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HMGB1 ELISA 试剂盒

This Colorimetric ELISA kit is designed for the quantitative measurement of 小鼠 HMGB1. There are 30 publications available.
产品编号 ABIN415379
发货至: 中国
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Quick Overview for HMGB1 ELISA 试剂盒 (ABIN415379)

抗原

See all HMGB1 ELISA试剂盒
HMGB1 (High Mobility Group Box 1 (HMGB1))

适用

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小鼠

检测方法

Colorimetric

实验类型

Sandwich ELISA

检测范围

46.88 pg/mL - 3000 pg/mL

应用范围

ELISA

样品类型

Plasma, Serum
  • 最低检测浓度

    46.88 pg/mL

    原理

    The kit is a sandwich enzyme immunoassay for in vitro quantitative measurement of HMG1 in mouse serum, plasma.

    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.

    Analytical Method

    Quantitative

    特异性

    This assay has high sensitivity and excellent specificity for detection of High Mobility Group Protein 1 (HMGB1).
    No significant cross-reactivity or interference between High Mobility Group Protein 1 (HMGB1) and analogues was observed.

    交叉反应 (详细)

    No significant cross-reactivity or interference between High Mobility Group Protein 1 (HMG1) and analogues was observed.

    灵敏度

    < 18.29 pg/mL

    组件

    • Pre-coated, 96-well strip plate
    • Plate sealer
    • Standard
    • Standard Diluent
    • Detection Reagent A
    • Assay Diluent A
    • Detection Reagent B
    • Assay Diluent B
    • TMB Substrate
    • Stop Solution
    • Wash Buffer (30X)
    • Instruction manual

    试剂未包括

    • Microplate reader with 450 nm filter.
    • Precision single or multi-channel pipettes and disposable tips.
    • Eppendorf Tubes for diluting samples.
    • Deionized or distilled water.
    • Absorbent paper for blotting the microtiter plate.
    • Container for Wash Solution
  • 应用备注

    • Limited by the current condition and scientific technology, we cannot completely conduct the comprehensive identification and analysis on the raw material provided by suppliers. So there might be some qualitative and technical risks to use the kit.
    • The final experimental results will be closely related to validity of the products, operation skills of the end users and the experimental environments. Please make sure that sufficient samples are available.
    • Kits from different batches may be a little different in detection range, sensitivity and color developing time.
    • Do not mix or substitute reagents from one kit lot to another. Use only the reagents supplied by manufacturer.
    • Protect all reagents from strong light during storage and incubation. All the bottle caps of reagents should be covered tightly to prevent the evaporation and contamination of microorganism.
    • There may be some foggy substance in the wells when the plate is opened at the first time. It will not have any effect on the final assay results. Do not remove microtiter plate from the storage bag until needed.
    • Wrong operations during the reagents preparation and loading, as well as incorrect parameter setting for the plate reader may lead to incorrect results. A microplate plate reader with a bandwidth of 10nm or less and an optical density range of 0-3 O.D. or greater at 450 ± 10nm wavelength is acceptable for use in absorbance measurement. Please read the instruction carefully and adjust the instrument prior to the experiment.
    • Even the same operator might get different results in two separate experiments. In order to get better reproducible results, the operation of every step in the assay should be controlled. Furthermore, a preliminary experiment before assay for each batch is recommended.
    • Each kit has been strictly passed Q.C test. However, results from end users might be inconsistent with our in-house data due to some unexpected transportation conditions or different lab equipments. Intra-assay variance among kits from different batches might arise from above factors, too.
    • Kits from different manufacturers for the same item might produce different results, since we have not compared our products with other manufacturers.

    说明

    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.

    样本量

    100 μL

    实验时间

    3 h

    板类型

    Pre-coated

    实验流程

    1. Prepare all reagents, samples and standards;
    2. Add 100µL standard or sample to each well. Incubate 2 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.

    实验精密度

    Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level High Mobility Group Protein 1 (HMGB1) were tested 20 times on one plate, respectively.
    Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level High Mobility Group Protein 1 (HMGB1) were tested on 3 different plates, 8 replicates in each plate.
    CV(%) = SD/meanX100
    Intra-Assay: CV<10%
    Inter-Assay: CV<12%

    限制

    仅限研究用
  • 注意事项

    The Stop Solution suggested for use with this kit is an acid solution. Wear eye, hand, face, and clothing protection when using this material.

    注意事项

    The stability of 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 condition.
    To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.

    储存条件

    4 °C

    储存方法

    • For unopened kit: All the reagents should be kept according to the labels on vials. The Standard, Detection Reagent A, Detection Reagent B and the 96-well strip plate should be stored at -20°C upon receipt while the others should be at 4°C.
    • For opened kit: When the kit is opened, the remaining reagents still 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 reseal along entire edge of zip-seal.
      Note: It is highly recommended to use the remaining reagents within 1 month provided this is within the expiration date of the kit.
    • For ELISA kit, 1 day storage at 37°C can be considered as 2 months at 4°C, which means 3 days at 37°C equaling 6 months at 4°C.

    有效期

    6 months
  • Wang, Zhou, Wang, Sun: "Suppression of high-mobility group box 1 ameliorates xerostomia in a Sjögren syndrome-triggered mouse model." in: Canadian journal of physiology and pharmacology, Vol. 98, Issue 6, pp. 351-356, (2021) (PubMed).

    Hanson, Hernady, Reed, Johnston, Groves, Finkelstein: "Apoptosis Resistance in Fibroblasts Precedes Progressive Scarring in Pulmonary Fibrosis and Is Partially Mediated by Toll-Like Receptor 4 Activation." in: Toxicological sciences : an official journal of the Society of Toxicology, Vol. 170, Issue 2, pp. 489-498, (2020) (PubMed).

    Kawahara, Goto, Kodama, Luo, Fujiwara-Tani, Mori, Miyagawa, Tanaka, Kodama, Hosoito, Taniguchi, Kuniyasu: "Magnetic Hyperthermia Using Self-Controlled Heating Elements Consisting of Fe-Al Milling Alloy Induces Cancer Cell Apoptosis while Preserving Skeletal Muscle." in: Pathobiology : journal of immunopathology, molecular and cellular biology, Vol. 86, Issue 5-6, pp. 254-262, (2020) (PubMed).

    Adamiak, Cymer, Anusz, Tracz, Ratajczak: "A Novel Evidence That Mannan Binding Lectin (MBL) Pathway of Complement Cascade Activation is Involved in Homing and Engraftment of Hematopoietic Stem Progenitor Cells (HSPCs)." in: Stem cell reviews and reports, Vol. 16, Issue 4, pp. 693-701, (2020) (PubMed).

    Yu, Shi, Yu, Liu, Li, Liu, Wang, Chen: "Inhibition of calpain alleviates coxsackievirus B3-induced myocarditis through suppressing the canonical NLRP3 inflammasome/caspase-1-mediated and noncanonical caspase-11-mediated pyroptosis pathways." in: American journal of translational research, Vol. 12, Issue 5, pp. 1954-1964, (2020) (PubMed).

    Linders, Madhi, Rahman, Mörgelin, Regner, Brenner, Wang, Thorlacius: "Extracellular cold-inducible RNA-binding protein regulates neutrophil extracellular trap formation and tissue damage in acute pancreatitis." in: Laboratory investigation; a journal of technical methods and pathology, Vol. 100, Issue 12, pp. 1618-1630, (2020) (PubMed).

    Lee, Wang, Li, Liu: "Anti-inflammatory effect of cinnamaldehyde and linalool from the leaf essential oil of Cinnamomum osmophloeum Kanehira in endotoxin-induced mice." in: Journal of food and drug analysis, Vol. 26, Issue 1, pp. 211-220, (2019) (PubMed).

    Park, Kim, Kim, Chang: "Luteolin activates ERK1/2- and Ca2+-dependent HO-1 induction that reduces LPS-induced HMGB1, iNOS/NO, and COX-2 expression in RAW264.7 cells and mitigates acute lung injury of endotoxin mice." in: Inflammation research : official journal of the European Histamine Research Society ... [et al.], Vol. 67, Issue 5, pp. 445-453, (2018) (PubMed).

    Kim, Park, Kim, Chang: "Sirt1 S-nitrosylation induces acetylation of HMGB1 in LPS-activated RAW264.7 cells and endotoxemic mice." in: Biochemical and biophysical research communications, Vol. 501, Issue 1, pp. 73-79, (2018) (PubMed).

    Wang, Li, Deng, Liu, He: "Ursolic Acid Ameliorates Inflammation in Cerebral Ischemia and Reperfusion Injury Possibly via High Mobility Group Box 1/Toll-Like Receptor 4/NFκB Pathway." in: Frontiers in neurology, Vol. 9, pp. 253, (2018) (PubMed).

    Qian, Wei, Xu, He, Hua, Li, Hu, Lin, Gong, Meng, Zhou, Teng, Song: "Bone marrow-derived mesenchymal stem cells (BMSCs) repair acute necrotized pancreatitis by secreting microRNA-9 to target the NF-κB1/p50 gene in rats." in: Scientific reports, Vol. 7, Issue 1, pp. 581, (2017) (PubMed).

    Chen, Fang, Li, Chen, Li, Gong, Fang: "Glycyrrhizin ameliorates experimental colitis through attenuating interleukin-17-producing T cell responses via regulating antigen-presenting cells." in: Immunologic research, Vol. 65, Issue 3, pp. 666-680, (2017) (PubMed).

    Chaochao, Lou, Yang, Liu, Hu, Min, Chen, He, Chen: "Macrophage Inflammatory Protein-2 in High Mobility Group Box 1 Secretion of Macrophage Cells Exposed to Lipopolysaccharide." in: Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, Vol. 42, Issue 3, pp. 913-928, (2017) (PubMed).

    Peng, Liu, Ojcius, Lee, Chen, Huang, Martel, Young: "Mineral particles stimulate innate immunity through neutrophil extracellular traps containing HMGB1." in: Scientific reports, Vol. 7, Issue 1, pp. 16628, (2017) (PubMed).

    Yadav, Rani, Deep, Singh, Palle: "Oxidative Stress in Metabolic Disorders: Pathogenesis, Prevention, and Therapeutics." in: Oxidative medicine and cellular longevity, Vol. 2016, pp. 9137629, (2016) (PubMed).

    Yu, Yu, Liu, Yu, Liu, Liu, Su, Jiang, Chen: "Ethyl pyruvate attenuated coxsackievirus B3-induced acute viral myocarditis by suppression of HMGB1/RAGE/NF-ΚB pathway." in: SpringerPlus, Vol. 5, pp. 215, (2016) (PubMed).

    Kopecka, Porto, Lusa, Gazzano, Salzano, Pinzòn-Daza, Giordano, Desiderio, Ghigo, De Rosa, Caraglia, Riganti: "Zoledronic acid-encapsulating self-assembling nanoparticles and doxorubicin: a combinatorial approach to overcome simultaneously chemoresistance and immunoresistance in breast tumors." in: Oncotarget, Vol. 7, Issue 15, pp. 20753-72, (2016) (PubMed).

    Liu, Ma, Sun, Li, Wang: "High Mobility Group Box1 Protein Is Involved in Endoplasmic Reticulum Stress Induced by Clostridium difficile Toxin A." in: BioMed research international, Vol. 2016, pp. 4130834, (2016) (PubMed).

    Chen, Li, Khan, Shi, Wang, Zheng, Gong, Fang: "HMGB1 exacerbates experimental mouse colitis by enhancing innate lymphoid cells 3 inflammatory responses via promoted IL-23 production." in: Innate immunity, Vol. 22, Issue 8, pp. 696-705, (2016) (PubMed).

    Wu, Sheng, Xie, Li, Chen, Li, Wang, Xu: "Reduced HMGB 1-Mediated Pathway and Oxidative Stress in Resveratrol-Treated Diabetic Mice: A Possible Mechanism of Cardioprotection of Resveratrol in Diabetes Mellitus." in: Oxidative medicine and cellular longevity, Vol. 2016, pp. 9836860, (2016) (PubMed).

  • 抗原 See all HMGB1 ELISA试剂盒

    HMGB1 (High Mobility Group Box 1 (HMGB1))

    别名

    HMG1

    背景

    HMG1, HMG3, SBP1, Sulfoglucuronyl Carbohydrate Binding Protein, Amphoterin, High Mobility Group Box 1 Protein

    UniProt

    P63158

    途径

    p53 Pathway, Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development, Positive Regulation of Endopeptidase Activity, Regulation of Carbohydrate Metabolic Process, Toll-Like Receptors Cascades, Smooth Muscle Cell Migration, Inflammasome
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