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APC-Cy7 Mouse Anti-Human IFN-γ Antibody (S-3076)

APC-Cy7 Mouse Anti-Human IFN-γ Antibody (S-3076)

Catalog Number: S0B80027 Application: ICFCM Reactivity: Human Conjugation: APC-Cy7 Brand: Starter
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Regular price $200 USD
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Product Details

Product Specification


Host Mouse
Antigen IFN-γ
Synonyms Interferon gamma; IFN-gamma; Immune interferon; IFNG
Location Secreted
Accession P01579
Clone Number S-3076
Antibody Type Mouse mAb
Isotype IgG1,k
Application ICFCM
Reactivity Hu
Positive Sample Th1 Polarization Human PBMC
Purification Protein G
Concentration 0.2 mg/ml
Conjugation APC-Cy7
Physical Appearance Liquid
Storage Buffer

PBS, 1% BSA, 0.3% Proclin 300

Stability & Storage

12 months from date of receipt / reconstitution, 2 to 8 °C as supplied

Dilution


application dilution species
ICFCM 1.25μl per million cells in 100μl volume Hu

Background

Interferon gamma (IFN-γ) is a dimerized soluble cytokine and the only member of the type II class of interferons. It is primarily produced by CD4+ T helper 1 (Th1) cells, natural killer (NK) cells, and CD8+ cytotoxic T cells. The IFN-γ protein is encoded by the IFNG gene in humans and consists of approximately 160 amino acids, forming a noncovalently linked homodimer with a molecular weight of about 50 kDa. It plays a crucial role in regulating both innate and adaptive immunity by activating signaling pathways, such as the JAK-STAT pathway, in cells like macrophages and B cells. IFN-γ has antiviral, antibacterial, and antitumor properties and is involved in promoting inflammation and cell proliferation. However, its pleiotropic nature also means it can induce immunosuppressive effects, which limit its clinical use.

Picture

FC

Flow cytometric analysis of IFN-γ expression in human PBMC polarized with Th1 Polarization Kit, Human (UA090016). Th1 polarized human PBMC were harvested and restimulated for 5 hr with PMA and Ionomycin in the presence of Brefeldin A.
The cells were harvested and fixed with 4% PFA and permeabilized with Intracellular Fixation & Permeabilization Buffer Set. The cells were then stained with PE Mouse Anti-Human CD4 and either APC-Cy7 Mouse IgG1, κ Isotype Control (left panel) or SDT APC-Cy7 Mouse Anti-Human IFN-γ Antibody (right panel) at 1.25μl/test treated with True-Stain Monocyte Blocker™. Total viable cells, as determined by Fixable Viability Dye 452 (S0D0021), were used for analysis. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.