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Quick Details

Place of Origin: United States
Brand Name: CBIOS or Perfemed
Type: Visual Acuity Examination Apparatus

Specifications

Human Tumor Marker CA125 ELISA Test Kit
Tumor Marker Tests:

 

Category No.

Device Name

10101

AFP

10103

CA125

10104

CA153

10105

CA199

10111

NSE

10107

Free β-HCG

10106

CEA

10109

PSA

10108

Free PSA

10110

PSA 45min

 

 

 

AFP ELISA kit

 

 

Name

AFP ELISA Test

Full name

Human AFP (Alpha Fetoprotein) ELISA Test Kit

Category Name

Cancer ELISA kits

Test

96

Method

ELISA method: Enzyme Linked Immunosorbent Assay

Principle

Sandwich Complex

Detection Range

0-300 ng/mL

Sample

20ul serum

Specificity

98.5%

Sensitivity

2.0 ng/mL

Total Time

~80min

Shelf Life

12-14 Months from the manufacturing date

 

 AFP ELISA kit description:


AFP ELISA test kit is an Enzyme Immunoassay test intended for the quantitative determination of AFP concentration in human serum.

Materials Provided with AFP ELISA Kit:
1. Microtiter wells coated with AFP ELISA Antibody
2. Zero buffer 
3. Reference standard set: 0, 5, 20, 50, 150 & 300 ng/ml
4. AFP EIA Kit Enzyme Conjugate Reagent
5. TMB Substrate
6. AFP Elisa Test Stop Solution
7. Wash Buffer Concentrate 50X

Materials Required, not Provided:
1. Precision pipettes
2. Distilled or deionized water
3. EIA kit Microplate Washer
4. EIA kit Microplate Reader with a 450 nm 

AFP ELISA Kit Background Information:
Elevation of serum AFP to abnormally high values, occurs in several malignant diseases, most notably non-seminomatous testicular cancer and primary hepatocellular carcinoma. In the case of non-seminomatous testicular cancer, a direct relationship has been observed between the incidence of elevated AFP levels and the stage of disease. Elevated AFP levels have also been observed in patients diagnosed with seminoma with non-seminomatous elements, but not in patients with pure seminoma. In addition, elevated serum AFP concentrations have been measured in patients with other noncancerous diseases, including ataxia telangiectasia, hereditary tyrosinemia, neonatal hyperbilirubinemia, acute viral hepatitis, chronic active hepatitis, and cirrhosis. Elevated serum AFP concentrations are also observed in pregnant women. Therefore, the AFP ELISA test kit measurements are not recommended for use as a screening procedure to detect the presence of cancer in the general population. 

AFP ELISA Test Principle:
The AFP ELISA kit is based on a solid phase enzyme-linked immunosorbent assay. The AFP ELISA kit utilizes one anti-AFP antibody for microtiter wells immobilization and another with mouse monoclonal anti-AFP antibody in the antibody-enzyme horseradish peroxidase conjugate solution. In the AFP ELISA kit, the serum is added to the AFP antibody coated microtiter wells and incubated with the Zero Buffer. If human AFP is present in the specimen, it will combine with the antibody on the well. For additional details please refer to the instructions for use.

Notable features of Cancer ELISA Kits:
User-friendly directions and explanation of test procedures
Simple and safe reagent preparation
Clear instructions on specimen collection
Comprehensive package of required materials
Explicit quality control and storage guidelines
Reliable and easy-to-read test results