rabbit anti ova igg (Worthington Biochemical)

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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:

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

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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

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

Techniques Used:

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: 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. ..