CD40 Human, IgG2a Fc Mouse, Fusion Protein (PE)

Cat# C2392-02L-50T

Size : 50Tests

Brand : US Biological

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C2392-02L CD40 Human, IgG2a Fc Mouse, Fusion Protein (PE)

Clone Type
Polyclonal
Grade
Affinity Purified
Applications
FC
Shipping Temp
Blue Ice
Storage Temp
4°C Do Not Freeze

Human CD40 is a member of the tumor necrosis factor (TNF) receptor family and is present on all B cells except plasma cells. CD40 is also found on some epithelial cells, carcinomas and lymphoid dendritic cells. CD40 plays an important role in B cell activation and the interaction with its ligand CD154 (CD40 Ligand) is essential for isotype switching (1). CD40 muIg fusion protein is recognized by anti-human CD40 antibody and binds to human CD154. This binding can be blocked by anti-CD154 antibody.||Molecular Structure: |A soluble fusion protein consisting of the extracellular (193aa) domain of human CD40 fused to murine IgG2a Fc (232aa), with a predicted monomeric molecular weight of 45.6kD.||Applications: |Suitable for use in ELISA and Flow Cytometry. Other applications not tested.||Functional Application: |CD40-muIg fusion protein is recognized by anti-human CD40 (C2392-02E). This binding can be blocked by using anti-human CD154 (C2548-84W1).||Recommended Dilutions:|Flow Cytometry: 1:20 (20ug/ml). 80ul of diluted solution labels 5x10e5 cells.|Optimal dilutions to be determined by the researcher.||Storage and Stability:|Store product at 4°C in the dark. DO NOT FREEZE! Stable at 4°C for 6 months after receipt as an undiluted liquid. Dilute required amount only prior to immediate use. Further dilutions can be made in assay buffer. Caution: PE conjugates are sensitive to light. For maximum recovery of product, centrifuge the original vial prior to removing the cap.||Flow Cytometry Protocol:|1. Ficoll prepared human peripheral blood mononuclear cells were stimulated 6 hours in the presence of 10ng/ml PMA and 1uM Ionomicin to upregulate CD154 expression. |2. Five x 10e5 cells per tube were washed and incubated for 45 minutes on ice with 80ul of a 1:20 dilution (20ug/ml) of C2392-02L. |3. They were washed three times, fixed and analyzed by Flow Cytometry. |4. A 39% sub-population of the cells stained positive with a mean shift of 1.16 log10 fluorescent units when compared to a negative control.|5. Binding was effectively blocked when cells were preincubated 10 minutes with 20ul of 0.5mg/ml anti-CD154 antibody (C2548-84W1).

Applications
Source: CHO cells|Purity: Purified by Protein A affinity chromatography from tissue culture supernatant.|Concentration: ~0.4mg/ml|Form: Supplied as a liquid in 50mM sodium phosphate pH 7.5, 500mM potassium chloride, 150mM sodium chloride, 0.2% BSA, 0.04% sodium azide, 15% glycerol. Labeled with R-Phycoerythrin (PE). A565/A280=3.59.||Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.
Form
Supplied as a liquid in 50mM sodium phosphate pH 7.5, 500mM potassium chloride, 150mM sodium chloride, 0.2% BSA, 0.04% sodium azide, 15% glycerol. Labeled with R-Phycoerythrin (PE). A565/A280=3.78.
Purity
Purified by Protein A affinity chromatography from tissue culture supernatant.
References
1. T.A. Foy, et al, (1996) Annu Rev Immunol 14: 591-617. 2. M.E. Ozaki, et al, (1997) J Immunol 159: 214-221.