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APOE ELISA Kit

APOE Reactivity: Mouse Colorimetric Competition ELISA 6.25 ng/mL - 400 ng/mL Cell Culture Supernatant, Plasma, Serum, Tissue Homogenate
Catalog No. ABIN6975758
  • Target See all APOE ELISA Kits
    APOE (Apolipoprotein E (APOE))
    Reactivity
    • 7
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Mouse
    Detection Method
    Colorimetric
    Method Type
    Competition ELISA
    Detection Range
    6.25 ng/mL - 400 ng/mL
    Minimum Detection Limit
    6.25 ng/mL
    Application
    ELISA
    Purpose
    For the quantitative determination of mouse apolipoprotein E (Apo-E) concentrations in serum, plasma, tissue homogenates, cell culture supernates.
    Sample Type
    Cell Culture Supernatant, Plasma, Serum, Tissue Homogenate
    Analytical Method
    Quantitative
    Specificity
    This assay has high sensitivity and excellent specificity for detection of mouse Apo-E. No significant cross-reactivity or interference between mouse Apo-E and analogues was observed. Note: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between mouse Apo-E and all the analogues, therefore, cross reaction may still exist.
    Sensitivity
    1.56 ng/mL
    Components
    • Assay plate
    • Standard
    • HRP-conjugate (100 x concentrate)
    • Sample Diluent
    • HRP-conjugate Diluent
    • Wash Buffer (25 x concentrate)
    • TMB Substrate
    • Stop Solution
    • Adhesive Strip
  • Stop Solution
  • Adhesive Strip
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    Discover our top product APOE ELISA Kit
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Sample Volume
    50 μL
    Assay Time
    1 - 4.5 h
    Plate
    Pre-coated
    Protocol
    1. Prepare reagents, samples and standards as instructed.
    2. Set a Blank well without any solution.
    3. Add 50 µL standard or sample to each well.
    4. Add 50 µL HRP-conjugate (1x) to each well (Not to Blank well).
    5. Incubate 1 hour at 37 °C
    6. Aspirate and wash 5 times.
    7. Add 90 μL of TMB Substrate to each well. Incubate for 20 minutes at 37 °C. Protect from light.
    8. Add 50 µL Stop Solution to each well. Read at 450 nm within 5 minutes.
    Reagent Preparation
    1. HRP-conjugate (1x) - Centrifuge the vial before opening. HRP-conjugate requires a 100-fold dilution. A suggested 100-fold dilution is 10 μL of HRP-conjugate + 990 μL of HRP-conjugate Diluent.
    2. Wash Buffer(1x)- If crystals have formed in the concentrate, warm up to room temperature and mix gently until the crystals have completely dissolved. Dilute 20 mL of Wash Buffer Concentrate (25 x) into deionized or distilled water to prepare 500 mL of Wash Buffer (1 x).
    3. Standard Centrifuge the standard vial at 6000-10000rpm for 30s. Reconstitute the Standard with 1.0 mL of Sample Diluent. Do not substitute other diluents. This reconstitution produces a stock solution of 400 ng/mL. 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 150 μL of Sample Diluent into each tube (S0-S6). Use the stock solution to produce a 2-fold dilution series (below). Mix each tube thoroughly before the next transfer. The undiluted Standard serves as the high standard (400 ng/mL). Sample Diluent serves as the zero standard (0 ng/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, and 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 10 μL for once pipetting.
    • Distilled water is recommended to be used to make the preparation for reagents. 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).
    Note:
    Recommend to dilute the serum or plasma samples with Sample Diluent(1:500) before test. The suggested 500-fold dilution can be achieved by adding 5 μL sample to 95 μL of Sample Diluent first, then complete the 500-fold dilution by adding 10 μL of this solution to 240 μL of Sample Diluent. The recommended dilution factor is for reference only. The optimal di lution factor should be determined by users according to their particular experiments. 6
    Assay Precision
    Intra-assay Precision (Precision within an assay): CV%<8% Three samples of known concentration were tested twenty times on one plate to assess.
    Inter-assay Precision (Precision between assays): CV%<10% Three samples of known concentration were tested in twenty assays to assess.
    Restrictions
    For Research Use only
  • Storage
    4 °C,-20 °C
    Storage Comment
    Unopened kit Store at 2 - 8°C. Do not use the kit beyond the expiration date. May be stored for up to 1 month at 2 - 8°C. Coated assay Try to keep it in a sealed aluminum foil bag, plate and avoid the damp. Standard May be stored for up to 1 month at 2 - 8° C. If don't make recent use, better keep it store at HRP-conjugate -20°C. Opened kit HRP-conjugate Diluent Sample Diluent May be stored for up to 1 month at 2 - 8°C. Wash Buffer TMB Substrate Stop Solution *Provided this is within the expiration date of the kit.
    Expiry Date
    6 months
  • Wittenberg, Nassiri, Francuzik, Lehmann, Babina, Worm: "Serum levels of 9α,11β-PGF2 and apolipoprotein A1 achieve high predictive power as biomarkers of anaphylaxis." in: Allergy, (2017) (PubMed).

  • Target See all APOE ELISA Kits
    APOE (Apolipoprotein E (APOE))
    Alternative Name
    apolipoprotein E (APOE Products)
    Synonyms
    ad2 ELISA Kit, apoprotein ELISA Kit, im:7036787 ELISA Kit, wu:fb69a05 ELISA Kit, zgc:110064 ELISA Kit, apoe ELISA Kit, AI255918 ELISA Kit, AD2 ELISA Kit, LDLCQ5 ELISA Kit, LPG ELISA Kit, APOEA ELISA Kit, Apo-E ELISA Kit, apolipoprotein E ELISA Kit, apolipoprotein Ea ELISA Kit, apoe ELISA Kit, apoea ELISA Kit, Apoe ELISA Kit, APOE ELISA Kit
    Background

    Abbreviation: APOE

    Alias: AD2, LDLCQ5, LPG, MGC1571, apolipoprotein E3

    UniProt
    P08226
    Pathways
    Regulation of Cell Size, Lipid Metabolism
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