained with Coomassie Brilliant Blue. Lanes M and 1 were molecular markers and purified hMIKO‐1, respectively. As shown in the kit (Toxinsensor, Endotoxin Detection System; GenScript Inc., USA), the concentration <t>of</t> <t>contaminated</t> endotoxin present in the product hMIKO‐1 was less than 0.3 EU mg −1 protein. This result indicates no significant effects in subsequent experiments (data not shown). AA, amino acid; PAGE, polyacrylamide gel electrophoresis; SDS, sodium dodecyl sulfate.
Deae Cellulose, 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/macro+prep+highq/Macro-Prep+DEAE+Support/pmc11964790-26-10-16
Average 94 stars, based on 1 article reviews
deae cellulose - by Bioz Stars, 2026-09
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macroprep high s  (Bio-Rad)
91
Bio-Rad macroprep high s
Design of a hybrid protein (hMIKO‐1) and its purification. (a) The frames of the full‐length AA sequences of hS100A8 and hS100A9 were schematically drawn by blue and gray horizontal bars, respectively. hMIKO‐1 is a hybrid protein of hS100A8 and hS100A9. The whole frame of hMIKO‐1 was as follows: 21 AA residues from the C terminus of hS100A9 were added to the C terminus of hS100A8. (b) SDS–PAGE (15% gel) was performed to confirm the purity of hMIKO‐1 in the absence of 2‐mercaptoethanol. hMIKO‐1 was purified by affinity chromatography (Ni‐agarose; Nacalai Tesque, Kyoto, Japan), ion‐exchange chromatography <t>(DEAE</t> cellulose; Bio‐Rad Co., Ltd, USA) and gel filtration (Sephacryl S‐300 HR). Proteins in the gel were stained with Coomassie Brilliant Blue. Lanes M and 1 were molecular markers and purified hMIKO‐1, respectively. As shown in the kit (Toxinsensor, Endotoxin Detection System; GenScript Inc., USA), the concentration <t>of</t> <t>contaminated</t> endotoxin present in the product hMIKO‐1 was less than 0.3 EU mg −1 protein. This result indicates no significant effects in subsequent experiments (data not shown). AA, amino acid; PAGE, polyacrylamide gel electrophoresis; SDS, sodium dodecyl sulfate.
Macroprep High S, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/macro+prep+highq/Bio-Scale+Mini+Macro-Prep+High+S+Cartridges/10__1074_slash_jbc__m412263200-153-13-16
Average 91 stars, based on 1 article reviews
macroprep high s - by Bioz Stars, 2026-09
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cation exchange chromatography  (Bio-Rad)
94
Bio-Rad cation exchange chromatography
Design of a hybrid protein (hMIKO‐1) and its purification. (a) The frames of the full‐length AA sequences of hS100A8 and hS100A9 were schematically drawn by blue and gray horizontal bars, respectively. hMIKO‐1 is a hybrid protein of hS100A8 and hS100A9. The whole frame of hMIKO‐1 was as follows: 21 AA residues from the C terminus of hS100A9 were added to the C terminus of hS100A8. (b) SDS–PAGE (15% gel) was performed to confirm the purity of hMIKO‐1 in the absence of 2‐mercaptoethanol. hMIKO‐1 was purified by affinity chromatography (Ni‐agarose; Nacalai Tesque, Kyoto, Japan), ion‐exchange chromatography <t>(DEAE</t> cellulose; Bio‐Rad Co., Ltd, USA) and gel filtration (Sephacryl S‐300 HR). Proteins in the gel were stained with Coomassie Brilliant Blue. Lanes M and 1 were molecular markers and purified hMIKO‐1, respectively. As shown in the kit (Toxinsensor, Endotoxin Detection System; GenScript Inc., USA), the concentration <t>of</t> <t>contaminated</t> endotoxin present in the product hMIKO‐1 was less than 0.3 EU mg −1 protein. This result indicates no significant effects in subsequent experiments (data not shown). AA, amino acid; PAGE, polyacrylamide gel electrophoresis; SDS, sodium dodecyl sulfate.
Cation Exchange Chromatography, 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/macro+prep+highq/Protein+Standard+for+Cation+Exchange+Chromatography/pm34308939-66-9-17
Average 94 stars, based on 1 article reviews
cation exchange chromatography - by Bioz Stars, 2026-09
94/100 stars
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cation exchange column macro prep high s  (Bio-Rad)
93
Bio-Rad cation exchange column macro prep high s
Design of a hybrid protein (hMIKO‐1) and its purification. (a) The frames of the full‐length AA sequences of hS100A8 and hS100A9 were schematically drawn by blue and gray horizontal bars, respectively. hMIKO‐1 is a hybrid protein of hS100A8 and hS100A9. The whole frame of hMIKO‐1 was as follows: 21 AA residues from the C terminus of hS100A9 were added to the C terminus of hS100A8. (b) SDS–PAGE (15% gel) was performed to confirm the purity of hMIKO‐1 in the absence of 2‐mercaptoethanol. hMIKO‐1 was purified by affinity chromatography (Ni‐agarose; Nacalai Tesque, Kyoto, Japan), ion‐exchange chromatography <t>(DEAE</t> cellulose; Bio‐Rad Co., Ltd, USA) and gel filtration (Sephacryl S‐300 HR). Proteins in the gel were stained with Coomassie Brilliant Blue. Lanes M and 1 were molecular markers and purified hMIKO‐1, respectively. As shown in the kit (Toxinsensor, Endotoxin Detection System; GenScript Inc., USA), the concentration <t>of</t> <t>contaminated</t> endotoxin present in the product hMIKO‐1 was less than 0.3 EU mg −1 protein. This result indicates no significant effects in subsequent experiments (data not shown). AA, amino acid; PAGE, polyacrylamide gel electrophoresis; SDS, sodium dodecyl sulfate.
Cation Exchange Column Macro Prep High S, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/macro+prep+highq/EconoFit+Macro-Prep+High+S+Columns/bio_rxiv__2025__04__21__649818-246-12-18
Average 93 stars, based on 1 article reviews
cation exchange column macro prep high s - by Bioz Stars, 2026-09
93/100 stars
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methyl 3h sam usingmacro prep highq resin  (Bio-Rad)
93
Bio-Rad methyl 3h sam usingmacro prep highq resin
Design of a hybrid protein (hMIKO‐1) and its purification. (a) The frames of the full‐length AA sequences of hS100A8 and hS100A9 were schematically drawn by blue and gray horizontal bars, respectively. hMIKO‐1 is a hybrid protein of hS100A8 and hS100A9. The whole frame of hMIKO‐1 was as follows: 21 AA residues from the C terminus of hS100A9 were added to the C terminus of hS100A8. (b) SDS–PAGE (15% gel) was performed to confirm the purity of hMIKO‐1 in the absence of 2‐mercaptoethanol. hMIKO‐1 was purified by affinity chromatography (Ni‐agarose; Nacalai Tesque, Kyoto, Japan), ion‐exchange chromatography <t>(DEAE</t> cellulose; Bio‐Rad Co., Ltd, USA) and gel filtration (Sephacryl S‐300 HR). Proteins in the gel were stained with Coomassie Brilliant Blue. Lanes M and 1 were molecular markers and purified hMIKO‐1, respectively. As shown in the kit (Toxinsensor, Endotoxin Detection System; GenScript Inc., USA), the concentration <t>of</t> <t>contaminated</t> endotoxin present in the product hMIKO‐1 was less than 0.3 EU mg −1 protein. This result indicates no significant effects in subsequent experiments (data not shown). AA, amino acid; PAGE, polyacrylamide gel electrophoresis; SDS, sodium dodecyl sulfate.
Methyl 3h Sam Usingmacro Prep Highq Resin, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/macro+prep+highq/Macro-Prep+Methyl+HIC+Support/10__1074_slash_jbc__m112__410290-147-6-10
Average 93 stars, based on 1 article reviews
methyl 3h sam usingmacro prep highq resin - by Bioz Stars, 2026-09
93/100 stars
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anion exchange chromatography  (Bio-Rad)
93
Bio-Rad anion exchange chromatography
Design of a hybrid protein (hMIKO‐1) and its purification. (a) The frames of the full‐length AA sequences of hS100A8 and hS100A9 were schematically drawn by blue and gray horizontal bars, respectively. hMIKO‐1 is a hybrid protein of hS100A8 and hS100A9. The whole frame of hMIKO‐1 was as follows: 21 AA residues from the C terminus of hS100A9 were added to the C terminus of hS100A8. (b) SDS–PAGE (15% gel) was performed to confirm the purity of hMIKO‐1 in the absence of 2‐mercaptoethanol. hMIKO‐1 was purified by affinity chromatography (Ni‐agarose; Nacalai Tesque, Kyoto, Japan), ion‐exchange chromatography <t>(DEAE</t> cellulose; Bio‐Rad Co., Ltd, USA) and gel filtration (Sephacryl S‐300 HR). Proteins in the gel were stained with Coomassie Brilliant Blue. Lanes M and 1 were molecular markers and purified hMIKO‐1, respectively. As shown in the kit (Toxinsensor, Endotoxin Detection System; GenScript Inc., USA), the concentration <t>of</t> <t>contaminated</t> endotoxin present in the product hMIKO‐1 was less than 0.3 EU mg −1 protein. This result indicates no significant effects in subsequent experiments (data not shown). AA, amino acid; PAGE, polyacrylamide gel electrophoresis; SDS, sodium dodecyl sulfate.
Anion Exchange Chromatography, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/macro+prep+highq/Bio-Scale+Mini+Macro-Prep+High+Q+Cartridge/pmc03177201-87-4-7
Average 93 stars, based on 1 article reviews
anion exchange chromatography - by Bioz Stars, 2026-09
93/100 stars
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macroprep high s column  (Bio-Rad)
93
Bio-Rad macroprep high s column
Design of a hybrid protein (hMIKO‐1) and its purification. (a) The frames of the full‐length AA sequences of hS100A8 and hS100A9 were schematically drawn by blue and gray horizontal bars, respectively. hMIKO‐1 is a hybrid protein of hS100A8 and hS100A9. The whole frame of hMIKO‐1 was as follows: 21 AA residues from the C terminus of hS100A9 were added to the C terminus of hS100A8. (b) SDS–PAGE (15% gel) was performed to confirm the purity of hMIKO‐1 in the absence of 2‐mercaptoethanol. hMIKO‐1 was purified by affinity chromatography (Ni‐agarose; Nacalai Tesque, Kyoto, Japan), ion‐exchange chromatography <t>(DEAE</t> cellulose; Bio‐Rad Co., Ltd, USA) and gel filtration (Sephacryl S‐300 HR). Proteins in the gel were stained with Coomassie Brilliant Blue. Lanes M and 1 were molecular markers and purified hMIKO‐1, respectively. As shown in the kit (Toxinsensor, Endotoxin Detection System; GenScript Inc., USA), the concentration <t>of</t> <t>contaminated</t> endotoxin present in the product hMIKO‐1 was less than 0.3 EU mg −1 protein. This result indicates no significant effects in subsequent experiments (data not shown). AA, amino acid; PAGE, polyacrylamide gel electrophoresis; SDS, sodium dodecyl sulfate.
Macroprep High S Column, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/macro+prep+highq/EconoFit+Macro-Prep+High+S+Column/pm21307596-43-12-19
Average 93 stars, based on 1 article reviews
macroprep high s column - by Bioz Stars, 2026-09
93/100 stars
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anion exchanger macro prep high 25 q  (Bio-Rad)
93
Bio-Rad anion exchanger macro prep high 25 q
Design of a hybrid protein (hMIKO‐1) and its purification. (a) The frames of the full‐length AA sequences of hS100A8 and hS100A9 were schematically drawn by blue and gray horizontal bars, respectively. hMIKO‐1 is a hybrid protein of hS100A8 and hS100A9. The whole frame of hMIKO‐1 was as follows: 21 AA residues from the C terminus of hS100A9 were added to the C terminus of hS100A8. (b) SDS–PAGE (15% gel) was performed to confirm the purity of hMIKO‐1 in the absence of 2‐mercaptoethanol. hMIKO‐1 was purified by affinity chromatography (Ni‐agarose; Nacalai Tesque, Kyoto, Japan), ion‐exchange chromatography <t>(DEAE</t> cellulose; Bio‐Rad Co., Ltd, USA) and gel filtration (Sephacryl S‐300 HR). Proteins in the gel were stained with Coomassie Brilliant Blue. Lanes M and 1 were molecular markers and purified hMIKO‐1, respectively. As shown in the kit (Toxinsensor, Endotoxin Detection System; GenScript Inc., USA), the concentration <t>of</t> <t>contaminated</t> endotoxin present in the product hMIKO‐1 was less than 0.3 EU mg −1 protein. This result indicates no significant effects in subsequent experiments (data not shown). AA, amino acid; PAGE, polyacrylamide gel electrophoresis; SDS, sodium dodecyl sulfate.
Anion Exchanger Macro Prep High 25 Q, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/macro+prep+highq/Macro-Prep+25+Q+Support/pmc03722206-110-23-30
Average 93 stars, based on 1 article reviews
anion exchanger macro prep high 25 q - by Bioz Stars, 2026-09
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macro prep high q support  (Bio-Rad)
98
Bio-Rad macro prep high q support
Design of a hybrid protein (hMIKO‐1) and its purification. (a) The frames of the full‐length AA sequences of hS100A8 and hS100A9 were schematically drawn by blue and gray horizontal bars, respectively. hMIKO‐1 is a hybrid protein of hS100A8 and hS100A9. The whole frame of hMIKO‐1 was as follows: 21 AA residues from the C terminus of hS100A9 were added to the C terminus of hS100A8. (b) SDS–PAGE (15% gel) was performed to confirm the purity of hMIKO‐1 in the absence of 2‐mercaptoethanol. hMIKO‐1 was purified by affinity chromatography (Ni‐agarose; Nacalai Tesque, Kyoto, Japan), ion‐exchange chromatography <t>(DEAE</t> cellulose; Bio‐Rad Co., Ltd, USA) and gel filtration (Sephacryl S‐300 HR). Proteins in the gel were stained with Coomassie Brilliant Blue. Lanes M and 1 were molecular markers and purified hMIKO‐1, respectively. As shown in the kit (Toxinsensor, Endotoxin Detection System; GenScript Inc., USA), the concentration <t>of</t> <t>contaminated</t> endotoxin present in the product hMIKO‐1 was less than 0.3 EU mg −1 protein. This result indicates no significant effects in subsequent experiments (data not shown). AA, amino acid; PAGE, polyacrylamide gel electrophoresis; SDS, sodium dodecyl sulfate.
Macro Prep High Q Support, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/macro+prep+highq/Tris/pmc00114128-171-3-7
Average 98 stars, based on 1 article reviews
macro prep high q support - by Bioz Stars, 2026-09
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Image Search Results


Design of a hybrid protein (hMIKO‐1) and its purification. (a) The frames of the full‐length AA sequences of hS100A8 and hS100A9 were schematically drawn by blue and gray horizontal bars, respectively. hMIKO‐1 is a hybrid protein of hS100A8 and hS100A9. The whole frame of hMIKO‐1 was as follows: 21 AA residues from the C terminus of hS100A9 were added to the C terminus of hS100A8. (b) SDS–PAGE (15% gel) was performed to confirm the purity of hMIKO‐1 in the absence of 2‐mercaptoethanol. hMIKO‐1 was purified by affinity chromatography (Ni‐agarose; Nacalai Tesque, Kyoto, Japan), ion‐exchange chromatography (DEAE cellulose; Bio‐Rad Co., Ltd, USA) and gel filtration (Sephacryl S‐300 HR). Proteins in the gel were stained with Coomassie Brilliant Blue. Lanes M and 1 were molecular markers and purified hMIKO‐1, respectively. As shown in the kit (Toxinsensor, Endotoxin Detection System; GenScript Inc., USA), the concentration of contaminated endotoxin present in the product hMIKO‐1 was less than 0.3 EU mg −1 protein. This result indicates no significant effects in subsequent experiments (data not shown). AA, amino acid; PAGE, polyacrylamide gel electrophoresis; SDS, sodium dodecyl sulfate.

Journal: Immunology and Cell Biology

Article Title: A hybrid protein is a functional molecule to reduce the cytokine storm caused by excessively activated macrophages

doi: 10.1111/imcb.70000

Figure Lengend Snippet: Design of a hybrid protein (hMIKO‐1) and its purification. (a) The frames of the full‐length AA sequences of hS100A8 and hS100A9 were schematically drawn by blue and gray horizontal bars, respectively. hMIKO‐1 is a hybrid protein of hS100A8 and hS100A9. The whole frame of hMIKO‐1 was as follows: 21 AA residues from the C terminus of hS100A9 were added to the C terminus of hS100A8. (b) SDS–PAGE (15% gel) was performed to confirm the purity of hMIKO‐1 in the absence of 2‐mercaptoethanol. hMIKO‐1 was purified by affinity chromatography (Ni‐agarose; Nacalai Tesque, Kyoto, Japan), ion‐exchange chromatography (DEAE cellulose; Bio‐Rad Co., Ltd, USA) and gel filtration (Sephacryl S‐300 HR). Proteins in the gel were stained with Coomassie Brilliant Blue. Lanes M and 1 were molecular markers and purified hMIKO‐1, respectively. As shown in the kit (Toxinsensor, Endotoxin Detection System; GenScript Inc., USA), the concentration of contaminated endotoxin present in the product hMIKO‐1 was less than 0.3 EU mg −1 protein. This result indicates no significant effects in subsequent experiments (data not shown). AA, amino acid; PAGE, polyacrylamide gel electrophoresis; SDS, sodium dodecyl sulfate.

Article Snippet: Contaminated endotoxin was deleted as much as possible using a DEAE cellulose (Macro‐Prep High Q Media, Bio‐Rad, USA) column [26 mm (D) × 80 mm (L)].

Techniques: Purification, SDS Page, Affinity Chromatography, Ion Exchange Chromatography, Filtration, Staining, Concentration Assay, Polyacrylamide Gel Electrophoresis