Ferritin Quantitative Test

Detection Kit for Monkeypox Virus ( Real-time PCR )


Detection Kit for Monkeypox Virus ( Real-time PCR ) is designed for the qualitative detection of Monkeypox Virus (MPV) DNA extracted from skin, fluid, or crusts collected directly from skin lesions. It's based on real-time PCR technology, the primers and probes target specific sequences of MPV, and do not react with nucleic acids of other pathogens.


Product Detail

Principle

The assay is based on Real-time PCR for qualitative detection of MPV. Fluorogenic probe hydrolysis chemistry is used to generate fluorescent signal when a specifific DNA sequence of MPV is amplified.


Product Specification

Product Name

Detection Kit for Monkeypox Virus ( Real-time PCR )

Specimen Types

Skin/Fluid/Crusts

Storage Condition

2-30°C

Shelf Life

12 Months

Package

48T


Product Features

✔Easy and simple

✔Accurate & high specificity

✔Sensitivity: 250 copies/mL

✔Available for multiple PCR analyzers


Performance

Accuracy: The positive coincidence rate is 100.0%; the negative coincidence rate is 100.0%.

Limit of detection: The tentative LOD was estimated as 20 copies/rxn.

Precision: The CV value of 10 replicates at all positive control was no higher than 5%.


Leave A Message

Please provide us with the information below, and we'll contact you as soon as possible.

Related Products
hs cTnI Rapid Quantitative Test
hs cTnI Rapid Quantitative Test
cTnI, a crucial cardiac biomarker, assists in detecting and managing acute myocardial infarction and assessing patient risk in cardiovascular events. Biotime's hs-cTnI offers high sensitivity, compatibility with versatile samples, and stable performance. Trust our ideal biomarker for comprehensive acute coronary syndrome evaluation.
Biotime LH Rapid Quantitative Test
LH Rapid Quantitative Test
Luteinizing hormone is a hormone produced by gonadotropic cells in the anterior pituitary gland. In females, an acute rise of LH ("LH surge") triggers ovulation and development of the corpus luteum. In males, where LH had also been called interstitial cell‒stimulating hormone (ICSH), it stimulates Leydig cell production of testosterone. It acts synergistically with follicle-stimulating hormone (FSH).
Biotime 3 in 1 (cTnI/CK-MB/Myo) rapid fluorescence immunoassay test
3 in 1 (cTnI/CK-MB/Myo) Rapid Quantitative Test
3 in 1 test kit has a very high specificity and sensitivity for the detection of AMI, making a correct and timely diagnosis for patients with chest pain or clinically suspected AMI, and thus providing validly basis for clinicians with prompt rescue and treatment.
Chemiluminescence Immunoassay
CLi-1600
CLi-1600 semi-automated device which quantifies biomarkers for thyroid disease, inflammation, cardiac diseases, fertility, diabetes, bone metabolism, anemia, and health check by analyzing human serum, plasma and whole blood.
HbA1c Analyzer
HLC-100 Fully Automated HbA1c Analyzer
Biotime’s HLC-100 Fully Automated HbA1c Analyzer provides a prompt, reliable solution for diabetes diagnosis. It utilizes the high performance liquid chromatography (HPLC) analytical technique, a gold standard that helps detect glycosylated hemoglobin (HbA1c) with superior precision. Its capability to measure HbA1c, HbF, and other hemoglobin fragments enables clinicians to make quick, accurate diagnoses, thus facilitating timely treatment for the patient.
Malaria P.f/Pan Antigen Rapid Qualitative Test
Malaria P.f/Pan Antigen Rapid Test
The Malaria P.f/Pan Antigen Rapid Test is a rapid lateral flow immunoassay for the qualitative detection of Histidine-Rich Protein II (HRP-II) specific to Plasmodium falciparum (P.f) and Plasmodium lactate dehydrogenase (pLDH) specific to Plasmodium species (Pan) in human whole blood specimen. It is intended to be used by professionals as a screening test and provides a preliminary test result to aid in the diagnosis of infection with Malaria. For professional in vitro diagnostic use only.
The Dengue NS1 Antigen Qualitative Rapid Test
The Dengue NS1 Antigen Rapid Test
The Dengue NS1 Antigen Rapid Test is a lateral flow immunoassay for the qualitative detection of Dengue virus NS1 antigen in human serum, plasma or whole blood. It is intended to be used by professionals as a screening test and provides a preliminary test result to aid in the diagnosis of infection with the dengue virus. For professional in vitro diagnostic use only.
Incubation Chamber
ICE-100E Incubation Chamber
The incubation chamber is an auxiliary device for Biotime’s fluorescence immunoassay analyzer. The reaction temperature and time is critical for test results. The incubation chamber provides an optimized environment as well as automatic timers for test reactions to improve the reliability of test results.
Leave A Message

Leave A Message

    Please provide us with the information below, and we'll contact you as soon as possible.

Home

products

about

contact