Rhesus Monkey IFNG ELISA Kit, Lot 21AO-1018 [Cancer Immune Checkpoint Assay Kit]

CAT#: IOK-05-P929
Product Type: ELISA Kit
Target: IFNG
Short Description
The kit is designed for in vitro quantitative measurement of Rhesus Monkey IFNG in Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Homogenate.
Description
The kit is a sandwich enzyme immunoassay for the in vitro quantitative measurement of IFNg in monkey serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.
Applications
ELISA
Target
IFNG
Reactivity
Rhesus Monkey
Detection Method
Colorimetric
Method Type
Sandwich ELISA
Analytical Method
Quantitative
Sample Type
Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Homogenate
Specificity
This assay has high sensitivity and excellent specificity for detection of this index.
Cross-Reactivity
No significant cross-reactivity or interference between this index and analogues was observed. Note: Limited by current skills and knowledge, it is impossible for us to complete the cross- reactivity detection between this index and all the analogues, therefore, cross reaction may still exist.
Components
Pre-coated, ready to use 96-well strip plate
Plate sealer for 96 wells
Standard
Standard Diluent
Detection Reagent A
Detection Reagent B
Assay Diluent A
Assay Diluent B
TMB Substrate
Stop Solution
Wash Buffer (30 x concentrate)
Instruction manual
Material not included
1.Microplate reader with 450 ± 10nm filter.
2.Precision single or multi-channel pipettes and disposable tips.
3.Tubes for diluting samples.
4.Deionized or distilled water.
5.Absorbent paper for blotting the microtiter plate.
6.Container for Wash Solution.
7.0.01Mol/L (or 1x) Phosphate Buffered Saline(PBS), pH 7.0-7.2.
Sensitivity
6.1 pg/mL
Sample Volume
100 μL
Assay Time
1 - 4.5 h
Plate
Pre-coated
Assay Procedure
1.Add 100μL each of dilutions of standard, blank and samples into the appropriate wells, respectively. Cover with the Plate sealer. Incubate for 1 hour at 37 °C.
2.Remove the liquid of each well, don't wash.
3.Add 100μL of Detection Reagent A working solution to each well, cover the wells with the plate sealer and incubate for 1 hour at 37 °C.
4.Aspirate the solution and wash with 350μL of 1x Wash Solution to each well and let it sit for 1-2 minutes. Remove the remaining liquid from all wells completely by snapping the plate onto absorbent paper. Totally wash 3 times. Invert the plate and blot it against absorbent paper.
5.Add 100μL of Detection Reagent B working solution to each well, cover the wells with the plate sealer and incubate for 30 minutes at 37 °C.
6.Repeat the aspiration/wash process for total 5 times as conducted in step 4.
7.Add 90μL of Substrate Solution to each well. Cover with a new Plate sealer. Incubate for 10 - 20 minutes at 37 °C. Protect from light.
8.Add 50μL of Stop Solution to each well. Mix the liquid by tapping the side of the plate.
9.Remove any drop of water and fingerprint on the bottom of the plate. Then, run the microplate reader and conduct measurement at 450nm immediately.
Assay Precision
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level of target were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level of target were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV < 10%
Inter-Assay: CV < 12%
Precaution of Use
The Stop Solution suggested for use with this kit is an acid solution. Wear eye, hand, face, and clothing protection when using this material.
Handling Advice
The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5 % within the expiration date under appropriate storage conditions.
Storage
4 °C,-20 °C
Storage Comment
The Assay Plate, Standard, Detection Reagent A and Detection Reagent B should be stored at -20°C upon being received. After receiving the kit , Substrate should be always stored at 4°C.Other reagents are kept according to the labels on vials. But for long term storage, please keep the whole kit at -20°C. The unused strips should be kept in a sealed bag with the desiccant provided to minimize exposure to damp air.
Expiry Date
12 months
Note
The Assay Plate, Standard, Detection Reagent A and Detection Reagent B should be stored at -20°C upon being received. After receiving the kit , Substrate should be always stored at 4°C.Other reagents are kept according to the labels on vials. But for long term storage, please keep the whole kit at -20°C. The unused strips should be kept in a sealed bag with the desiccant provided to minimize exposure to damp air.
Restrictions
For Research Use only
Alternative Name
Interferon gamma
Synonyms
IFG; IFI; IFN-g; Ifg; IFNG2; IFN-gamma; IFN-G; IFNG; IFNgamma; TCRalpha; INF-G; ifng; interferon gamma; interferon; gamma 1-2; IFNG; Ifng; ifng1-2
Background
Alternative name: IFN-G, IFG, IFI, INFr, IFN, Immune Interferon
Gene ID
102128291
UniProt
P63309
Pathways
Interferon-gamma Pathway, Cellular Response to Molecule of Bacterial Origin, Regulation of Leukocyte Mediated Immunity, Positive Regulation of Immune Effector Process, Production of Molecular Mediator of Immune Response, ER-Nucleus Signaling, Regulation of Carbohydrate Metabolic Process, Protein targeting to Nucleus, Autophagy
Protocol
1.Prepare all reagents, samples and standards.
2.Add 100μL standard or sample to each well. Incubate 1 hours at 37 °C.
3.Aspirate and add 100μL prepared Detection Reagent A. Incubate 1 hour at 37 °C.
4.Aspirate and wash 3 times.
5.Add 100μL prepared Detection Reagent B. Incubate 30 minutes at 37 °C.
6.Aspirate and wash 5 times.
7.Add 90μL Substrate Solution. Incubate 10-20 minutes at 37 °C.
8.Add 50μL Stop Solution. Read at 450nm immediately.
For Research Use Only | Not For Clinical Use
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