rabbit anti ova igg  (Worthington Biochemical)


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  • 91
    Name:
    Actin
    Description:
    Prepared by modification of the procedure of Spudich and Watt J Biol Chem 246 4866 1971 Purity checked by SDS PAGE A lyophilized powder
    Catalog Number:
    ls001041
    Price:
    46
    Size:
    1 mg
    Source:
    Rabbit Muscle
    Cas Number:
    51005.14.2
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    Structured Review

    Worthington Biochemical rabbit anti ova igg
    Mφ-II up-regulate SPHK1 and TNFSF14/LIGHT. (A) Relative SPHK1 mRNA as measured by real-time PCR after Mφ activation by LPS (●), LPS + <t>IgG-OVA</t> IC (▲), or IL-4 (○). (B) Relative LIGHT mRNA as measured by real-time PCR after Mφ activation by LPS (●), LPS + IgG-OVA IC (▲), or IL-4 (○). Calculation of fold values was detailed in Materials and Methods. (C) Immunoprecipitation of soluble LIGHT (sLIGHT) from 6 h cell supernatants of unstimulated Mφ, Ca-Mφ, and Mφ-II. Western blot analysis for LIGHT using a rat α-LIGHT mAb, showing the soluble form of LIGHT present as a 20- to 23-kD protein. Figures are representative of at least three independent experiments.
    Prepared by modification of the procedure of Spudich and Watt J Biol Chem 246 4866 1971 Purity checked by SDS PAGE A lyophilized powder
    https://www.bioz.com/result/rabbit anti ova igg/product/Worthington Biochemical
    Average 91 stars, based on 1823 article reviews
    Price from $9.99 to $1999.99
    rabbit anti ova igg - by Bioz Stars, 2021-01
    91/100 stars

    Images

    1) Product Images from "Biochemical and functional characterization of three activated macrophage populations"

    Article Title: Biochemical and functional characterization of three activated macrophage populations

    Journal: Journal of leukocyte biology

    doi: 10.1189/jlb.0406249

    Mφ-II up-regulate SPHK1 and TNFSF14/LIGHT. (A) Relative SPHK1 mRNA as measured by real-time PCR after Mφ activation by LPS (●), LPS + IgG-OVA IC (▲), or IL-4 (○). (B) Relative LIGHT mRNA as measured by real-time PCR after Mφ activation by LPS (●), LPS + IgG-OVA IC (▲), or IL-4 (○). Calculation of fold values was detailed in Materials and Methods. (C) Immunoprecipitation of soluble LIGHT (sLIGHT) from 6 h cell supernatants of unstimulated Mφ, Ca-Mφ, and Mφ-II. Western blot analysis for LIGHT using a rat α-LIGHT mAb, showing the soluble form of LIGHT present as a 20- to 23-kD protein. Figures are representative of at least three independent experiments.
    Figure Legend Snippet: Mφ-II up-regulate SPHK1 and TNFSF14/LIGHT. (A) Relative SPHK1 mRNA as measured by real-time PCR after Mφ activation by LPS (●), LPS + IgG-OVA IC (▲), or IL-4 (○). (B) Relative LIGHT mRNA as measured by real-time PCR after Mφ activation by LPS (●), LPS + IgG-OVA IC (▲), or IL-4 (○). Calculation of fold values was detailed in Materials and Methods. (C) Immunoprecipitation of soluble LIGHT (sLIGHT) from 6 h cell supernatants of unstimulated Mφ, Ca-Mφ, and Mφ-II. Western blot analysis for LIGHT using a rat α-LIGHT mAb, showing the soluble form of LIGHT present as a 20- to 23-kD protein. Figures are representative of at least three independent experiments.

    Techniques Used: Real-time Polymerase Chain Reaction, Activation Assay, Immunoprecipitation, Western Blot

    2) Product Images from "Bee venom phospholipase A2 induces a primary type 2 response that is dependent on the receptor ST2 and confers protective immunity"

    Article Title: Bee venom phospholipase A2 induces a primary type 2 response that is dependent on the receptor ST2 and confers protective immunity

    Journal: Immunity

    doi: 10.1016/j.immuni.2013.10.006

    PLA2 induces a Th2 response through cleavage of membrane phospholipids to produce lysophospholipids
    Figure Legend Snippet: PLA2 induces a Th2 response through cleavage of membrane phospholipids to produce lysophospholipids

    Techniques Used:

    Related Articles

    Incubation:

    Article Title: In Situ Natural Product Discovery via an Artificial Marine Sponge
    Article Snippet: .. Reverse–Affinity Purification An aliquot of an Affigel 10 resin (2 mL) bearing 2.2±0.8 mg/mL of rabbit muscle actin (Worthington Biochemical) was incubated with 520 mg of the SES–009 extract in 5 mL of 50 mM phosphate buffered saline (PBS) buffer pH 8.0 containing 0.2 mM CaCl2 and 5% DMSO. .. After shaking by inversion for 12 h at 4°C, the resin was collected via centrifugation on a C–1200 mini–centrifuge (VWR Scientific) for 2 min.

    Activity Assay:

    Article Title: Different virulence of candida albicans is attributed to the ability of escape from neutrophil extracellular traps by secretion of DNase
    Article Snippet: .. Neutrophils with C. albicans were designed as seven groups: a group with exogenous DNase (100 U/ml) (Sigma, USA); a group with 100 μg/ml G-actin (Worthington, USA) to inhibit DNase activity; a group with exogenous DNase and 10 μg/ml cytochalasin D (sigma, USA) to inhibit both phagocytotic uptake and extracellular killing; a group with exogenous catalase (100 U/ml) (Worthington, USA); a group with 3-Amino-1,2,4-triazole (AT) (1 mM) (Calbiochem, Germany) to inhibit catalase activity; a group with exogenous catalase and cytochalasin D; and a group without neutrophils as an internal control to determine baseline fungal counts. .. DNase activity assays were conducted by using exogenous DNA and agarose gel electrophoresis as described by Buchanan et al. [ ].

    Labeling:

    Article Title: Marinopyrrole A Target Elucidation by Acyl Dye Transfer
    Article Snippet: .. Samples of rabbit muscle actin (Worthington Biochemicals) were treated with 13 or 14 to yield comparable fluorescently labeled bands (lanes L4-L7, ). ..

    Purification:

    Article Title: In Situ Natural Product Discovery via an Artificial Marine Sponge
    Article Snippet: .. Reverse–Affinity Purification An aliquot of an Affigel 10 resin (2 mL) bearing 2.2±0.8 mg/mL of rabbit muscle actin (Worthington Biochemical) was incubated with 520 mg of the SES–009 extract in 5 mL of 50 mM phosphate buffered saline (PBS) buffer pH 8.0 containing 0.2 mM CaCl2 and 5% DMSO. .. After shaking by inversion for 12 h at 4°C, the resin was collected via centrifugation on a C–1200 mini–centrifuge (VWR Scientific) for 2 min.

    Article Title: Characterization of the Enzymatic Component of Clostridium perfringens Iota-Toxin
    Article Snippet: .. Purified rabbit muscle actin was purchased from Worthington Biochemical Corp., Lakewood, N.J. All other chemicals were of analytical grade. ..

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    Worthington Biochemical nierenberg aa
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