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H l igg

Manufactured by Thermo Fisher Scientific
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Sourced in United States

The H + L IgG is a laboratory equipment product designed to detect the presence of immunoglobulin G (IgG) antibodies in biological samples. It functions as a detection reagent, providing a reliable method to identify IgG levels.

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Lab products found in correlation

Alexa fluor 488, by Thermo Fisher Scientific (6 mentions) Alexa fluor 568, by Thermo Fisher Scientific (6 mentions)

Close spelling variants of this product

Alexa Fluor 647 goat anti-rabbit IgG (H+L) antibody Alexa Fluor ™ 647-conjugated goat anti-human IgG (H + L) antibody Alexa fluor 488 conjugated anti-mouse IgG (H+L) Alexa Fluor 488 goat anti-mouse immunoglobulin G (IgG) (H+L) Cross-adsorbed goat anti-human IgG (H+L) secondary antibody Goat anti-rabbit IgG (H+L) conjugated with Alexa Fluor 488 Alexa Fluor 594 donkey anti-mouse IgG (H+L) Alexa fluor 555 conjugated donkey anti-rabbit IgG (H+L) Alexa Fluor® 488 conjugated Donkey Anti-Rabbit IgG (H + L) antibody Alexa Fluor 647-conjugated F(ab′)2-Goat anti-mouse IgG (H+L) secondary antibody

3 protocols using h l igg

1

Immunostaining Detection Protocols

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Detection of immunostaining was carried out using horseradish peroxidase–diaminobenzidine (see above) for immunohistochemistry and secondary antibodies conjugated with Alexa Fluor® 488 (1:1000, donkey anti-rabbit, H + L IgG, Thermo Fischer Scientific, Waltham, ME, USA) and Alexa Fluor® 568 (1:1000, donkey anti-mouse, H + L IgG, Thermo Fischer Scientific, Waltham, ME, USA) for immunofluorescence staining. Slides incubated with only the secondary antibody were used as specificity controls.
Jankovska N., Rusina R., Keller J., Kukal J., Bruzova M., Parobkova E., Olejar T, & Matej R. (2022). Biomarkers Analysis and Clinical Manifestations in Comorbid Creutzfeldt–Jakob Disease: A Retrospective Study in 215 Autopsy Cases. Biomedicines, 10(3), 680.
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2

Immunohistochemical and Immunofluorescence Staining

Check if the same lab product or an alternative is used in the 5 most similar protocols
Detection of immunostaining was carried out using horseradish peroxidase–diaminobenzidine (see above) for immunohistochemistry and secondary antibodies conjugated with Alexa Fluor® 488 (1:1000, donkey anti-rabbit, H + L IgG, Thermo Fischer Scientific, Waltham, MA, USA) and Alexa Fluor® 568 (1:1000, donkey anti-mouse, H + L IgG, Thermo Fischer Scientific, Waltham, MA, USA) for immunofluorescence staining. Slides incubated with only the secondary antibody were used as specificity controls.
Jankovska N., Matej R, & Olejar T. (2021). Extracellular Prion Protein Aggregates in Nine Gerstmann–Sträussler–Scheinker Syndrome Subjects with Mutation P102L: A Micromorphological Study and Comparison with Literature Data. International Journal of Molecular Sciences, 22(24), 13303.
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3

Immunostaining Detection Protocols

Check if the same lab product or an alternative is used in the 5 most similar protocols
Detection of immunostaining was carried out using horseradish peroxidase–diaminobenzidine (see above) for immunohistochemistry and secondary antibodies conjugated with Alexa Fluor® 488 (1:1000, donkey anti-rabbit, H + L IgG, Thermo Fischer Scientific, Waltham, MA, USA) and Alexa Fluor® 568 (1:1000, donkey anti-mouse, H + L IgG, Thermo Fischer Scientific) for immunofluorescence staining. Slides incubated with only the secondary antibody were used as specificity controls.
Jankovska N., Olejar T, & Matej R. (2021). Extracellular Protein Aggregates Colocalization and Neuronal Dystrophy in Comorbid Alzheimer’s and Creutzfeldt–Jakob Disease: A Micromorphological Pilot Study on 20 Brains. International Journal of Molecular Sciences, 22(4), 2099.
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