| Payment Terms | TT 100% PAYMENT |
| Supply Ability | 100000 |
| Delivery Time | 7-15 days |
| Packaging Details | CARTON |
| Country of Origin | China |
| Format | Kit |
| Shelf Life | 18 Months |
| Specificity | High |
| Assay Time | 1.5-3 Hours |
| Test Type | AFP Alpha Fetoprotein Elisa Test Kit |
| Kit Size | 96 Tests |
| Sample Type | Serum, Plasma, |
| Brand Name | Biovantion |
| Model Number | TY0027 |
| Certification | ISO13485 |
| Place of Origin | China |
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Product Specification
| Payment Terms | TT 100% PAYMENT | Supply Ability | 100000 |
| Delivery Time | 7-15 days | Packaging Details | CARTON |
| Country of Origin | China | Format | Kit |
| Shelf Life | 18 Months | Specificity | High |
| Assay Time | 1.5-3 Hours | Test Type | AFP Alpha Fetoprotein Elisa Test Kit |
| Kit Size | 96 Tests | Sample Type | Serum, Plasma, |
| Brand Name | Biovantion | Model Number | TY0027 |
| Certification | ISO13485 | Place of Origin | China |
| High Light | Enzyme Linked Elisa Test Kit ,AFP Alpha Fetoprotein Elisa Test Kit ,Short Transport Time Elisa Test Kit | ||
The AFP assay is an enzyme-linked immunosorbent assay (ELISA) for the in vitro quantitative determination of alpha fetoprotein (AFP) in Human serum.
AFP is a glycoprotein with a molecular weight of between 65,000 and 70,000 Daltons including 4% of carbohydrate during fetal development, AFP maintains high levels in the serum and drops to very low levels throughout the remainder of life.AFP is elevated in the malignant diseases of hepatocelluar, testicular nonseminomatous origin, and occasionally of other endodermis origin AFP may be slightly elevated or persisted in the patients with large hepatic metastases or viral hepatitis. AFP measurement is widely accepted as tumor marker and for monitoring .the therapeutic effectiveness of hepatocellular cancer and nonseminomatous testicular cancer. The highest AFP concentration appears in the amniotic fluid in the earliest stages of pregnancy, and diminishes in concentration through the remainder of the pregnancy. Elevated AFP levels in the amniotic fluid were found in fetus with open neural tube defects, e. g. spinal bifida or anencephaly also were found in fetus with severe fetal hemolytic disease, omphalocele, esophageal atresia, congenital nephrosis, intrauterine death, or fetal bleeding into the amniotic fluid. For diagnostic purpose, ultrasonography and acetyicholinesterase measurement should be performed in conjunction with the measurement of AFP. 1,2,3 The AFP assay provides an enzyme immunoassay system with high sensitivity for human AFP measurement in serum.
Sandwich principle.
Total duration of assay: 50 minutes.
The AFP assay is a quantitative solid phase enzyme-linked immunosorbent assay (ELISA).The wells are coated with anti-AFP antibodies. The samples, Standards and Controls are incubated in the wells with enzyme conjugate which is another antibody directed toward a different region of AFP molecules and chemically conjugated with horseradish peroxidase. Unbound enzyme conjugate is washed off and the amount of bound peroxidase is proportional to the concentration of the AFP present in the Samples, Standards and Controls, the intensity of color developed is proportional to the concentration of AFP in the serum, The optical density of the colored samples is read with a microplate reader at 450 nm.
Technical Parameters:
| Product Name: | AFP Alpha Fetoprotein Elisa Test Kit |
| Manufacturer: | Biovantion |
| Format: | Kit |
| Applications: | Diagnosis |
| Assay Time: | 2-3 Hours |
| Sample Type: | Serum, Plasma |
| Specificity: | High |
| Sensitivity: | High |
| Shelf Life: | 18 Months |
| Kit Size: | 96 Tests |
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• Human serum is recommended for this assay.
• Cap and store the samples at 18-25 ℃ for no more than 8 hours. Stable for 7 days at 2-8℃, and 1 month at -20℃. Freeze only once.
• Do not use heat-inactivated samples.
• Sediments and suspended solids in samples may interfere with the test result which should be removed by centrifugation. Ensure that complete clot formation in serum samples has taken place prior to centrifugation.
• Avoid grossly hemolytic, lipemic or turbid samples.
Q: What is the brand name of this test kit?
A: The brand name of this test kit is Biovantion.
Q: Where is this test kit manufactured?
A: This test kit is manufactured in China.
Q: Is this test kit certified?
A: Yes, this test kit is certified with ISO13485.
Q: What is the minimum order quantity for this product?
A: The minimum order quantity for this product is 10.
Q: What is the packaging details for this product?
A: The packaging details for this product is CARTON.
Q: What is the delivery time for this product?
A: The delivery time for this product is 7-15 days.
Q: What are the payment terms for this product?
A: The payment terms for this product is TT 100% PAYMENT.
Q: What is the supply ability for this product?
A: The supply ability for this product is 100000.
Q: Is the price of this product negotiable?
A: Yes, the price of this product is negotiable.
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Biovantion Inc is independent from international department of Bioneovan Co., Ltd., which established in 2 0 0 5, is an in vitro diagnostic reagents manufacturer engaged in the research, development, production, and focus on clinical testing for infectious diseases, such as Hepatitis virus, Noro vir... Biovantion Inc is independent from international department of Bioneovan Co., Ltd., which established in 2 0 0 5, is an in vitro diagnostic reagents manufacturer engaged in the research, development, production, and focus on clinical testing for infectious diseases, such as Hepatitis virus, Noro vir...
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