coomassie brilliant blue r Search Results


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Gold Biotechnology Inc coomassie brilliant blue r 250
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Bio-Rad bio safe coomassie brilliant blue staining solution
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Bio-Rad coomassie brilliant blue r 250
Coomassie Brilliant Blue R 250, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Valiant Co Ltd coomassie brilliant blue r250 staining
Coomassie Brilliant Blue R250 Staining, supplied by Valiant Co Ltd, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bio-Rad destain solutions
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Bio-Rad destaining buffer
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Fluka Chemical coomassie brilliant blue r-250
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EM Science Inc coomassie brilliant blue r-250
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Amresco coomassie blue
Approximately 1 µg of each mAb was separated under reduced (A) and non-reduced (B) conditions. Both gels were stained with <t>Coomassie</t> Blue dye. The heavy (HC) and light (LC) chains of the following antibodies are shown: 1) αDEC, 2) αDCIR2, 3) αDEC-NS1, 4) αDCIR2-NS1. (C) Western blotting using anti-mouse IgG and anti-mouse kappa chain conjugated to HRP to verify the recognition of both heavy and light chains of each antibody. The numbers indicate the same order as in (A). (D) Western blotting on a non-reduced gel using a mouse serum raised against the dimeric form of NS1 followed by protein A conjugated to HRP. Columns 1–4, same as (A), column 5 contains 1 µg of NS1 produced in bacteria (Di_NS1: dimeric NS1 and Mo_NS1: monomeric NS1). Specific reaction was obtained only in columns containing NS1. MW, molecular weight marker in kDa.
Coomassie Blue, supplied by Amresco, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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FUJIFILM coomassie brilliant blue r-250 (cbb
Approximately 1 µg of each mAb was separated under reduced (A) and non-reduced (B) conditions. Both gels were stained with <t>Coomassie</t> Blue dye. The heavy (HC) and light (LC) chains of the following antibodies are shown: 1) αDEC, 2) αDCIR2, 3) αDEC-NS1, 4) αDCIR2-NS1. (C) Western blotting using anti-mouse IgG and anti-mouse kappa chain conjugated to HRP to verify the recognition of both heavy and light chains of each antibody. The numbers indicate the same order as in (A). (D) Western blotting on a non-reduced gel using a mouse serum raised against the dimeric form of NS1 followed by protein A conjugated to HRP. Columns 1–4, same as (A), column 5 contains 1 µg of NS1 produced in bacteria (Di_NS1: dimeric NS1 and Mo_NS1: monomeric NS1). Specific reaction was obtained only in columns containing NS1. MW, molecular weight marker in kDa.
Coomassie Brilliant Blue R 250 (Cbb, supplied by FUJIFILM, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Merck KGaA coomassie brilliant blue r-250 staining
Approximately 1 µg of each mAb was separated under reduced (A) and non-reduced (B) conditions. Both gels were stained with <t>Coomassie</t> Blue dye. The heavy (HC) and light (LC) chains of the following antibodies are shown: 1) αDEC, 2) αDCIR2, 3) αDEC-NS1, 4) αDCIR2-NS1. (C) Western blotting using anti-mouse IgG and anti-mouse kappa chain conjugated to HRP to verify the recognition of both heavy and light chains of each antibody. The numbers indicate the same order as in (A). (D) Western blotting on a non-reduced gel using a mouse serum raised against the dimeric form of NS1 followed by protein A conjugated to HRP. Columns 1–4, same as (A), column 5 contains 1 µg of NS1 produced in bacteria (Di_NS1: dimeric NS1 and Mo_NS1: monomeric NS1). Specific reaction was obtained only in columns containing NS1. MW, molecular weight marker in kDa.
Coomassie Brilliant Blue R 250 Staining, supplied by Merck KGaA, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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BioShop coomassie briliant blue g-250
Approximately 1 µg of each mAb was separated under reduced (A) and non-reduced (B) conditions. Both gels were stained with <t>Coomassie</t> Blue dye. The heavy (HC) and light (LC) chains of the following antibodies are shown: 1) αDEC, 2) αDCIR2, 3) αDEC-NS1, 4) αDCIR2-NS1. (C) Western blotting using anti-mouse IgG and anti-mouse kappa chain conjugated to HRP to verify the recognition of both heavy and light chains of each antibody. The numbers indicate the same order as in (A). (D) Western blotting on a non-reduced gel using a mouse serum raised against the dimeric form of NS1 followed by protein A conjugated to HRP. Columns 1–4, same as (A), column 5 contains 1 µg of NS1 produced in bacteria (Di_NS1: dimeric NS1 and Mo_NS1: monomeric NS1). Specific reaction was obtained only in columns containing NS1. MW, molecular weight marker in kDa.
Coomassie Briliant Blue G 250, supplied by BioShop, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Approximately 1 µg of each mAb was separated under reduced (A) and non-reduced (B) conditions. Both gels were stained with Coomassie Blue dye. The heavy (HC) and light (LC) chains of the following antibodies are shown: 1) αDEC, 2) αDCIR2, 3) αDEC-NS1, 4) αDCIR2-NS1. (C) Western blotting using anti-mouse IgG and anti-mouse kappa chain conjugated to HRP to verify the recognition of both heavy and light chains of each antibody. The numbers indicate the same order as in (A). (D) Western blotting on a non-reduced gel using a mouse serum raised against the dimeric form of NS1 followed by protein A conjugated to HRP. Columns 1–4, same as (A), column 5 contains 1 µg of NS1 produced in bacteria (Di_NS1: dimeric NS1 and Mo_NS1: monomeric NS1). Specific reaction was obtained only in columns containing NS1. MW, molecular weight marker in kDa.

Journal: PLoS Neglected Tropical Diseases

Article Title: Targeting the Non-structural Protein 1 from Dengue Virus to a Dendritic Cell Population Confers Protective Immunity to Lethal Virus Challenge

doi: 10.1371/journal.pntd.0002330

Figure Lengend Snippet: Approximately 1 µg of each mAb was separated under reduced (A) and non-reduced (B) conditions. Both gels were stained with Coomassie Blue dye. The heavy (HC) and light (LC) chains of the following antibodies are shown: 1) αDEC, 2) αDCIR2, 3) αDEC-NS1, 4) αDCIR2-NS1. (C) Western blotting using anti-mouse IgG and anti-mouse kappa chain conjugated to HRP to verify the recognition of both heavy and light chains of each antibody. The numbers indicate the same order as in (A). (D) Western blotting on a non-reduced gel using a mouse serum raised against the dimeric form of NS1 followed by protein A conjugated to HRP. Columns 1–4, same as (A), column 5 contains 1 µg of NS1 produced in bacteria (Di_NS1: dimeric NS1 and Mo_NS1: monomeric NS1). Specific reaction was obtained only in columns containing NS1. MW, molecular weight marker in kDa.

Article Snippet: Gels were either stained with Coomassie Blue (Amresco) or transferred to nitrocellulose membranes (GE Healthcare).

Techniques: Staining, Western Blot, Produced, Molecular Weight, Marker