IL-6 Kit ELISA

N° du produit ABIN365191

Détail du produit IL-6 Kit ELISA

Antigène: IL-6 (IL6) (Interleukin 6 (IL6))

Reactivité: Rat

Méthode de détection: Colorimetric

Type de méthode: Sandwich ELISA

Gamme de detection: 0.312-20 pg/mL

Seuil minimal de détection: 0.312 pg/mL

Application: ELISA

Fonction: For the quantitative determination of rat interleukin 6 (IL-6) concentrations in serum, plasma, cell culture supernates, tissue homogenates, cell lysates.

Type d'échantillon: Plasma, Serum, Tissue Homogenate

Analytical Method: Quantitative

Specificité: This assay has high sensitivity and excellent specificity for detection of rat IL-6.

Réactivité croisée (Details): Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between the target antigen and all analogues for other species. Therefore, cross reaction may still exist.

Sensibilité: 0.078 pg/mL

Ingrédients:

• Assay plate (12 × 8 coated Microwells)
• Standard (freeze dried)
• Biotin-antibody (100 × concentrate)
• HRP-avidin (100 × concentrate)
• Biotin-antibody Diluent
• HRP-avidin Diluent
• Sample Diluent
• Wash Buffer (25 × concentrate)
• TMB Substrate
• Stop Solution
• Adhesive Strip (for 96 wells)
• Instruction manual

Information d'application

Indications d'application:

• The supplier is only responsible for the kit itself, but not for the samples consumed during the assay. The user should calculate the possible amount of the samples used in the whole test. Please reserve sufficient samples in advance.
• Samples to be used within 5 days may be stored at 2-8°C, otherwise samples must be stored at -20°C (≤ 1 month) or -80°C (≤ 2 months) to avoid loss of bioactivity and contamination.
• Grossly hemolyzed samples are not suitable for use in this assay.
• If the samples are not indicated in the manual, a preliminary experiment to determine the validity of the kit is necessary.
• Please predict the concentration before assaying. If values for these are not within the range of the standard curve, users must determine the optimal sample dilutions for their particular experiments.
• Tissue or cell extraction samples prepared by chemical lysis buffer may cause unexpected ELISA results due to the impacts of certain chemicals.
• Owing to the possibility of mismatching between antigens from another resource and antibodies used in this supplier's kits (e.g., antibody targets conformational epitope rather than linear epitope), some native or recombinant proteins from other manufacturers may not be recognized by this supplier's products.
• Influenced by factors including cell viability, cell number and cell sampling time, samples from cell culture supernatant may not be recognized by the kit.
• Fresh samples without long time storage are recommended for the test. Otherwise, protein degradation and denaturalization may occur in those samples and finally lead to wrong results.

Commentaires:

Detection wavelength: 450 nm

Information on standard material:
Depending on the antigen to be detected, standards can be either native or recombinant protein. The recombinant proteins are being expressed in CHO cells in most cases. Please inquire for more information. The formulation of auxiliary material in the standard is considered proprietary information, however it does not contain any poisonous substance. Proclin 300 (1:3000) is used as preservative.

Information on reagents:
In most cases the stop solution provided is 1 N H2SO4. The formulation of wash solution is proprietary information. None of the components contain (sodium) azide, thimerosal, 2-mercaptoethanol (2-ME) or any other poisonous materials. For the sandwich method kits, the sample diluent, antibody diluent, enzyme diluent and standard all contain BSA.

Information on antibodies:
The antibodies provided in different kits vary in regards to clonality and host. Some antibodies are affinity purified, some are Protein A

Volume d'échantillon: 100 μL

Durée du test: 1 - 4.5 h

Plaque: Pre-coated

Protocole: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for IL-6 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any IL-6 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for IL-6 is added to the wells. After washing, avidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of IL-6 bound in the initial step. The color development is stopped and the intensity of the color is measured.

Préparation des réactifs:

• Biotin-antibody (1×) - Centrifuge the vial before opening.
  Biotin-antibody requires a 100-fold dilution. The suggested dilution is 10µL of Biotin-antibody + 990µL of Biotin-antibody Diluent.
• HRP-avidin (1×) - Centrifuge the vial before opening.
  HRP-avidin requires a 100-fold dilution. The suggested dilution is 10µL of HRP-avidin + 990µL of HRP-avidin Diluent.
• Wash Buffer (1×) - If crystals have formed in the concentrate, warm up to room temperature and mix gently until the crystals have completely dissolved. Dilute 20mL of Wash Buffer Concentrate (25×) into deionized or distilled water to prepare 500mL of Wash Buffer (1×).
• Standard - Centrifuge the standard vial at 6000-10000rpm for 30s.
  Reconstitute the Standard with 1ml of Sample Diluent. Do not substitute other diluents. This reconstitution produces a stock solution. Mix the standard to ensure complete reconstitution and allow the standard to sit for a minimum of 15 minutes with gentle agitation prior to making dilutions.
  Pipette 250µL of Sample Diluent into each tube. Use the stock solution to produce a 2-fold dilution series. Mix each tube thoroughly before the next transfer. The undiluted Standard serves as the high standard. Sample Diluent serves as the zero standard (0ng/mL).

Note:

• Kindly use graduated containers to prepare the reagent. Please don't prepare the reagent directly in the Diluent vials provided in the kit.
• Bring all reagents to room temperature (18-25°C) before use for 30 min.
• Prepare fresh standard for each assay. Use within 4 hours and discard after use.
• Making serial dilution in the wells directly is not permitted.
• Please carefully reconstitute Standards according to the instruction. Avoid foaming and mix gently until the crystals have completely dissolved. To minimize imprecision caused by pipetting, use small volumes and ensure that pipettors are calibrated. It is recommended to suck more than 10µL when pipetting.
• It is recommended to use distilled water to prepare reagents and samples. Using contaminated water or container for reagent preparation will influence detection result.

Précision du teste: Intra-assay precision (precision within an assay): Three samples of known concentration were tested twenty times on one plate to assess precision.
Inter-assay precision (precision between assays): Three samples of known concentration were tested in twenty assays to assess precision.

• Intra-assay: CV% less than 8%
• Inter-assay: CV% less than 10%

Restrictions: For Research Use only

Stockage

Précaution d'utilisation: The Stop Solution provided with this kit is an acid solution. Wear eye, hand, face and clothing protection when using this material.

Conseil sur la manipulation:

• The kit should not be used beyond the expiration date on the kit label.
• Do not mix or substitute reagents with those from other lots or sources.
• If samples generate values higher than the highest standard, dilute the samples with Sample Diluent and repeat the assay.
• Any variation in Sample Diluent, operator, pipetting technique, washing technique, incubation time/temperature and kit age can cause variation in binding.
• This assay is designed to eliminate interference by soluble receptors, binding proteins and other factors present in biological samples. Until all factors have been tested in the Immunoassay, the possibility of interference cannot be excluded.

Stock: 4 °C/-20 °C

Stockage commentaire: For unopened kit: All the reagents should be kept according to the labels on vials.

Date de péremption: 6 months

Références pour IL-6 Kit ELISA (ABIN365191)

Nair, Gagnon, Pelletier, Tchoukanova, Zhang, Ewart, Ewart, Jiao, Wang: "Shrimp oil extracted from the shrimp processing waste reduces the development of insulin resistance and metabolic phenotypes in diet-induced obese rats." dans: Applied physiology, nutrition, and metabolism = Physiologie appliquée, nutrition et métabolisme, Vol. 42, Issue 8, pp. 841-849, (2018) (PubMed).

Adamu, Imam, Der-Jiun, Ismail: "In utero Exposure to Germinated Brown Rice and Its GABA Extract Attenuates High-Fat-Diet-Induced Insulin Resistance in Rat Offspring." dans: Journal of nutrigenetics and nutrigenomics, Vol. 10, Issue 1-2, pp. 19-31, (2018) (PubMed).

Wang, Ding, Tang, Li, Gan: "Effect of Liuweibuqi capsules on the balance between MMP-9 and TIMP1 and viability of alveolar macrophages in COPD." dans: Bioscience reports, Vol. 37, Issue 5, (2018) (PubMed).

Wang, Yi, Du, Wang, Tang, Wang, Qi, Li, Lai, Xia, Tang: "A study of Epstein-Barr virus infection in the Chinese tree shrew(Tupaia belangeri chinensis)." dans: Virology journal, Vol. 14, Issue 1, pp. 193, (2018) (PubMed).

Chen, Zhang, Zhang, He, Zhou, Xie: "Dexmedetomidine reduces the neuronal apoptosis related to cardiopulmonary bypass by inhibiting activation of the JAK2-STAT3 pathway." dans: Drug design, development and therapy, Vol. 11, pp. 2787-2799, (2018) (PubMed).

Nielsen, Roager, Casas, Frandsen, Gosewinkel, Bester, Licht, Hendriksen, Bahl: "Glyphosate has limited short-term effects on commensal bacterial community composition in the gut environment due to sufficient aromatic amino acid levels." dans: Environmental pollution (Barking, Essex : 1987), Vol. 233, pp. 364-376, (2018) (PubMed).

Zhao, Zhang, Ma, Tian, Shen, Zhou: "A combination of quercetin and resveratrol reduces obesity in high-fat diet-fed rats by modulation of gut microbiota." dans: Food & function, Vol. 8, Issue 12, pp. 4644-4656, (2018) (PubMed).

Eltahir, Nazmy: "Esomeprazole ameliorates CCl4 induced liver fibrosis in rats via modulating oxidative stress, inflammatory, fibrogenic and apoptotic markers." dans: Biomedicine & pharmacotherapy, Vol. 97, pp. 1356-1365, (2018) (PubMed).

Abbas, Kamel, El-Sayed: "Dermal anti-oxidant, anti-inflammatory and anti-aging effects of Compritol ATO-based Resveratrol colloidal carriers prepared using mixed surfactants." dans: International journal of pharmaceutics, Vol. 541, Issue 1-2, pp. 37-47, (2018) (PubMed).

Chepurnova, Samoilova, Anisimov, Verin, Korotaeva: "Compounds of IL-6 Receptor Complex during Acute Lung Injury." dans: Bulletin of experimental biology and medicine, Vol. 164, Issue 5, pp. 609-611, (2018) (PubMed).

Li, Li, Liu, Wang, Zhang, Li, Yang, Song, Yin, Gao, Cheng, Cai, Tian: "Telmisartan Ameliorates Nephropathy in Metabolic Syndrome by Reducing Leptin Release From Perirenal Adipose Tissue." dans: Hypertension (Dallas, Tex. : 1979), Vol. 68, Issue 2, pp. 478-90, (2017) (PubMed).

Wang, Cui, Chen, Deng, Liao, Wei, Li, Su, Yu, Yi: "Prenatal Exposure to Lipopolysaccharide Alters Renal DNA Methyltransferase Expression in Rat Offspring." dans: PLoS ONE, Vol. 12, Issue 1, pp. e0169206, (2017) (PubMed).

Xie, Min, Chen, Yang, Wang: "Ulinastatin inhibited sepsis-induced spinal inflammation to alleviate peripheral neuromuscular dysfunction in an experimental rat model of neuromyopathy." dans: Journal of neurochemistry, Vol. 143, Issue 2, pp. 225-235, (2017) (PubMed).

Xie, Xiao, Luo, Fu, Wang, Wang, Liang, Luo: "Integrating qualitative and quantitative characterization of traditional Chinese medicine injection by high-performance liquid chromatography with diode array detection and tandem mass spectrometry." dans: Journal of separation science, Vol. 37, Issue 12, pp. 1438-47, (2016) (PubMed).

Tang, Yang, Zhang, Ren, Sang, Lu, Zhong, Mao: "Magnesium isoglycyrrhizinate inhibits inflammatory response through STAT3 pathway to protect remnant liver function." dans: World journal of gastroenterology, Vol. 21, Issue 43, pp. 12370-80, (2016) (PubMed).

Adamu, Imam, Ooi, Esa, Rosli, Ismail: "Perinatal exposure to germinated brown rice and its gamma amino-butyric acid-rich extract prevents high fat diet-induced insulin resistance in first generation rat offspring." dans: Food & nutrition research, Vol. 60, pp. 30209, (2016) (PubMed).

Guo, Ding, Huang, Wang, Meng, Xiao: "Total saponin of Dioscoreae hypoglaucae rhizoma ameliorates streptozotocin-induced diabetic nephropathy." dans: Drug design, development and therapy, Vol. 10, pp. 799-810, (2016) (PubMed).

Abdul Shukkoor, Baharuldin, Mat Jais, Mohamad Moklas, Fakurazi: "Antidepressant-Like Effect of Lipid Extract of Channa striatus in Chronic Unpredictable Mild Stress Model of Depression in Rats." dans: Evidence-based complementary and alternative medicine : eCAM, Vol. 2016, pp. 2986090, (2016) (PubMed).

Mohammad Reza, Hamideh, Zahra: "The Nociceptive and Anti-Inflammatory Effects of Artemisia dracunculus L. Aqueous Extract on Fructose Fed Male Rats." dans: Evidence-based complementary and alternative medicine : eCAM, Vol. 2015, pp. 895417, (2015) (PubMed).

Zhang, Li, Jiang, Chen, Huang: "Neuroprotective Effects of (-)-Epigallocatechin-3-Gallate Against Focal Cerebral Ischemia/Reperfusion Injury in Rats Through Attenuation of Inflammation." dans: Neurochemical research, Vol. 40, Issue 8, pp. 1691-8, (2015) (PubMed).

Détail du antigène

Antigène: IL-6 (IL6) (Interleukin 6 (IL6))

Autre désignation: Interleukin 6 (IL-6) (IL6 Produits)

Synonymes: BSF2 Kit ELISA, HGF Kit ELISA, HSF Kit ELISA, IFNB2 Kit ELISA, IL-6 Kit ELISA, Il-6 Kit ELISA, ILg6 Kit ELISA, Ifnb2 Kit ELISA, il6 Kit ELISA, CHIL-6 Kit ELISA, interleukin 6 Kit ELISA, interleukin-6 Kit ELISA, IL6 Kit ELISA, Il6 Kit ELISA, il-6 Kit ELISA, IL-6 Kit ELISA

Sujet: Synonyms: BSF2, HGF, HSF, IFNB2, IL-6, B cell stimulatory factor-2|B-cell differentiation factor|CTL differentiation factor|OTTHUMP00000158544|hybridoma growth factor|interleukin 6|interleukin BSF-2

HGNC: 1834

UniProt: Q9MZR1

Pathways: Signalisation TLR, Hormone Transport, Negative Regulation of Hormone Secretion, Myometrial Relaxation and Contraction, Positive Regulation of Immune Effector Process, Production of Molecular Mediator of Immune Response, Regulation of Carbohydrate Metabolic Process, Autophagy, Cell RedoxHomeostasis, Cancer Immune Checkpoints, Inflammasome