Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

NOS2 ELISA Kit

NOS2 Reactivity: Mouse Colorimetric Sandwich ELISA 0.31 ng/mL - 20 ng/mL Cell Culture Supernatant, Cell Lysate, Tissue Homogenate
Catalog No. ABIN7066936
  • Target See all NOS2 ELISA Kits
    NOS2 (Nitric Oxide Synthase 2, Inducible (NOS2))
    Reactivity
    • 8
    • 6
    • 6
    • 4
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Mouse
    Detection Method
    Colorimetric
    Method Type
    Sandwich ELISA
    Detection Range
    0.31 ng/mL - 20 ng/mL
    Minimum Detection Limit
    0.31 ng/mL
    Application
    ELISA
    Purpose
    The kit is a sandwich enzyme immunoassay for in vitro quantitative measurement of NOS2 in mouse tissue homogenates, cell lysates, cell culture supernates.

    We offer validation data (WB) for the kit components. So you can be sure to order a reliable ELISA kit product composed of high quality reagents.
    Sample Type
    Cell Culture Supernatant, Cell Lysate, Tissue Homogenate
    Analytical Method
    Quantitative
    Specificity
    This assay has high sensitivity and excellent specificity for detection of Nitric Oxide Synthase 2, Inducible (NOS2)
    Cross-Reactivity (Details)
    No significant cross-reactivity or interference between Nitric Oxide Synthase 2, Inducible (NOS2) and analogues was observed.
    Sensitivity
    0.116 ng/mL
    Components
    • Pre-coated, ready to use 96-well strip plate, flat buttom
    • Plate sealer for 96 wells
    • Reference Standard
    • Standard Diluent
    • Detection Reagent A
    • Detection Reagent B
    • Assay Diluent A
    • Assay Diluent B
    • Reagent Diluent (if Detection Reagent is lyophilized)
    • TMB Substrate
    • Stop Solution
    • Wash Buffer (30 x concentrate)
    • Instruction manual
  • Comment

    Information on standard material:
    The standard might be recombinant protein or natural protein, that will depend on the specific kit. Moreover, the expression system is E.coli or yeast or mammal cell. There is 0.05% proclin 300 in the standard as preservative.

    Information on reagents:
    The stop solution used in the kit is sulfuric acid with concentration of 1 mol/L. And the wash solution is TBS. The standard diluent contains 0.02 % sodium azide, assay diluent A and assay diluent B contain 0.01% sodium azide. Some kits can contain is BSA in them.

    Information on antibodies:
    The provided antibodies and their host vary in different kits.

    Sample Volume
    100 μL
    Assay Time
    3 h
    Plate
    Pre-coated
    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.
    Reagent Preparation
    1. Bring all kit components and samples to room temperature (18-25 °C) before use. If the kit will not be used up in one time, please only take out strips and reagents for present experiment, and leave the remaining strips and reagents in required condition.
    2. Standard - Reconstitute the Standard with 1.0 mL of Standard Diluent, keep for 10 minutes at room temperature, shake gently (not to foam). The concentration of the standard in the stock solution is 20 ng/mL. Prepare 7 tubes containing 0.5 mL Standard Diluent and produce a double dilution series. Mix each tube thoroughly before the next transfer. Set up 7 points of diluted standard such as 20 ng/mL, 10 ng/mL, 5 ng/mL, 2.5 ng/mL, 1.25 ng/mL, 0.625 ng/mL, 0.312 ng/mL, and the last microcentrifuge tube with Standard Diluent is the blank as 0 ng/mL.
    3. Detection Reagent A and Detection Reagent B - If lyophilized reconstitute the Detection Reagent A with 150μL of Reagent Diluent, keep for 10 minutes at room temperature, shake gently (not to foam). Briefly spin or centrifuge the stock Detection A and Detection B before use. Dilute them to the working concentration 100-fold with Assay Diluent A and B, respectively.
    4. Wash Solution - Dilute 20 mL of Wash Solution concentrate (30x) with 580 mL of deionized or distilled water to prepare 600 mL of Wash Solution (1x).
    5. TMB substrate - Aspirate the needed dosage of the solution with sterilized tips and do not dump the residual solution into the vial again.

    Note:

    1. Making serial dilution in the wells directly is not permitted.
    2. Prepare standards within 15 minutes before assay. Please do not dissolve the reagents at 37 °C directly.
    3. Please carefully reconstitute Standards or working Detection Reagent A and B according to the instruction, and avoid foaming and mix gently until the crystals are 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 for one pipetting.
    4. The reconstituted Standards, Detection Reagent A and Detection Reagent B can be used only once.
    5. If crystals have formed in the Wash Solution concentrate (30x), warm to room temperature and mix gently until the crystals are completely dissolved.
    6. Contaminated water or container for reagent preparation will influence the detection result.
    Sample Preparation
    • It is recommended to use fresh samples without long storage, otherwise protein degradation and denaturationmay occur in these samples, leading to false results. Samples should therefore be stored for a short periodat 2 - 8 °C or aliquoted at -20 °C (≤1 month) or -80 °C (≤ 3 months). Repeated freeze-thawcycles should be avoided. Prior to assay, the frozen samples should be slowly thawed and centrifuged toremove precipitates.
    • If the sample type is not specified in the instructions, a preliminary test is necessary to determinecompatibility with the kit.
    • If a lysis buffer is used to prepare tissue homogenates or cell culture supernatant, there is a possibilityof 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 therange of the standard curve, the optimal sample dilution for the particular experiment has to be determined.Samples should then be diluted with PBS (pH =7.0-7.2).
    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%
    Restrictions
    For Research Use only
  • 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.
    Storage
    4 °C/-20 °C
    Storage Comment
    1. For unopened kit: All reagents should be stored according to the labels on the vials. The Standard, Detection Reagent A, Detection Reagent B, and 96-well Strip Plate should be stored at -20 °C upon receipt, while the other reagents should be stored at 4 °C.
    2. For opened kits: the remaining reagents must be stored according to the above storage conditions. In addition, please return the unused wells to the foil pouch containing the desiccant and seal the foil pouch with the zipper.
    .
    Expiry Date
    6 months
  • Pan, Zhang, Su, Wang, Liu: "Melatonin Balance the Autophagy and Apoptosis by Regulating UCP2 in the LPS-Induced Cardiomyopathy." in: Molecules (Basel, Switzerland), Vol. 23, Issue 3, (2018) (PubMed).

    Sakthivel, Guruvayoorappan et al.: "Targeted inhibition of tumor survival, metastasis and angiogenesis by Acacia ferruginea mediated regulation of VEGF, inflammatory mediators, cytokine profile and inhibition of transcription factor ..." in: Regulatory toxicology and pharmacology : RTP, Vol. 95, pp. 400-411, (2018) (PubMed).

    Chen, Olatunji, Zhou: "Anti-oxidative, anti-secretory and anti-inflammatory activities of the extract from the root bark of Lycium chinense (Cortex Lycii) against gastric ulcer in mice." in: Journal of natural medicines, Vol. 70, Issue 3, pp. 610-9, (2016) (PubMed).

    Xie, Wen, Yan, Wang, Wang, Chen, Li, Xu, Zhong, Shen, Chu: "Toxoplasma gondii GRA15II effector-induced M1 cells ameliorate liver fibrosis in mice infected with Schistosomiasis japonica." in: Cellular & molecular immunology, (2016) (PubMed).

    Rubila, Ranganathan, Sakthivel: "Protective Effect of Zingiber officinale Against Dalton's Lymphoma Ascites Tumour by Regulating Inflammatory Mediator and Cytokines." in: Applied biochemistry and biotechnology, Vol. 180, Issue 8, pp. 1482-1496, (2016) (PubMed).

    Campo, Avenoso, DAscola, Scuruchi, Calatroni, Campo: "Beta-arrestin 1 is involved in the catabolic response stimulated by hyaluronan degradation in mouse chondrocytes." in: Cell and tissue research, Vol. 361, Issue 2, pp. 567-79, (2015) (PubMed).

    Sakthivel, Guruvayoorappan: "Acacia ferruginea inhibits inflammation by regulating inflammatory iNOS and COX-2." in: Journal of immunotoxicology, Vol. 13, Issue 1, pp. 127-35, (2015) (PubMed).

    Shathish, Sakthivel, Guruvayoorappan: "Protective Effect of Solanum muricatum on Tumor Metastasis by Regulating Inflammatory Mediators and Nuclear Factor-Kappa B Subunits." in: Journal of environmental pathology, toxicology and oncology : official organ of the International Society for Environmental Toxicology and Cancer, Vol. 34, Issue 3, pp. 249-62, (2015) (PubMed).

    Kochi, Shimizu, Shirakami, Yoshimi, Kuramoto, Tanaka, Moriwaki: "Utility of Apc-mutant rats with a colitis-associated colon carcinogenesis model for chemoprevention studies." in: European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP), Vol. 24, Issue 3, pp. 180-7, (2015) (PubMed).

    V, C: "Protective effect of marine mangrove Rhizophora apiculata on acetic acid induced experimental colitis by regulating anti-oxidant enzymes, inflammatory mediators and nuclear factor-kappa B subunits." in: International immunopharmacology, Vol. 18, Issue 1, pp. 124-34, (2014) (PubMed).

    Shathish, Guruvayoorappan: "Decalepis hamiltonii inhibits tumor progression and metastasis by regulating the inflammatory mediators and nuclear factor ?B subunits." in: Integrative cancer therapies, Vol. 13, Issue 2, pp. 141-51, (2014) (PubMed).

    Kim, Koppula, Hong, Jeon, Kwon, Hwang, Park, Choi: "Regulation of microglia activity by glaucocalyxin-A: attenuation of lipopolysaccharide-stimulated neuroinflammation through NF-?B and p38 MAPK signaling pathways." in: PLoS ONE, Vol. 8, Issue 2, pp. e55792, (2013) (PubMed).

    Filip, Postescu, Bolfa, Catoi, Muresan, Clichici: "Inhibition of UVB-induced skin phototoxicity by a grape seed extract as modulator of nitrosative stress, ERK/NF-kB signaling pathway and apoptosis, in SKH-1 mice." in: Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, Vol. 57, pp. 296-306, (2013) (PubMed).

    Campo, Avenoso, DAscola, Scuruchi, Prestipino, Calatroni, Campo: "Hyaluronan in part mediates IL-1beta-induced inflammation in mouse chondrocytes by up-regulating CD44 receptors." in: Gene, Vol. 494, Issue 1, pp. 24-35, (2012) (PubMed).

    Campo, Avenoso, DAscola, Scuruchi, Prestipino, Nastasi, Calatroni, Campo: "The inhibition of hyaluronan degradation reduced pro-inflammatory cytokines in mouse synovial fibroblasts subjected to collagen-induced arthritis." in: Journal of cellular biochemistry, Vol. 113, Issue 6, pp. 1852-67, (2012) (PubMed).

    Campo, Avenoso, DAscola, Scuruchi, Prestipino, Nastasi, Calatroni, Campo: "Adenosine A2A receptor activation and hyaluronan fragment inhibition reduce inflammation in mouse articular chondrocytes stimulated with interleukin-1?." in: The FEBS journal, Vol. 279, Issue 12, pp. 2120-33, (2012) (PubMed).

    Campo, Avenoso, Nastasi, Micali, Prestipino, Vaccaro, DAscola, Calatroni, Campo: "Hyaluronan reduces inflammation in experimental arthritis by modulating TLR-2 and TLR-4 cartilage expression." in: Biochimica et biophysica acta, Vol. 1812, Issue 9, pp. 1170-81, (2011) (PubMed).

    Campo, Avenoso, Micali, Nastasi, Squadrito, Altavilla, Bitto, Polito, Rinaldi, Calatroni, DAscola, Campo: "High-molecular weight hyaluronan reduced renal PKC activation in genetically diabetic mice." in: Biochimica et biophysica acta, Vol. 1802, Issue 11, pp. 1118-30, (2010) (PubMed).

    Ounsted, Moar: "Proportionality changes in the first year of life; the influence of weight for gestational age at birth." in: Acta paediatrica Scandinavica, Vol. 75, Issue 5, pp. 811-8, (1987) (PubMed).

  • Target See all NOS2 ELISA Kits
    NOS2 (Nitric Oxide Synthase 2, Inducible (NOS2))
    Abstract
    NOS2 Products
    Synonyms
    HEP-NOS ELISA Kit, INOS ELISA Kit, NOS ELISA Kit, NOS2A ELISA Kit, NOS-II ELISA Kit, Nos-2 ELISA Kit, Nos2a ELISA Kit, i-NOS ELISA Kit, iNOS ELISA Kit, iNos ELISA Kit, NOS2a ELISA Kit, NOS2 ELISA Kit, BmNOS2 ELISA Kit, Nsl ELISA Kit, nos2 ELISA Kit, nitric oxide synthase 2 ELISA Kit, nitric oxide synthase 2, inducible ELISA Kit, inducible nitric oxide synthase ELISA Kit, inducible nitric-oxide synthase ELISA Kit, nanos C2HC-type zinc finger 2 ELISA Kit, NOS2 ELISA Kit, Nos2 ELISA Kit, nos2 ELISA Kit, LOC396821 ELISA Kit, NANOS2 ELISA Kit
    UniProt
    P29477
    Pathways
    Retinoic Acid Receptor Signaling Pathway, Cellular Response to Molecule of Bacterial Origin, Inositol Metabolic Process, Regulation of Leukocyte Mediated Immunity, Positive Regulation of Immune Effector Process
You are here:
Support