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HSD17B10 ELISA Kit

This Human HSD17B10 ELISA Kit is a Colorimetric ELISA Kit designed to quantify Human HSD17B10.
Catalog No. ABIN2944789

Quick Overview for HSD17B10 ELISA Kit (ABIN2944789)

Target

See all HSD17B10 ELISA Kits
HSD17B10 (Hydroxysteroid (17-Beta) Dehydrogenase 10 (HSD17B10))

Reactivity

  • 3
  • 2
  • 2
  • 1
Human

Detection Method

Colorimetric

Method Type

Sandwich ELISA

Detection Range

25 pg/mL - 1600 pg/mL

Application

ELISA

Sample Type

Plasma, Serum
  • Minimum Detection Limit

    25 pg/mL

    Purpose

    Human 17-Beta-Hydroxysteroid Dehydrogenase Type 10 (HSD17B10) ELISA Kit

    Analytical Method

    Quantitative

    Sensitivity

    15 pg/mL

    Components

    The kit components listed are for reference only. The product manual may differ slightly. The product should be used as stated on the product manual included and delivered together with the product.
    • Pre-coated 96-Well Microplate
    • Standard
    • Standard Diluent Buffer
    • Wash Buffer
    • Detection Reagent A
    • Detection Reagent B
    • Diluent A
    • Diluent B
    • TMB Substrate
    • Stop Solution
    • Plate Sealer

    Material not included

    • 37 °C incubator
    • Multi and single channel pipettes and sterile pipette tips
    • Squirt bottle or automated microplate washer
    • 1.5 mL tubes
    • Distilled water
    • Absorbent filter papers
    • 100 mL and 1 liter graduated cylinders
    • Microplate reader (wavelength: 450 nm)
    • ELISA Shaker
  • Application Notes

    Optimal dilutions/concentrations should be determined by the end user.

    Comment

    The stability of the kit is determined by the rate of activity loss. The loss rate is less than 5 % within the expiration date under appropriate storage conditions. To minimize performance fluctuations, operation procedures and lab conditions should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same user throughout.

    Sample Volume

    100 µL

    Plate

    Pre-coated

    Reagent Preparation

    This procedure is provided for reference only. The product manual may differ slightly. The product should be used as stated on the product manual included and delivered together with the product.

    • 1) Standard: Prepare the standard with the recommended volume of Standard Diluent Buffer, to make the standard solution. Then use the Standard Diluent buffer to carry out serial dilutions of the standard solution, as instructed in the Protocol.
    • 2) Wash Buffer: Dilute the concentrated Wash Buffer with distilled water, as instructed in the Protocol.
    • 3) Detection Reagent Preparation: Calculate the total volume of working solution required. Dilute Detection Reagent A and Detection Reagent B with Diluent A and Diluent B, respectively, at 1:100.

    Assay Procedure

    This procedure is provided for reference only. The product manual may differ slightly. The product should be used as stated on the product manual included and delivered together with the product.

    • Equilibrate the kit components and samples to room temperature (18 - 25 °C) before use. It is recommended to plot a standard curve for each test.
    • 1. Set standard, test sample and control (zero) wells on the pre-coated plate respectively, and then, record their positions. It is recommended to measure each standard and sample at least in duplicate.
    • 2. Add 100 μL of each standard, control and sample into the appropriate wells. Seal the plate with a cover and incubate for 1 h at 37 °C.
    • 3. Remove the cover and discard the liquid.
    • 4. Add 100 μL of the detection Reagent A working solution to each well. Seal the plate with a cover and incubate for 1 h at 37 °C.
    • 5. Remove the cover and discard the solution. Wash the plate 3 times with 1X Wash Buffer.
    • 6. Add 100 μL of Detection Reagent B working solution into each well, seal and incubate at 37 °C for 30 min.
    • 7. Discard the solution and wash the plate 5 times with wash buffer as explained in previous step.
    • 8. Aliquot 90 μL of TMB Substrate into each well. Seal the plate with a cover and incubate at 37 °C for 10-20 min. Avoid exposure to light. The incubation time is for reference use only, the optimal time should be determined by end user. Do not exceed 30 min.
    • 9. Add 50 μL of Stop Solution to each well. Read at 450 nm immediately.

    Calculation of Results

    For calculation, average the O.D.450 duplicate readings for each reference standard and each sample and substract the average control (zero) O.D.450 reading. The standard curve can be plotted as the relative O.D.450 of each reference standard solution (Y) vs. the respective concentration of each standard solution (X). The HSD17B10 concentration of the samples can be interpolated from the standard curve.

    Assay Precision

    Intra-assay Precision (Precision within an assay): 3 samples with low, medium and high levels of 17-Beta-Hydroxysteroid Dehydrogenase Type 10 (HSD17B10) were tested 20 times on one plate, respectively.

    Inter-assay Precision (Precision between assays): 3 samples with low, medium and high levels of 17-Beta-Hydroxysteroid Dehydrogenase Type 10 (HSD17B10) were tested on 3 different plates, 8 replicates in each plate.

    CV (%) = (Standard Deviation / mean) x 100

    Intra-Assay: CV<10%

    Inter-Assay: CV<10%

    Restrictions

    For Research Use only
  • Storage

    4 °C

    Storage Comment

    Shipped at 4 °C. Upon receipt, store the kit according to the storage instruction in the kit's manual.

    Expiry Date

    6 months
  • Target See all HSD17B10 ELISA Kits

    HSD17B10 (Hydroxysteroid (17-Beta) Dehydrogenase 10 (HSD17B10))

    Alternative Name

    17-Beta-Hydroxysteroid Dehydrogenase Type 10

    Background

    HCD2_HUMAN

    Gene ID

    3028

    HGNC

    4800

    OMIM

    300256

    UniProt

    Q99714
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