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Mirikizumab ELISA Kit

Catalog #:   KDJ63101 Specific References (0) DATASHEET
Applications: Used for the quantitative determination of Mirikizumab concentration in serum and plasma.
Sample type: Plasma, Serum
Sensitivity: 78.23 ng/mL
Range: 234.38 - 15,000 ng/mL
Overview

Catalog No.

KDJ63101

Description

PRINCIPLE OF THE ASSAY This assay employs the quantitative competitive enzyme immunoassay technique. Recombinant Human IL23A has been pre-coated onto a microplate. Standards or samples are premixed with biotin-labeled antibody and then pipetted into the wells. Mirikizumab in the sample competitively binds to the pre-coated protein with biotin-labeled Mirikizumab. After washing away any unbound substances, Streptavidin-HRP is added to the wells. Following a wash to remove any unbound enzyme reagent, a substrate solution is added to the wells and color develops in inversely proportion to the amount of Mirikizumab bound in the initial step. The color development is stopped and the intensity of the color is measured.

Applications

Used for the quantitative determination of Mirikizumab concentration in serum and plasma.

Detection method

Colorimetric

Sample type

Plasma, Serum

Assay type

Quantitative

Range

234.38 - 15,000 ng/mL

Sensitivity

78.23 ng/mL

Precision

Intra-Assay Precision (Precision within an assay): <20%

Three samples of known concentration were tested sixteen times on one plate to assess intra-assay precision.

Inter-Assay Precision (Precision between assays): <20%

Three samples of known concentration were tested in twenty four separate assays to assess inter-assay precision.

 

Intra-Assay Precision

Inter-Assay Precision

Sample

1

2

3

1

2

3

n

16

16

16

24

24

24

Mean (ng/mL)

8257.1

1990.4

471.8

7736.7

1743.9

431.3

Standard deviation

596.3

148.3

35.6

907.0

207.7

52.2

CV (%)

7.2

7.5

7.5

11.7

11.9

12.1

 

Recovery

80-120%

Shipping

2-8 ℃

Stability and Storage

The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 10% prior to the expiration date under appropriate storage condition.

Alternative Names

LY-3074828, CAS: 1884201-71-1

Background

Mirikizumab (Eli Lilly and Company), Risankizumab (Boehringer Ingelheim and AbbVie), Tildrakizumab (Sun Pharma), Brazikumab (AstraZeneca), and Guselkumab (Janssen Biotech Inc.) are other drugs which target IL-23 and received the FDA approval for the treatment of psoriasis.

Data Image
  • Experiment Example
    CALCULATION OF RESULTS
    Average the duplicate readings for each standard and sample. Construct a standard curve by plotting the mean absorbance for each standard on the Y-axis against the concentration on the X-axis and draw a best fit curve through the points on the graph. Do not include the blank in the standard curve. The data may be linearized by plotting the log of the Mirikizumab concentrations versus the log of the O.D. and the best fit line can be determined by regression analysis. This procedure will produce an adequate but less precise fit of the data. If samples have been diluted, the concentration read from the standard curve must be multiplied by the dilution factor.
References
Datasheet

Document Download

Mirikizumab ELISA Kit.pdf

 

$ 1128
Product specifications
96 T 1128

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For research use only. Not for human or drug use.

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Mirikizumab ELISA Kit [KDJ63101]
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