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ELISA Kit for Guanylate Cyclase Activator 2B (GUCA2B)

UGN; GCAP-II; Uroguanylin; Guanylate cyclase C-activating peptide II

Specificity

This assay has high sensitivity and excellent specificity for detection of Guanylate Cyclase Activator 2B (GUCA2B).
No significant cross-reactivity or interference between Guanylate Cyclase Activator 2B (GUCA2B) and analogues was observed.

Recovery

Matrices listed below were spiked with certain level of recombinant Guanylate Cyclase Activator 2B (GUCA2B) and the recovery rates were calculated by comparing the measured value to the expected amount of Guanylate Cyclase Activator 2B (GUCA2B) in samples.

Matrix Recovery range (%) Average(%)
serum(n=5) 97-104 101
EDTA plasma(n=5) 80-89 83
heparin plasma(n=5) 97-104 101

Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Guanylate Cyclase Activator 2B (GUCA2B) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Guanylate Cyclase Activator 2B (GUCA2B) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%

Linearity

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Guanylate Cyclase Activator 2B (GUCA2B) and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.

Sample 1:2 1:4 1:8 1:16
serum(n=5) 85-97% 92-101% 95-105% 89-104%
EDTA plasma(n=5) 82-97% 95-103% 93-101% 78-96%
heparin plasma(n=5) 96-103% 91-99% 78-101% 89-104%

Stability

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.

Reagents and materials provided

Reagents Quantity Reagents Quantity
Pre-coated, ready to use 96-well strip plate 1 Plate sealer for 96 wells 4
Standard 2 Standard Diluent 1×20mL
Detection Reagent A 1×120µL Assay Diluent A 1×12mL
Detection Reagent B 1×120µL Assay Diluent B 1×12mL
TMB Substrate 1×9mL Stop Solution 1×6mL
Wash Buffer (30 × concentrate) 1×20mL Instruction manual 1

Assay procedure summary

1. Prepare all reagents, samples and standards;
2. Add 100µL standard or sample to each well. Incubate 1 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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Magazine Citations
Int J Obes (Lond) Cavia (Guinea pig )anylin and uroCavia (Guinea pig )anylin stimulate lipolysis in human visceral adipocytes Pubmed:27108812
Metabolism Clinical and Experimental High plasma and lingual uroguanylin as potential contributors to changes in food preference after sleeve gastrectomy Pubmed:34990711
Catalog No. Related products for research use of Homo sapiens (Human) Organism species Applications (RESEARCH USE ONLY!)
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