fluorescent AFP ® is suitable for the quantitative detection of AFP concentrations in human serum or plasma. This test cannot be used to guide the diagnosis of paired trisomy 21 for the detection of alpha-fetoprotein (AFP) in human samples. Clinically, it is used for auxiliary diagnosis and treatment monitoring of primary liver cancer. For professional use only.

Certificate: CE Certification

POCT :Point of care test ,result in 15 mins

Automatic:Internal calibration, no manual input

Cost-efficient:One cassette per test, no extra cost

Room Temperature:Store & operate at room temperature

Accurate:High consistency with well-known enterprise


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REF

MF-03

Product Name

 α-Fetoprotein ( AFP ) Diagnostic Kit

Method

Immunochromatographic assay

Qualification

CE

Testing content

α-Fetoprotein ( AFP )

Sample Type

Serum、plasma

Sample

Volume(uL)

70 μL

Working Range

2-300 ng/mL

Reaction Time

min)

15

Storage Temperature

2-30℃

Shelf Life

24 months

Applied Instrument

fluorecare® MF-T1000 Dry-type Immunofluorescence Quantitative Analyzer

Specification

20 tests/kit

25 tests/kit

Size(L*W*H)mm/Kit

145*115*75

205*138*83

Weight(kg)/Kit

0.280

0.337

Kit components

Test Card:20 Cassettes

Diluent:20 tubes

ID Chip:1 Piece

Instruction:1 Copy

Test Card:25 Cassettes

Diluent:25 tubes

ID Chip:1 Piece

Instruction:1 Copy

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