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prestained molecular weight markers (bio‐rad)  (Bio-Rad)


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    Bio-Rad prestained molecular weight markers (bio‐rad)
    Prestained Molecular Weight Markers (Bio‐Rad), supplied by Bio-Rad, 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/result/prestained molecular weight markers (bio‐rad)/product/Bio-Rad
    Average 90 stars, based on 1 article reviews
    prestained molecular weight markers (bio‐rad) - by Bioz Stars, 2026-03
    90/100 stars

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    Fig. 2. Western blot analysis of mock- and channel catfish virus (CCV)-infected brown bullhead (BB) cell lysates using catfish serum. Cell lysates and supernatants were separated by 12% SDS-PAGE and blotted onto nitrocellulose mem- branes. (A) Positive control catfish serum against mock- infected cell lysates (L1) and supernatants (S1) or aganist CCV-infected cell lysates (L2) and supernatants (S2). Markers are Bio-Rad <t>Prestained</t> SDS-PAGE broad range molecular weight markers <t>(M1)</t> and Amersham ECL protein molecular weight markers (M2). (B) The humoral immune profile at 0, 30, 60, and 90 d post challenge, and 10 d post treatment (PT) with dexamethasone (DEX, 0.55 mg kg–1 body weight) from 2 CCV/DEX-treated fish (lanes 1 to 5 and 6 to 10) representing positive samples and from 1 mock/DEX-treated fish (lanes 11 to 15) representing a negative sample in western blots. Posi- tive (+) and negative (–) fish serum controls; M = ECL protein molecular weight markers (Amersham). No bands were detected with these samples in blots on mock-infected BB cell lysates (patterns were identical to negative fish serum control)
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    Fig. 2. Western blot analysis of mock- and channel catfish virus (CCV)-infected brown bullhead (BB) cell lysates using catfish serum. Cell lysates and supernatants were separated by 12% SDS-PAGE and blotted onto nitrocellulose mem- branes. (A) Positive control catfish serum against mock- infected cell lysates (L1) and supernatants (S1) or aganist CCV-infected cell lysates (L2) and supernatants (S2). Markers are Bio-Rad <t>Prestained</t> SDS-PAGE broad range molecular weight markers <t>(M1)</t> and Amersham ECL protein molecular weight markers (M2). (B) The humoral immune profile at 0, 30, 60, and 90 d post challenge, and 10 d post treatment (PT) with dexamethasone (DEX, 0.55 mg kg–1 body weight) from 2 CCV/DEX-treated fish (lanes 1 to 5 and 6 to 10) representing positive samples and from 1 mock/DEX-treated fish (lanes 11 to 15) representing a negative sample in western blots. Posi- tive (+) and negative (–) fish serum controls; M = ECL protein molecular weight markers (Amersham). No bands were detected with these samples in blots on mock-infected BB cell lysates (patterns were identical to negative fish serum control)
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    Fig. 2. Western blot analysis of mock- and channel catfish virus (CCV)-infected brown bullhead (BB) cell lysates using catfish serum. Cell lysates and supernatants were separated by 12% SDS-PAGE and blotted onto nitrocellulose mem- branes. (A) Positive control catfish serum against mock- infected cell lysates (L1) and supernatants (S1) or aganist CCV-infected cell lysates (L2) and supernatants (S2). Markers are Bio-Rad <t>Prestained</t> SDS-PAGE broad range molecular weight markers <t>(M1)</t> and Amersham ECL protein molecular weight markers (M2). (B) The humoral immune profile at 0, 30, 60, and 90 d post challenge, and 10 d post treatment (PT) with dexamethasone (DEX, 0.55 mg kg–1 body weight) from 2 CCV/DEX-treated fish (lanes 1 to 5 and 6 to 10) representing positive samples and from 1 mock/DEX-treated fish (lanes 11 to 15) representing a negative sample in western blots. Posi- tive (+) and negative (–) fish serum controls; M = ECL protein molecular weight markers (Amersham). No bands were detected with these samples in blots on mock-infected BB cell lysates (patterns were identical to negative fish serum control)
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    Fig. 2. Western blot analysis of mock- and channel catfish virus (CCV)-infected brown bullhead (BB) cell lysates using catfish serum. Cell lysates and supernatants were separated by 12% SDS-PAGE and blotted onto nitrocellulose mem- branes. (A) Positive control catfish serum against mock- infected cell lysates (L1) and supernatants (S1) or aganist CCV-infected cell lysates (L2) and supernatants (S2). Markers are Bio-Rad <t>Prestained</t> SDS-PAGE broad range molecular weight markers <t>(M1)</t> and Amersham ECL protein molecular weight markers (M2). (B) The humoral immune profile at 0, 30, 60, and 90 d post challenge, and 10 d post treatment (PT) with dexamethasone (DEX, 0.55 mg kg–1 body weight) from 2 CCV/DEX-treated fish (lanes 1 to 5 and 6 to 10) representing positive samples and from 1 mock/DEX-treated fish (lanes 11 to 15) representing a negative sample in western blots. Posi- tive (+) and negative (–) fish serum controls; M = ECL protein molecular weight markers (Amersham). No bands were detected with these samples in blots on mock-infected BB cell lysates (patterns were identical to negative fish serum control)
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    Fig. 2. Western blot analysis of mock- and channel catfish virus (CCV)-infected brown bullhead (BB) cell lysates using catfish serum. Cell lysates and supernatants were separated by 12% SDS-PAGE and blotted onto nitrocellulose mem- branes. (A) Positive control catfish serum against mock- infected cell lysates (L1) and supernatants (S1) or aganist CCV-infected cell lysates (L2) and supernatants (S2). Markers are Bio-Rad <t>Prestained</t> SDS-PAGE broad range molecular weight markers <t>(M1)</t> and Amersham ECL protein molecular weight markers (M2). (B) The humoral immune profile at 0, 30, 60, and 90 d post challenge, and 10 d post treatment (PT) with dexamethasone (DEX, 0.55 mg kg–1 body weight) from 2 CCV/DEX-treated fish (lanes 1 to 5 and 6 to 10) representing positive samples and from 1 mock/DEX-treated fish (lanes 11 to 15) representing a negative sample in western blots. Posi- tive (+) and negative (–) fish serum controls; M = ECL protein molecular weight markers (Amersham). No bands were detected with these samples in blots on mock-infected BB cell lysates (patterns were identical to negative fish serum control)
    Prestained Molecular Weight Markers (Bio–Rad), supplied by Bio-Rad, 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/result/prestained molecular weight markers (bio–rad)/product/Bio-Rad
    Average 90 stars, based on 1 article reviews
    prestained molecular weight markers (bio–rad) - by Bioz Stars, 2026-03
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    Fig. 2. Western blot analysis of mock- and channel catfish virus (CCV)-infected brown bullhead (BB) cell lysates using catfish serum. Cell lysates and supernatants were separated by 12% SDS-PAGE and blotted onto nitrocellulose mem- branes. (A) Positive control catfish serum against mock- infected cell lysates (L1) and supernatants (S1) or aganist CCV-infected cell lysates (L2) and supernatants (S2). Markers are Bio-Rad Prestained SDS-PAGE broad range molecular weight markers (M1) and Amersham ECL protein molecular weight markers (M2). (B) The humoral immune profile at 0, 30, 60, and 90 d post challenge, and 10 d post treatment (PT) with dexamethasone (DEX, 0.55 mg kg–1 body weight) from 2 CCV/DEX-treated fish (lanes 1 to 5 and 6 to 10) representing positive samples and from 1 mock/DEX-treated fish (lanes 11 to 15) representing a negative sample in western blots. Posi- tive (+) and negative (–) fish serum controls; M = ECL protein molecular weight markers (Amersham). No bands were detected with these samples in blots on mock-infected BB cell lysates (patterns were identical to negative fish serum control)

    Journal: Diseases of aquatic organisms

    Article Title: Antibody response of channel catfish after channel catfish virus infection and following dexamethasone treatment.

    doi: 10.3354/dao02348

    Figure Lengend Snippet: Fig. 2. Western blot analysis of mock- and channel catfish virus (CCV)-infected brown bullhead (BB) cell lysates using catfish serum. Cell lysates and supernatants were separated by 12% SDS-PAGE and blotted onto nitrocellulose mem- branes. (A) Positive control catfish serum against mock- infected cell lysates (L1) and supernatants (S1) or aganist CCV-infected cell lysates (L2) and supernatants (S2). Markers are Bio-Rad Prestained SDS-PAGE broad range molecular weight markers (M1) and Amersham ECL protein molecular weight markers (M2). (B) The humoral immune profile at 0, 30, 60, and 90 d post challenge, and 10 d post treatment (PT) with dexamethasone (DEX, 0.55 mg kg–1 body weight) from 2 CCV/DEX-treated fish (lanes 1 to 5 and 6 to 10) representing positive samples and from 1 mock/DEX-treated fish (lanes 11 to 15) representing a negative sample in western blots. Posi- tive (+) and negative (–) fish serum controls; M = ECL protein molecular weight markers (Amersham). No bands were detected with these samples in blots on mock-infected BB cell lysates (patterns were identical to negative fish serum control)

    Article Snippet: Markers are Bio-Rad Prestained SDS-PAGE broad range molecular weight markers (M1) and Amersham ECL protein molecular weight markers (M2). (B) The humoral immune profile at 0, 30, 60, and 90 d post challenge, and 10 d post treatment (PT) with dexamethasone (DEX, 0.55 mg kg–1 body weight) from 2 CCV/DEX-treated fish (lanes 1 to 5 and 6 to 10) representing positive samples and from 1 mock/DEX-treated fish (lanes 11 to 15) representing a negative sample in western blots.

    Techniques: Western Blot, Virus, Infection, SDS Page, Positive Control, Molecular Weight, Control