PON1 ELISA 试剂盒
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北京 101111
Quick Overview for PON1 ELISA 试剂盒 (ABIN414651)
抗原
See all PON1 ELISA试剂盒适用
检测方法
实验类型
检测范围
应用范围
样品类型
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最低检测浓度
- 3.12 ng/mL
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原理
- The kit is a sandwich enzyme immunoassay for in vitro quantitative measurement of PON1 in Serum,Plasma,Biological Fluids
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Analytical Method
- Quantitative
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特异性
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This assay has high sensitivity and excellent specificity for detection of Paraoxonase 1 (PON1).
No significant cross-reactivity or interference between Paraoxonase 1 (PON1) and analogues was observed. -
交叉反应 (详细)
- No significant cross-reactivity or interference between Paraoxonase 1 (PON1) and analogues was observed.
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灵敏度
- < 1.21 ng/mL
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组件
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- 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
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试剂未包括
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- 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
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应用备注
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- 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.
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说明
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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
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实验时间
- 3 h
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板类型
- Pre-coated
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实验流程
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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.
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实验精密度
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Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Paraoxonase 1 (PON1) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Paraoxonase 1 (PON1) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%
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限制
- 仅限研究用
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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.
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注意事项
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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
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储存方法
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- 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.
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有效期
- 6 months
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: "PON-1 haplotype (-108C>T, L55M, and Q192R) modulates the serum levels and activity PONase promoting an atherogenic lipid profile in rheumatoid arthritis patients." in: Clinical rheumatology, Vol. 40, Issue 2, pp. 741-752, (2021) (PubMed).
: "Estimating renal and hepatic clearance rates of organophosphate esters in humans: Impacts of intrinsic metabolism and binding affinity with plasma proteins." in: Environment international, Vol. 134, pp. 105321, (2020) (PubMed).
: "The role of PON-1, GR, IL-18, and OxLDL in depression with and without posttraumatic stress disorder." in: Pharmacological reports : PR, Vol. 69, Issue 5, pp. 837-845, (2018) (PubMed).
: "Individuals with autism have higher 8-Iso-PGF2α levels than controls, but no correlation with quantitative assay of Paraoxonase 1 serum levels." in: Metabolic brain disease, Vol. 32, Issue 6, pp. 1943-1950, (2018) (PubMed).
: "A case-control study: The association of serum paraoxonase 1 activity and concentration with the development of type 2 diabetes mellitus." in: Diabetes/metabolism research and reviews, Vol. 34, Issue 3, (2018) (PubMed).
: "Paraoxonase-1 is a better indicator than HDL of Atherosclerosis - A pilot study in North Indian population." in: Diabetes & metabolic syndrome, Vol. 12, Issue 3, pp. 275-278, (2018) (PubMed).
: "Serum Endocan Levels are Associated With Paraoxonase 1 Concentration in Patients With Chronic Kidney Disease." in: Therapeutic apheresis and dialysis : official peer-reviewed journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy, Vol. 22, Issue 4, pp. 325-331, (2018) (PubMed).
: "Association of lipid profile with serum PON1 concentration in patients with chronic kidney disease." in: Renal failure, pp. 1-6, (2016) (PubMed).
: "Association of paraoxonase 1 (PON1) gene polymorphisms and concentration with essential hypertension." in: Clinical and experimental hypertension (New York, N.Y. : 1993), Vol. 38, Issue 7, pp. 602-607, (2016) (PubMed).
: "Sympathoadrenal activation and endothelial damage are inter correlated and predict increased mortality in patients resuscitated after out-of-hospital cardiac arrest. a post Hoc sub-study of patients ..." in: PLoS ONE, Vol. 10, Issue 3, pp. e0120914, (2015) (PubMed).
: "Paraoxonase responses to exercise and niacin therapy in men with metabolic syndrome." in: Redox report : communications in free radical research, Vol. 20, Issue 1, pp. 42-8, (2014) (PubMed).
: "Extra-virgin olive oil consumption reduces the age-related decrease in HDL and paraoxonase 1 anti-inflammatory activities." in: The British journal of nutrition, Vol. 110, Issue 7, pp. 1272-84, (2013) (PubMed).
: "Paraoxonase 1: a better atherosclerotic risk predictor than HDL in type 2 diabetes mellitus." in: Diabetes & metabolic syndrome, Vol. 7, Issue 2, pp. 108-11, (2013) (PubMed).
: "Combined serum proteomic and metabonomic profiling after laparoscopic sleeve gastrectomy in children and adolescents." in: Journal of laparoendoscopic & advanced surgical techniques. Part A, Vol. 22, Issue 2, pp. 184-8, (2012) (PubMed).
: "Beneficial effects of omega-3 fatty acids in the proteome of high-density lipoprotein proteome." in: Lipids in health and disease, Vol. 11, Issue 1, pp. 116, (2012) (PubMed).
: "Persistent elevation of paraoxonase-1 specific enzyme activity after weight reduction in obese non-diabetic men with metabolic syndrome." in: Clinica chimica acta; international journal of clinical chemistry, Vol. 412, Issue 19-20, pp. 1835-41, (2011) (PubMed).
: "High density lipoprotein structural changes and drug response in lipidomic profiles following the long-term fenofibrate therapy in the FIELD substudy." in: PLoS ONE, Vol. 6, Issue 8, pp. e23589, (2011) (PubMed).
: "Macrophage cholesterol efflux to plasma and HDL in subjects with low and high homocysteine levels: a FIELD substudy." in: Atherosclerosis, Vol. 219, Issue 1, pp. 259-65, (2011) (PubMed).
: "The anti-inflammatory and neuroprotective effects of ghrelin in subarachnoid hemorrhage-induced oxidative brain damage in rats." in: Journal of neurotrauma, Vol. 27, Issue 6, pp. 1143-55, (2010) (PubMed).
: "Immobilized arylsulfotransferase." in: Journal of biochemistry, Vol. 102, Issue 3, pp. 487-91, (1988) (PubMed).
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- PON1 (Paraoxonase 1 (PON1))
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别名
- PON1
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背景
- ESA, PON, Esterase A, Serum paraoxonase/arylesterase 1, Aromatic esterase 1, A-esterase 1, Serum aryldialkylphosphatase 1
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UniProt
- P27169
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