MBL

Anti-IFN-gamma (Human) mAb

Product Code:
 
MBL-D112-3
Product Group:
 
Primary Antibodies
Supplier:
 
MBL
Host Type:
 
Mouse
Antibody Isotype:
 
IgG1
Antibody Clonality:
 
Monoclonal
Antibody Clone:
 
6
Regulatory Status:
 
RUO
Target Species:
 
Human
Application:
 
Neutralisation
Shipping:
 
4°C
Storage:
 
-20°C
 

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MBL-D112-3100 ug£296.00
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  • Further Information
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Further Information

Applications:
NT - 3.95x103 (NU/mL) The apparent neutralizing effect of antibody against IFN-γ may vary depending on cell types and growth conditions. The amounts of neutralized IFN-γ activity by the serially diluted antibodies were measured under the condition stated in the following APPLICATION. The diluted antibody at the dilution factor 3.95 x 103 may neutralize the 1 IU/mL (International Reference Unit) of IFN-γ in the solution, that is, 1 NU/mL (arbitrary standardized neutralizing unit) of antibody may neutralize the 1 IU/mL of IFN-γ activity in the solution.
Background:
IFN-γ, also known as type II interferon, is mainly produced in activated T lymphocytes and NK cells. It is involved in the regulation of nearly all phases of immune and inflammatory responses, such as the activation, growth, and differentiation of T cells, B cells, macrophages and also several other cell types, including endothelial cells and fibroblasts. IFN-γ has antiviral and antiproliferative activities, it has also been shown to inhibit the proliferation of a variety of cells. Synthesis of IFN-γ is upregulated by IL2, FGF basic and EGF.
Concentration:
1 mg/mL
Formulation:
100 ug IgG in 100 ul volume of PBS containing 50% glycerol, pH 7.2. No preservative iscontained.
Gene IDs:
Human: 3458 Mouse: 15978
Immunogen Translated:
Purified human IFN-γ
Reactivity:
This antibody neutralizes human IFN-γ
Shelf Life:
1 year
Source:
This antibody was purified from hybridoma (clone #6) supernatant using protein A agarose. This hybridoma was established by fusion of mouse myeloma cell SP2/0 with Balb/c mouse splenocyte immunized with purified human IFN-γ.

Documents

References

1) Ferrar, M. A., et al., Annu. Rev. Immunol. 11, 571-611 (1993) 2) Sen, G. C., et al., J. Biol. Chem. 267, 5017-5020 (1992) 3) Kawabe, Y., et al., J. IFN. Res. 4, 571-584 (1984)