Interferon gamma ELISA Kit

Produktnummer ABIN6963446

Produktdetails Interferon gamma ELISA Kit

Target: Interferon gamma (IFNG)

Reaktivität: Human

Nachweismethode: Colorimetric

Methodentyp: Sandwich ELISA

Detektionsbereich: 15.63 pg/mL - 1000 pg/mL

Untere Nachweisgrenze: 15.63 pg/mL

Applikation: ELISA

Verwendungszweck: The kit is a sandwich enzyme immunoassay technique for the in vitro quantitative measurement in various sample types.

Proben: Cell Culture Supernatant, Plasma, Serum

Analytische Methode: Quantitative

Spezifität: This kit recognizes Human IFN-γ in samples. No Significant cross-reactivity or interference between Human IFN-γ and analogues was observed.

Sensitivität: 9.38 pg/mL

Bestandteile:

• Pre-coated, ready to use 96-well strip plate, flat buttom
• Plate sealer for 96 wells
• Reference Standard
• Reference Standard & Sample Diluent
• Biotinylated Detection Antibody (100 x concentrate)
• HRP Conjugate (100 x concentrate)
• Biotinylated Detection Antibody Diluent
• HRP Conjugate Diluent
• Substrate Reagent
• Stop Solution
• Wash Buffer (25 x concentrate)
• Instruction manual

Anwendungsinformationen

Probenmenge: 100 μL

Testdauer: 3.5 h

Plattentyp: Pre-coated

Protokoll:

1. Add 100 µL standard or sample to each well. Incubate for 90 min at 37 °C.
2. Remove the liquid. Add 100 µL Biotinylated Detection Antibody. Incubate for 1 hour at 37 °C.
3. Aspirate and wash 3 times.
4. Add 100 µL HRP Conjugate. Incubate for 30 min at 37 °C.
5. Aspirate and wash 5 times.
6. Add 90 µL Substrate Reagent. Incubate for 15 min at 37 °C.
7. Add 50 µL Stop Solution. Read at 450 nm immediately.
8. Calculation of results.

Aufbereitung der Reagenzien:

1. Bring all reagents to room temperature (18~25 °C) before use. Follow the Microplate reader manual for set-up and preheat it for 15 min before OD measurement.
2. Wash Buffer: Dilute 30 mL of Concentrated Wash Buffer with 720 mL of deionized or distilled water to prepare 750 mL of Wash Buffer.Note: if crystals have formed in the concentrate, warm it in a 40 °C water bath and mix it gently until the crystals have completely dissolved
3. Standard working solution: Centrifuge the standard at 10,000xg for 1 min. Add 1.0 mL of Reference Standard &Sample Diluent, let it stand for 10 min and invert it gently several times. After it dissolves fully, mix it thoroughly with a pipette. This reconstitution produces a working solution of 1000 pg/mL. Then make serial dilutions as needed. The recommended dilution gradient is as follows: 1000, 500, 250, 125, 62.5, 31.25, 15.63, 0 pg/mL. Dilution method: Take 7 EP tubes, add 500 μLof Reference Standard & Sample Diluent to each tube. Pipette 500 μLof the 1000 pg/mL working solution to the first tube and mix up to produce a 500 pg/mL working solution. Pipette 500 μLof the solution from the former tube into the latter one according to these steps. The illustration below is for reference. Note: the last tube is regarded as a blank. Don't pipette solution into it from the former tube.
4. Biotinylated Detection Antibody working solution: Calculate the required amount before the experiment (100 μL/well). In preparation, slightly more than calculated should be prepared. Centrifuge the stock tube before use, dilute the 100x Concentrated Biotinylated Detection Antibody to 1xworking solution with Biotinylated Detection Antibody Diluent.
5. Concentrated HRP Conjugate working solution: Calculate the required amount before the experiment (100 μL/well). In preparation, slightly more than calculated should be prepared. Dilute the 100x Concentrated HRP Conjugate to 1x working solution with Concentrated HRP Conjugate Diluent.

Aufbereitung der Proben:

• It is recommended to use fresh samples without long storage, otherwise protein degradation and denaturation may occur in these samples, leading to false results. Samples should therefore be stored for a short period at 2 - 8 °C or aliquoted at -20 °C (≤1 month) or -80 °C (≤ 3 months). Repeated freeze-thaw cycles should be avoided. Prior to assay, the frozen samples should be slowly thawed and centrifuged to remove precipitates.
• If the sample type is not specified in the instructions, a preliminary test is necessary to determine compatibility with the kit.
• If a lysis buffer is used to prepare tissue homogenates or cell culture supernatant, there is a possibility of causing a deviation due to the introduced chemical substance. The recommended dilution factor is for reference only.
• Please estimate the concentration of the samples before performing the test. If the values are not in the range of the standard curve, the optimal sample dilution for the particular experiment has to be determined.

Testpräzision: Intra-assay Precision (Precision within an assay): 3 samples with low, mid range and high level Human IFN-γ were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, mid range and high level Human IFN-γ were tested on 3 different plates, 20 replicates in each plate.
Both intra-CV and inter-CV are < 10 %.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung:

1. For unopened kit: All reagents should be stored according to the labels on the vials, so they are stable up to 12 months after receipt of the kit. The Reference Standard, Biotinylated Detection Antibody, HRP Conjugate and the 96-well stripe plate should be stored at -20 °C upon receipt while the other reagents should be stored at 4 °C.
2. For used kit: When the kit is used, the remaining reagents need to be stored according to the above storage condition. Besides, please return the unused wells to the foil pouch containing the desiccant pack, and zip-seal the foil pouch.

Haltbarkeit: 12 months

Referenzen für Interferon gamma ELISA Kit (ABIN6963446)

Rakhra, Masih, Vats, Vijay, Ashraf, Singh: "Study of Metal-Metal Interactions and Their Biomarkers Using an Intestinal Human Cell Line." in: Biological trace element research, Vol. 195, Issue 1, pp. 95-104, (2021) (PubMed).

Ma, Liang, Chen, Wang, Li, Liang, Wang, Tian, Yang, Niu: "Glutamine Deprivation Induces PD-L1 Expression via Activation of EGFR/ERK/c-Jun Signaling in Renal Cancer." in: Molecular cancer research : MCR, Vol. 18, Issue 2, pp. 324-339, (2020) (PubMed).

Öztürk, Yalın Sapmaz, Kandemir, Taneli, Aydemir: "The role of the kynurenine pathway and quinolinic acid in adolescent major depressive disorder." in: International journal of clinical practice, pp. e13739, (2020) (PubMed).

Lejeune, Mordacq, Drumez, Brisset, Pouessel, Pichavant, Engelmann, Béghin, Decleyre-Badiu, Neve, Thumerelle, Gosset, Deschildre: "Relationship between immune parameters during a severe exacerbation in allergic asthmatic children and asthma outcomes in the following year." in: Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology, Vol. 50, Issue 3, pp. 406-411, (2020) (PubMed).

Zheng, Sun, Xu, Pan, Zhang, Fang, Fang, Cai: "Clinical characteristics of 34 COVID-19 patients admitted to intensive care unit in Hangzhou, China." in: Journal of Zhejiang University. Science. B, Vol. 21, Issue 5, pp. 378-387, (2020) (PubMed).

Al-Hakami, Alqhatani, Shaik, Jalfan, Dhammam, Asiri, Alkahtani, Devaraj, Chandramoorthy: "Cytokine physiognomies of MSCs from varied sources confirm the regenerative commitment post-coculture with activated neutrophils." in: Journal of cellular physiology, Vol. 235, Issue 11, pp. 8691-8701, (2020) (PubMed).

Li, Zhang, Wang, Zhao, Zhang, Ding, Wei: "Aging affects responsiveness of peripheral blood mononuclear cells to immunosuppression of periodontal ligament stem cells." in: The Journal of international medical research, Vol. 48, Issue 7, pp. 300060520930853, (2020) (PubMed).

Kilanczyk, Banales, Wunsch, Barbier, Avila, Mato, Milkiewicz, Milkiewicz: "S-adenosyl-L-methionine (SAMe) halts the autoimmune response in patients with primary biliary cholangitis (PBC) via antioxidant and S-glutathionylation processes in cholangiocytes." in: Biochimica et biophysica acta. Molecular basis of disease, Vol. 1866, Issue 11, pp. 165895, (2020) (PubMed).

Li, Dong, Huang, Chen, Kong, Sun, Yu, Xu: "Clonorchis sinensis Co-infection Could Affect the Disease State and Treatment Response of HBV Patients." in: PLoS neglected tropical diseases, Vol. 10, Issue 6, pp. e0004806, (2017) (PubMed).

Details zu Interferon gamma

Target: Interferon gamma (IFNG)

Andere Bezeichnung: Interferon Gamma (IFNG Produkte)

Synonyme: IFG ELISA Kit, IFI ELISA Kit, IFN-g ELISA Kit, Ifg ELISA Kit, IFNG2 ELISA Kit, IFN-gamma ELISA Kit, IFN-G ELISA Kit, IFNG ELISA Kit, IFNgamma ELISA Kit, TCRalpha ELISA Kit, INF-G ELISA Kit, ifng ELISA Kit, interferon gamma ELISA Kit, interferon, gamma 1-2 ELISA Kit, IFNG ELISA Kit, Ifng ELISA Kit, ifng1-2 ELISA Kit

Hintergrund: IFNG, IFG, IFI, Type II Interferon

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, Autophagie