The C-Reactive Protein Semi-Quantitative Rapid Test Device (Whole Blood/Serum/Plasma)is a rapid chromatographic immunoassay for semi-quantitative detection of C-Reactive Protein in whole blood, serum or plasma specimens to aid in evaluating risk of cardiovascular disease.
The CK-MB Rapid Test Cassette (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of human CK-MB in whole blood, serum or plasma as an aid in the diagnosis of myocardial infarction (MI).
Gut health is very important in order to maintain healthy life. The gut microbiome test which can be taken in the comfort of your home can reveal any imbalance in your gut flora. You can take corrective action to reduce your risk of diseases like Irritable Bowel Syndrome, diabetes, obesity, depression and hypertension caused by an unhealthy gut.
Product Name
Human Chorionic Gonadotropin (HCG) Test Kit (Immunofluorescence Chromatography)
Purpose
To detect the content of HCG in human plasma/serum/whole blood in vitro quantitatively.For Professional Use only.
Principles of Detection
The HCG Test is a fluorescent lateral flow immunoassay. The test consists of: 1) a conjugate pad containing HCG antibody conjugated with fluorescent microspheres and a control antibody (goat anti-chicken IgY antibody) conjugated with fluorescence microspheres, 2) a nitrocellulose membrane strip containing a test line (T line) and a control line (C line). The T line is pre-coated with another HCG antibody, and the C line is pre-coated with a control line antibody (chicken IgY antibody).
HCG concentration in specimen is positively correlated with the fluorescent density of the microspheres, after the measure and calculation of the quantitative fluorescence immunoassay analyzer, then the analyzer would calculate the concentration of HCG according to the preset calibration curve in the machine and display the result, detection unit is mIU/mL. C line should appear in any cases, which indicates the reaction system is effective.
Storage conditions and shelf life
Store in a sealed aluminum foil bag at 2 - 30 C. After unpacking the aluminum foil bag under temperature 20~30 C , humidity 35~65%, please use it immediately.
Shelf life 18 months.
Product Name
Triiodothyronine (T3) Test Kit (Immunofluorescence Chromatography)
Purpose
To detect the content of T3 in human plasma/serum/whole blood in vitro quantitatively.For Professional Use only.
Principles of Detection
The T3 Test is a fluorescent lateral flow immunoassay. The test consists of: 1) a conjugate pad containing T3 antibody conjugated with fluorescent microspheres and a control antibody (goat anti-chicken IgY antibody) conjugated with fluorescence microspheres, 2) a nitrocellulose membrane strip containing a test line (T line) and a control line (C line). The T line is pre-coated with another T3 antigen, and the C line is pre-coated with a control line antibody (chicken IgY antibody).
T3 concentration in specimen is positively correlated with the fluorescent density of the microspheres, after the measure and calculation of the quantitative fluorescence immunoassay analyzer, then the analyzer would calculate the concentration of T3 according to the preset calibration curve in the machine and display the result, detection unit is nmol/mL. C line should appear in any cases, which indicates the reaction system is effective.
Storage conditions and shelf life
Store in a sealed aluminum foil bag at 2~30�°C. After unpacking the aluminum foil bag under temperature 20~30 �ºC , humidity 35~65%, please use it immediately.
Shelf life 18 months.
Reference range
Reference value:The 95% concentrations of T3 in 239 non-stationary subjects without any obvious thyroid dysfunction ranged from 1.34 to 2.73nmol/L, with a median of 1.81nmol/L;The reference value has been verified with reference to similar products already on the market. Each laboratory can build own reference range according to actual situation.
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Product Name
C-reactive Protein(CRP)Test Kit (Immunofluorescence Chromatography)
Purpose
To detect the content of CRP in human plasma/serum/whole blood in vitro quantitatively.For Professional Use only.
Principles of Detection
The CRP Test is a fluorescent lateral flow immunoassay. The test consists of: 1) a conjugate pad containing CRP antibody conjugated with fluorescent microspheres and a control antibody (goat anti-rabbit IgG antibody) conjugated with fluorescence microspheres, 2) a nitrocellulose membrane strip containing a test line (T line) and a control line (C line). The T line is pre-coated with another CRP antibody, and the C line is pre-coated with a control line antibody (rabbit IgG antibody).
CRP concentration in specimen is positively correlated with the fluorescent density of the microspheres, after the measure and calculation of the quantitative fluorescence immunoassay analyzer, then the analyzer would calculate the concentration of CRP according to the preset calibration curve in the machine and display the result, detection unit is mg/L. C line should appear in any cases, which indicates the reaction system is effective.
Product Name
Fecal Occult Blood(FOB)Test Kit (Colloidal Gold Method)
Purpose
To detect the content of FOB in human fecal in vitro qualitatively.For Professional Use only.
Principles of Detection
The FOB Rapid Test is a one-step chromatographic sandwich immunoassay. The test consists of: 1) a conjugate pad containing HB monoclonal antibody conjugated with colloidal gold. 2) a nitrocellulose membrane strip containing a test line (T line) and a control line (C line). The T line is pre-coated with another HB antibody, and the C line is pre-coated with a control line antibody (goat-anti-mouse IgG antibody).
After addition of the sample, FOB will bind with a colloidal gold-labeled antibody on the conjugate release pad. The resulting complex flows over the nitrocellulose membrane where a specific capture reagent is pre-coated and a red line can be seen at the test zone (T). Unreacted colloidal gold-labeled antibodies in the sample are captured at the control zone (C). The intensity and speed at which the color develops depend on the FOB concentration in the sample.
Reference range
This kit can detect FOB at a minimum of 50ng/ml.
Performance Characteristics
1. Critical value and repeatability:
1) The quality control substance of FOB with a concentration of 50ug/mL was detected for 20 times, and the positive coincidence rate was â?¥95%, and the color uniformity, and the reaction results were consistent.
2) The quality control substance of FOB with a concentration of 10ng/mL was detected for 20 times, and the negative coincidence rate was â?¥95%, and the color uniformity, and the reaction results were consistent.
2. Analysis specificity: 500ug/mL bovine HB,500ug/mL pork HB,500ug/ mL chicken HB,500ug/mL goat HB,2000ug/mL Horseradish Peroxidase specific quality control substance were all negative.
3.HOOK effect: human FOB positive quality control substance of 2000ug/mL was detected and the result was positive.
Product Name
Glycosylated Hemoglobin(HbA1c)Test Kit (Immunofluorescence Chromatography)
Purpose
To detect the content of HbA1c in human whole blood in vitro quantitatively.For Professional Use only.
Principles of Detection
The HbA1c Test is a fluorescent lateral flow immunoassay. The test consists of: 1) a conjugate pad containing HbA1c antibody conjugated with fluorescent microspheres and a control antibody (goat anti-chicken IgY antibody) conjugated with fluorescence microspheres, 2) a nitrocellulose membrane strip containing a test line (T line) and a control line (C line). The T line is pre-coated with another HbA1c antibody, and the C line is pre-coated with a control line antibody (chicken IgY antibody).
HbA1c concentration in specimen is positively correlated with the fluorescent density of the microspheres, after the measure and calculation of the quantitative fluorescence immunoassay analyzer, then the analyzer would calculate the concentration of HbA1c according to the preset calibration curve in the machine and display the result, detection unit is %units. C line should appear in any cases, which indicates the reaction system is effective.
Storage conditions and shelf life
Store in a sealed aluminum foil bag at 2~30�°C. After unpacking the aluminum foil bag under temperature 20~30 �ºC , humidity 35~65%, please use it immediately.
Shelf life 18 months.
Specimen collection and preparation
1. Human whole blood samples can be used for this test.
2. Specimen collection:Collect blood specimen into a collection tube containing EDTA , evenly mixed before use. Do not use hemolyzed blood for testing.
Whole blood specimens should be stored at 2-8�°C for no more than 4 hours if not test immediately.
3. Do not test patients' samples with severe hemolysis, lipemia and jaundice, all specimens should be treated as infectant.
4. Restore the specimen to 20-30�°C before the detection, cryopreserved specimen should be completely thawed, rewarmed and evenly mixed before use.
Reference range
Positive: reading value â?¥6%, a positive result.
Negative: reading value 8%, poorly controlled blood glucose.
The reference value is verified with reference to similar products that have been marketed. Due to ethnic and geographical differences, each laboratory can establish its own reference interval according to the actual situation.
Newcastle Ag Rapid test Kit
Features
For rapid detection of Newcastle disease virus antigens
Effective tool for disease detection and diagnosis
The easiest operation and detection tools
Quickly present the result
Economic testing costs
New castle Ab rapid test kit/Avian Influenza Ab rapid test kit
Features
Blocking method unlike other methods of rapid test kit, have a high coincidence rate with hemagglutination inhibition
Convenient and fast detection tools: extremely simple operation, quick present results
Economic testing costs: excellent testing tools, low prices.
Parameters for Newcastle disease Ab rapid test kit
T7 High Yield RNA Synthesis Kit optimizes the transcription reaction system. The kit can synthesize the single-stranded RNA efficiently by uses T7 RNA polymerase, the linear double-stranded DNA with the T7 promoter sequence as the template, NTPs as the substrate to control the DNA sequence downstream of the promoter. During transcription, modified nucleotides can be added to the substrate to prepare biotin or dye-labeled RNA.
This kit can synthesize long transcripts and short transcripts., RNA can be produced 100-200 g with 1 g of template input. The RNA synthesized by transcription can be used for such as RNA structure and function research, RNase protection, probe hybridization, Various downstream applications such as RNA, microinjection and in vitro translation.
CE,ISO 13485
Novel Coronavirus (COVID-19) Nucleic Acid Detection Kit (RT-PCR) is used for nucleic acid detection of the ORF1ab sequence and N gene of the Novel Coronavirus (SARS-CoV-2) in nasopharyngeal swab, oropharyngeal swab, sputum and other specimens.
The primer and probe sets in this kit are designed for the detection of the conserved sequences of SARS-CoV-2 (ORF1ab and N gene). The kit also contains an Internal Control (human RNase P gene) that is used to assess specimen quality and avoid a false negative result. Real-Time PCR technology utilizes polymerase chain reaction (PCR) for the amplification of specific target sequences and target specific probes for the detection of the amplified RNA. The probes are labelled with fluorescent reporter and quencher dyes.
The One Step hCG test is a rapid test to detect the presence of HCG in urine or serum specimens in a qualitative format sensitive to 15mIU HCG/ml. The test utilizes a combination of monoclonal and polyclonal antibody reagents to selectively detect elevated level of HCG in urine or serum. The immunological specificity of the test virtually eliminates cross reactivity interferences from the structurally related glycoprotein hormones hFSH, hLh, hTSH at physiological levels.
SARS-CoV-2 IgG/IgM Cartridge
Kit include : 1 Test Box + 1 Cartridge + 1 UV Touch
SARS-CoV-2 IgG/IgM Kit is used for rapid and accurate screening of the COVID-19, which helps identify suspected patients and
reduce false negative rate. Rapid detection of recent SARS-CoV-2 infection
In ONLY 12 minutes
ONE-STEP operation
Single cartridge, NO additional buffers
TRFIA Europium particles displays Clear and Bright results
Dual capturing antigens (S and N) enhanced sensitivity
Important complement to PCR detection in COVID-19 diagnosis
PCR based test is the gold standard for detection of SARS-CoV-2 infection. The kit is based on the reverse transcription-polymerase chain reaction (RT-PCR), amplifying two target sequences on the viral ORF1ab and N genes, as recommended by both China and U.S. CDC. By monitoring the reaction signal in real-time and comparing with a cut-off Ct value, the virus can be detected qualitatively. The kit contains all necessary components for the RT-PCR assay as well as a positive and a negative template control for quality control.
Two target sequences detected in one tube: Open Reading Frame 1ab (ORF1ab) & SARS-CoV-2 N gene
Stable amplification with good repeatability
Positive and Negative template control for quality assurance
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