HMOX1 ELISA Kit
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- Target Alle HMOX1 ELISA Kits anzeigen
- HMOX1 (Heme Oxygenase (Decycling) 1 (HMOX1))
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Reaktivität
- Ratte
- Nachweismethode
- Colorimetric
- Methodentyp
- Sandwich ELISA
- Detektionsbereich
- 0.15 ng/mL - 10 ng/mL
- Untere Nachweisgrenze
- 0.15 ng/mL
- Applikation
- ELISA
- Verwendungszweck
- The kit is a sandwich enzyme immunoassay for in vitro quantitative measurement of HO1 in rat serum, plasma, tissue homogenates.
- Proben
- Plasma, Serum, Tissue Homogenate
- Analytische Methode
- Quantitative
- Spezifität
- This assay has high sensitivity and excellent specificity for detection of Heme Oxygenase 1 (HO1)
- Sensitivität
- 0.065 ng/mL
- Bestandteile
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- 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
- Top Product
- Discover our top product HMOX1 ELISA Kit
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- Kommentare
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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. - Probenmenge
- 100 μL
- Testdauer
- 3 h
- Plattentyp
- Pre-coated
- Protokoll
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- Prepare all reagents, samples and standards,
- Add 100μL standard or sample to each well. Incubate 1 hours at 37 °C,
- Aspirate and add 100μL prepared Detection Reagent A. Incubate 1 hour at 37 °C,
- Aspirate and wash 3 times,
- Add 100μL prepared Detection Reagent B. Incubate 30 minutes at 37 °C,
- Aspirate and wash 5 times,
- Add 90μL Substrate Solution. Incubate 10-20 minutes at 37 °C,
- Add 50μL Stop Solution. Read at 450nm immediately.
- Aufbereitung der Reagenzien
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- Bring all kit components and samples to room temperature (18-25 °C) before use.
- 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 10 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 10 ng/mL, 5 ng/mL, 2.5 ng/mL, 1.25 ng/mL, 0.625 ng/mL, 0.312 ng/mL, 0.156 ng/mL, and the last microcentrifuge tube with Standard Diluent is the blank as 0 ng/mL.
- Detection Reagent A and Detection Reagent B - Briefly spin or centrifuge the stock Detection A and Detection B before use. Dilute to the working concentration with Assay Diluent A and B, respectively (1:100).
- 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).
- TMB substrate - Aspirate the needed dosage of the solution with sterilized tips and do not dump the residual solution into the vial again.
Note:
- Making serial dilution in the wells directly is not permitted.
- Prepare standard within 15 minutes before assay. Please do not dissolve the reagents at 37 °C directly.
- 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 once pipetting.
- The reconstituted Standards, Detection Reagent A and Detection Reagent B can be used only once.
- If crystals have formed in the Wash Solution concentrate (30x), warm to room temperature and mix gently until the crystals are completely dissolved.
- Contaminated water or container for reagent preparation will influence the detection result.
- Aufbereitung der Proben
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- 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).
- Testpräzision
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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% - Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Vorsichtsmaßnahmen
- The Stop Solution suggested for use with this kit is an acid solution. Wear eye, hand, face, and clothing protection when using this material.
- Lagerung
- 4 °C/-20 °C
- Informationen zur Lagerung
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- 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.
- 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.
- Haltbarkeit
- 6 months
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Quercetin and tin protoporphyrin attenuate hepatic ischemia reperfusion injury: role of HO-1." in: Naunyn-Schmiedeberg's archives of pharmacology, Vol. 390, Issue 9, pp. 871-881, (2018) (PubMed).
: "Ameliorative potential of sitagliptin and/or resveratrol on experimentally-induced clear cell renal cell carcinoma." in: Biomedicine & pharmacotherapy, Vol. 97, pp. 667-674, (2018) (PubMed).
: "Implication of Nrf2/HO-1 pathway in the coloprotective effect of coenzyme Q10 against experimentally induced ulcerative colitis." in: Inflammopharmacology, Vol. 25, Issue 1, pp. 119-135, (2017) (PubMed).
: "Sulforaphane protects against sodium valproate-induced acute liver injury." in: Canadian journal of physiology and pharmacology, Vol. 95, Issue 4, pp. 420-426, (2017) (PubMed).
: "Ellagic acid exerts protective effect in intrastriatal 6-hydroxydopamine rat model of Parkinson's disease: Possible involvement of ERβ/Nrf2/HO-1 signaling." in: Brain research, Vol. 1662, pp. 23-30, (2017) (PubMed).
: "Citrus leaf extract reduces blood pressure and vascular damage in repeatedly heated palm oil diet-Induced hypertensive rats." in: Biomedicine & pharmacotherapy, Vol. 87, pp. 451-460, (2017) (PubMed).
: "Berberine ameliorates intrahippocampal kainate-induced status epilepticus and consequent epileptogenic process in the rat: Underlying mechanisms." in: Biomedicine & pharmacotherapy, Vol. 87, pp. 200-208, (2017) (PubMed).
: "Carnosine ameliorates cognitive deficits in streptozotocin-induced diabetic rats: Possible involved mechanisms." in: Peptides, Vol. 86, pp. 102-111, (2016) (PubMed).
: "S-allyl cysteine ameliorates cognitive deficits in streptozotocin-diabetic rats via suppression of oxidative stress, inflammation, and acetylcholinesterase." in: European journal of pharmacology, Vol. 794, pp. 69-76, (2016) (PubMed).
: "
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Quercetin and tin protoporphyrin attenuate hepatic ischemia reperfusion injury: role of HO-1." in: Naunyn-Schmiedeberg's archives of pharmacology, Vol. 390, Issue 9, pp. 871-881, (2018) (PubMed).
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- Target Alle HMOX1 ELISA Kits anzeigen
- HMOX1 (Heme Oxygenase (Decycling) 1 (HMOX1))
- Andere Bezeichnung
- Heme Oxygenase 1 (HO1) (HMOX1 Produkte)
- Synonyme
- HMOX1 ELISA Kit, ARABIDOPSIS THALIANA HEME OXYGENASE 1 ELISA Kit, ATHO1 ELISA Kit, F18A8.4 ELISA Kit, F18A8_4 ELISA Kit, GENOMES UNCOUPLED 2 ELISA Kit, GUN2 ELISA Kit, HEME OXYGENASE ELISA Kit, HEME OXYGENASE 1 ELISA Kit, HEME OXYGENASE 6 ELISA Kit, HO1 ELISA Kit, HY1 ELISA Kit, HY6 ELISA Kit, PLASTID HEME OXYGENASE ELISA Kit, REVERSAL OF THE DET PHENOTYPE 4 ELISA Kit, HO-1 ELISA Kit, wu:fc27c04 ELISA Kit, zgc:65984 ELISA Kit, D8Wsu38e ELISA Kit, Hemox ELISA Kit, Hmox ELISA Kit, Hsp32 ELISA Kit, HEOXG ELISA Kit, Heox ELISA Kit, Ho-1 ELISA Kit, Ho1 ELISA Kit, hsp32 ELISA Kit, MGC132176 ELISA Kit, Hmox1 ELISA Kit, HMOX1D ELISA Kit, HSP32 ELISA Kit, bK286B10 ELISA Kit, heme oxygenase 1 ELISA Kit, Plant heme oxygenase (decyclizing) family protein ELISA Kit, Heme oxygenase ELISA Kit, heme oxygenase ELISA Kit, heme oxygenase 1, chloroplastic ELISA Kit, heme oxygenase 1a ELISA Kit, heme oxygenase 1 L homeolog ELISA Kit, HMOX1 ELISA Kit, TED4 ELISA Kit, ho1 ELISA Kit, P9301_RS17555 ELISA Kit, A9601_RS17590 ELISA Kit, MAE_RS06565 ELISA Kit, HO1 ELISA Kit, hmox1a ELISA Kit, CPE0214 ELISA Kit, Cyan7425_2962 ELISA Kit, Hmox1 ELISA Kit, hmox1.L ELISA Kit, AM1_C0205 ELISA Kit, CC1G_11686 ELISA Kit, CpipJ_CPIJ007246 ELISA Kit
- Pathways
- Transition Metal Ion Homeostasis, Regulation of Leukocyte Mediated Immunity, Positive Regulation of Immune Effector Process, Production of Molecular Mediator of Immune Response, SARS-CoV-2 Protein Interaktom
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