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SKU:SEA154Hu

ELISA Kit for Carbohydrate Antigen 125 (CA125)

ELISA Kit for Carbohydrate Antigen 125 (CA125)

Regular price $630.00 USD
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UOM
Sensitivity
Detection range

Enzyme-linked immunosorbent assay for Antigen Detection.

Product No.

SEA154Hu

Organism Species

Homo sapiens (Human).

Sample Type

Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids

Test Method

Double-antibody Sandwich

Assay Length

3h

Detection Range

1.56-100U/mL

Sensitivity

The minimum detectable dose of this kit is typically less than 0.58U/mL.

UOM

48T 96T 96T*5 96T*10 96T*100

Specificity

This assay has high sensitivity and excellent specificity for detection of Carbohydrate Antigen 125 (CA125).
No significant cross-reactivity or interference between Carbohydrate Antigen 125 (CA125) and analogues was observed.

Recovery

Matrices listed below were spiked with certain level of recombinant Carbohydrate Antigen 125 (CA125) and the recovery rates were calculated by comparing the measured value to the expected amount of Carbohydrate Antigen 125 (CA125) in samples.

Matrix Recovery range (%) Average(%)
serum(n=5) 78-94 90
EDTA plasma(n=5) 79-94 83
heparin plasma(n=5) 85-97 93

Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Carbohydrate Antigen 125 (CA125) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Carbohydrate Antigen 125 (CA125) 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 Carbohydrate Antigen 125 (CA125) 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) 92-101% 80-101% 79-97% 80-90%
EDTA plasma(n=5) 92-103% 98-105% 85-94% 95-102%
heparin plasma(n=5) 80-94% 79-104% 84-92% 94-101%

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.

Magazine Citations
PLoS One Selective Blocking of TNF Receptor 1 Attenuates Peritoneal Dialysis Fluid Induced Inflammation of the Peritoneum in Mice. pubmed:27755542
Tumor Biology KPNA2 is a potential diagnostic serum biomarker for epithelial ovarian cancer and correlates with poor prognosis pubmed:28651492
Oncotarget Diagnostic value of HE4+ circulating tumor cells in patients with suspicious ovarian cancer Pubmed:29484129
Prognostic value of STC1 expression in ovarian cancer
American Journal of Translational Research Synergistic effect of Tripterygium glycosides and cisplatin on drug-resistant human epithelial ovarian cancer via ILK/GSK3β/Slug signal pathway Pubmed:35422913
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