Human Interferon gamma Recombinant Rabbit Monoclonal Antibody [PSH01-47]
cat.: HA721685
| Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
|---|---|
| Species reactivity: | Human |
| Applications: | ELISA(Det) |
| Clonality: | Monoclonal |
| Clone number: | PSH01-47 |
| Form: | Liquid |
| Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles. |
| Storage buffer: | PBS (pH7.4). |
| Concentration: | 1ug/ul |
| Purification: | Protein A affinity purified. |
| Molecular weight: | 19.3 |
| Isotype: | IgG |
| Immunogen: | Recombinant protein within human Interferon gamma aa 24-161. |
| Positive control: | Recombinant Human Interferon gamma protein (HA210762). |
| Subcellular location: | Secreted. |
| Recommended Dilutions:
ELISA(Det) |
Use at an assay dependent concentration. Can be paired for Sandwich ELISA with Rabbit monoclonal [PSH01-45] or [PSH01-46]to Human Human Interferon gamma (Capture) (HA721683) or (HA721684). |
| Uniprot #: | SwissProt: P01579 Human |
| Alternative names: | IF 1 IFG IFI ifn g IFN gamma IFN immune IFN, immune IFN-gamma IFNG IFNG_HUMAN Immune interferon Interferon gamma Type II Interferon |
Images
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Fig1:
Standard curve of human IFNG matched pair antibodies: Sandwich ELISA analysis of human IFNG matched pair antibodies Elisa assay was performed by coating wells of a 96-well plate with 100 µl per well of capture antibody [PSH01-45] diluted in carbonate/bicarbonate buffer, at a concentration of 4 µg/mL overnight at 4℃. Wells of the plate were washed, blocked with 150 µl 0.05% tween-20 1%BSA blocking buffer, and incubated with serial diluted IFNG protein starting from 2500 pg/ml to 0 pg/ml and detect antibody [PSH01-47]-Biotin (0.2 µg/ml) for 1 hour at 30℃ with shaking. Then the plate was washed and incubated with 100 µl per well of SA-HRP for 0.5 hour at 30℃ with shaking. Detection was performed using an Ultra TMB Substrate for 10 minutes at room temperature in the dark. The reaction was stopped with sulfuric acid and absorbances were read on a spectrophotometer at 450 nm. |
|
Fig2:
Standard curve of human IFNG matched pair antibodies: Sandwich ELISA analysis of human IFNG matched pair antibodies Elisa assay was performed by coating wells of a 96-well plate with 100 µl per well of capture antibody [PSH01-46] diluted in carbonate/bicarbonate buffer, at a concentration of 4 µg/mL overnight at 4℃. Wells of the plate were washed, blocked with 150 µl 0.05% tween-20 1%BSA blocking buffer, and incubated with serial diluted IFNG protein starting from 2500 pg/ml to 0 pg/ml and detect antibody [PSH01-47]-Biotin (0.2 µg/ml) for 1 hour at 30℃ with shaking. Then the plate was washed and incubated with 100 µl per well of SA-HRP for 0.5 hour at 30℃ with shaking. Detection was performed using an Ultra TMB Substrate for 10 minutes at room temperature in the dark. The reaction was stopped with sulfuric acid and absorbances were read on a spectrophotometer at 450 nm. |
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.