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anti rabbit immunoglobulin g  (Bio-Rad)


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    Structured Review

    Bio-Rad anti rabbit immunoglobulin g
    Anti Rabbit Immunoglobulin G, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 45 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+salmonid+ig+antibody/Rabbit+anti+Salmonid+Ig/pm40846737-198-10-28
    Average 93 stars, based on 45 article reviews
    anti rabbit immunoglobulin g - by Bioz Stars, 2026-09
    93/100 stars

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    Related Articles

    Enzyme-linked Immunosorbent Assay:

    Article Title: Kinetics of Parasite-Specific Antibody and B-Cell-Associated Gene Expression in Brown Trout, Salmo trutta during Proliferative Kidney Disease
    Article Snippet: .. The optimisation of the ELISA was accomplished with T. bryosalmonae antigen ranging from 1.0 to 10.0 μg/mL, serum dilutions from 1:20–1:800, rabbit anti-salmonid Ig antibody (Bio-Rad, product code: AHP761) dilutions from 1:1500–1:9000, and peroxidase-conjugated antirabbit IgG (whole molecule) antibody (Sigma-Aldrich) dilutions from 1:1500–1:12,000. .. A 96-well microtiter plate (MaxiSorp TM , Nunc, TherrmoFisher Scientific, Roskilde, Denmark) was coated with 100 μL/well parasite antigen (2.0 μg/mL) in bicarbonate coating buffer (pH 9.6, Sigma-Aldrich) and incubated overnight at 4 °C.

    Incubation:

    Article Title: Delayed sexual maturation through gonadotropin receptor vaccination in the rainbow trout Oncorhynchus mykiss.
    Article Snippet: In fish, gonadotropin hormones FSH-GTH1 and LH-GTH2 are less specific for their cognate receptors than in mammals.. The respective reproductive functions of fish LH and FSH are thus difficult to establish.. We aimed to study the effect of specific antagonists of the two gonadotropin receptors on trout sexual maturation in both sexes by targeting specific regions of LH and FSH receptors, Lhr and Fshr.



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    Image Search Results


    Antibodies used (listed in alphabetical order) for Western blotting (WB) and (or) immunogold labeling (IGL).

    Journal: Biomolecules

    Article Title: The Passage of Chaperonins to Extracellular Locations in Legionella pneumophila Requires a Functional Dot/Icm System

    doi: 10.3390/biom15010091

    Figure Lengend Snippet: Antibodies used (listed in alphabetical order) for Western blotting (WB) and (or) immunogold labeling (IGL).

    Article Snippet: αMouseAP , Commercial rabbit purified immunoglobulin G conjugated to alkaline phosphatase. Diluted 1:5000 for WB , Cedarlane Labs 5.

    Techniques: Western Blot, Labeling, Recombinant, Cell Culture, Purification

    Immunoblots of SDS-PAGE-resolved proteins from whole bacterial cells treated with trypsin (250 µg trypsin/10 9 bacteria), and immunostained with an HtpB-specific monoclonal antibody and alkaline phosphatase-conjugated rabbit anti-mouse IgG. ( A ) Band patterns produced in the wild-type strain Lp02 and its dotA − derivative JV309. Trypsin-accessible HtpB is evidenced by the immunolabeled degradation products of <60 kDa. The presence of trypsin-accessible HtpB was recovered in the trans -complemented dotA − mutant ( dotA − + C). ( B , C ) Band patterns showing the lack of trypsin-accessible HtpB in two different dotB mutants: dotB − (with a loss-of-function point mutation), and Δ dotB (with a deletion of the dotB gene). A recovery of trypsin-accessible HtpB was observed in trans -complemented dotB mutants ( dotB + C and Δ dotB + C), but not in the mock-complemented mutants carrying an empty vector ( dotB + V and Δ dotB + V). Abbreviations for all panels: “C” = control, trypsin-free sample, “T” = trypsin-treated sample. Arrows at the far left indicate the position of three of the broad-range pre-stained protein size markers (New England Biolabs, Whitby, ON, Canada) corresponding to (from top to bottom) 62, 47 and 37.5 kDa.

    Journal: Biomolecules

    Article Title: The Passage of Chaperonins to Extracellular Locations in Legionella pneumophila Requires a Functional Dot/Icm System

    doi: 10.3390/biom15010091

    Figure Lengend Snippet: Immunoblots of SDS-PAGE-resolved proteins from whole bacterial cells treated with trypsin (250 µg trypsin/10 9 bacteria), and immunostained with an HtpB-specific monoclonal antibody and alkaline phosphatase-conjugated rabbit anti-mouse IgG. ( A ) Band patterns produced in the wild-type strain Lp02 and its dotA − derivative JV309. Trypsin-accessible HtpB is evidenced by the immunolabeled degradation products of <60 kDa. The presence of trypsin-accessible HtpB was recovered in the trans -complemented dotA − mutant ( dotA − + C). ( B , C ) Band patterns showing the lack of trypsin-accessible HtpB in two different dotB mutants: dotB − (with a loss-of-function point mutation), and Δ dotB (with a deletion of the dotB gene). A recovery of trypsin-accessible HtpB was observed in trans -complemented dotB mutants ( dotB + C and Δ dotB + C), but not in the mock-complemented mutants carrying an empty vector ( dotB + V and Δ dotB + V). Abbreviations for all panels: “C” = control, trypsin-free sample, “T” = trypsin-treated sample. Arrows at the far left indicate the position of three of the broad-range pre-stained protein size markers (New England Biolabs, Whitby, ON, Canada) corresponding to (from top to bottom) 62, 47 and 37.5 kDa.

    Article Snippet: αMouseAP , Commercial rabbit purified immunoglobulin G conjugated to alkaline phosphatase. Diluted 1:5000 for WB , Cedarlane Labs 5.

    Techniques: Western Blot, SDS Page, Bacteria, Produced, Immunolabeling, Mutagenesis, Plasmid Preparation, Control, Staining