Range of high quality urine pregnancy test kits Each test is over 99% accurate and can detect HcG in urine up to three days prior period due date Choose from a simple dip test, cassette where you drop urine on to the test using the enclosed pipette or a mid stream "home test"
Price depends on the qty.
Export from the UK.
Urine Glucose Test Strips, Insight US001 (50's/pack)
High quality urine test strips for quick analysis of urine specimen. Extremely easy to use and even suitable for self-testing. High resistance to Ascorbic Acid/Vitamin C preventing false negatives. Tests for 2 Parameters - Glucose - Protein.
Price depends on the ordered qty. Made in the UK. Export from the UK.
Insight Urinalysis Test Strips, 8 Parameters (x100). High quality urine test strips for quick analysis of urine specimen. Extremely easy to use and even suitable for self-testing. Simply dip the strip in a urine sample, wait for 30 seconds to 2 minutes and compare the colour change in the strip against the colour chart on the bottle.
Tests for 8 Parameters - Leukocytes - Nitrite - Protein - pH - Blood - Specific Gravity - Ketones - Glucose. Made in the UK. Export from the UK.
Insight Urine Test Strips, 5 Parameters - 50's/pack. Tests for 5 Parameters - Blood - pH - Protein - Ketones - Glucose.
Made in the UK.Export from the UK.
Non-inactivated type: it does not contain lysate, which can maintain the activity and integrity of pathogen, and can be used for virus culture and isolation.
Inactivated type: it can split pathogen instantly and release nucleic acid, and the protective agent can prevent nucleic acid from degradation.
Scope of use
The virus preservation solution can be used for the collection, preservation and transportation of nasopharyngeal pathogen specimens such as new coronavirus, influenza, bird flu, hand-foot-mouth disease, measles and so on.
Non-inactivated type: On the basis of Hank's, BSA (bovine serum albumin) amino acids, vitamins and other nutrients are added to maintain the virus' activity over a wide temperature range and maintain the originality of the sample to the greatest extent and can be used for virus nucleic acid extraction and detection, virus culture and isolation.
Inactivated type: By fully mixing the collected samples with virus lysate and virus nucleic acid preservation solution, the virus in the samples can be inactivated, and the integrity of virus nucleic acid in the samples can be effectively guaranteed. The collected samples can be transported and preserved for a long time under normal temperature. The preserved viral RNA samples can be widely used for genetic testing, enzyme-linked immunoassay (ELISA), PCR testing, ect.
Storage conditions and time
Non-inactivated type: Store at 4-25 It shall be transported to the laboratory within 48 hours under 2-8 after sampling, or stored under - 70
(1) The Q-Sens Covid-19 Detection kit V2 (RT-PCR test kit)
- FOB Korea: 400$ US per kit (100 test/kit)
- Certification: CE-IVD, KFDA
- Using real time reverse transcription polymerase chain reaction (RT-PCR) technology. This product contains enzymes and reaction components required for cDNA synthesis and PCR amplification, so a RT-PCR reaction can be easily performed by one step of adding of RNA template to primer/probe mixture.
- Targets: RdRp gene & E gene
- Specimens: Nasopharyngeal swab, oropharyngeal swab and sputum from patients
- Results within 2 hours
- Packing: 100 tests / kit
- Store at below -20C
(2) The Q-Sens Covid 19 lgG/lgM rapid kit
- FOB Korea: 390$ US per kit (100 test/kit)
- Certification: CE-IVD, KFDA
- Results within 10 min
- Store at 2~30 C
We do have SARS-COV-2 ANTIGEN TEST KIT located in Europe in stock ready to ship. Certificates: CE and ISO
We give facilities in terms of payment; 15-25% with the agreement and the rest after the product arrives to the required country.
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.
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.
HPV NGS Kit is an in vitro diagnostic test that simultaneously detects the genotype of human papillomavirus (HPV) using Next-Generation Sequencing technology (NGS). Automated workflows allow for fewer human errors and less hands-on time from library construction to analysis of results. HPV types are quickly identified by simultaneously analyzing up to 480 samples. NGS time is reduced to approximately 24 hours.
Ezplex HLA-B NGS typing Kit is an in vitro diagnostic test that detects and distinguishes allelic genes of HLA-B in human leukocyte antigens at high resolution using next-generation sequencing. Ezplex's unique amplicon approach simplifies the traditional complex NGS Library construction process and provides dedicated software optimized for HLA typing for easy analysis. The Ezplex HLA-B NGS typing Kit accurately reads the HLA-type Acuracy (95 percent Confidence Interval) in DRB1 Locus within a total of 35 hours from DNA extraction to NGS results analysis to help with pre-transplant testing.
Unique sealing tube test strip series is the main breaking through the invention of amazing biotech, Which can diagnose all the three stages of the covid19 including Virus, antigen, and antibodies.
Here we compare the screening method of different types of testing carried out for Covid-19 including nucleic acid, antigen-based, and antibody-based testing. The comparison is done on the basis of sampling specimen, earliest stage detection, time taken by each, Clinical significance of positive results, Specificity, Sensitivity, and technical difficulty. For nucleic acid testing, the specimen used must be nasopharyngeal swabs, sputum, buffer. For antigen specimen, the specimen must be nasopharyngeal swabs, sputum, buffer, urine. And for antibody-based testing, the specimen used must be plasma and serum. Similarly, the earliest stage detection for nucleic acid testing is after infection, and before symptoms arise. Antigen-based testing is also after infection before symptoms arise and antibody-based testing is One week after symptoms arise. The time taken to carry out the nucleic acid test is 60-180 mins, for antigen test is 10 to 15 minutes and for antibody test is 15 to 180 minutes.
Product Detail
PRINCIPLE
Amazing COVID-19 Antigen Lockseal Tube Test Strip is based on sandwich lateral flow immunochromatographic assay highly sensitively detecting COVID-19 nucleocapsid protein in human nasopharyngeal, nasal secretion, saliva or/and serum specimens, having an invisible T (test) zone and C (control) zone. When the sample is applied into the test tube, the liquid will laterally flow on the surface of the test strip. If there is enough COVID-19 antigen in the sample, a visible T band will appear. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of COVID-19 antigen in the sample.
Specification
V.A: 20/24 kits X 1 pouch/box, 20/24 kits X 5/4 pouches/box
V.B: 20/24 kits X 1 pouch/box, 20/24 kits X 5/4 pouches/box
V.C: Duplex kits X 10/12 pouches/box, Duplex kits X 48/50 pouches/box
V.D: Duplex kits/pouch/box
COVID-19 Ag/Ab Sealing Tube Twin Test Strip (Colloidal Gold)
INTENDED USE:
Amazing COVID-19 Ag/Ab Sealing Tube Twin Test Strip is a lateral flow immuno- chromatographic assay for the simultaneous rapid in vitro differential detection of COVID-19 nucleocapsid protein antigen and COVID-19 antibody (IgG/IgM). The kit has two strips. One strip is for the qualitative detection of COVID-19 nucleocapsid protein antigen in human nasopharyngeal, nasal secretion, saliva or/and serum specimens directly collected from individuals suspected of COVID-19 by their healthcare provider within the first seven days of symptom onset. Another strip is for the qualitative detection of COVID-19 antibody(IgG/IgM) in human serum, plasma (sodium citrate, sodium heparin, dipotassium EDTA), and whole blood (sodium citrate, sodium heparin, dipotassium EDTA or fingerstick whole blood) to aid identifying individuals with an adaptive immune response to COVID-19, indicating recent or prior infection and patients with suspected COVID-19 infection in conjunction with clinical presentation and the results of other laboratory tests. Results from the Amazing COVID-19 Ag/Ab(IgG/IgM) Sealing Tube Twin Test Strip should not be used as the sole basis for diagnosis. The kit is assistance for diagnostic and epidemiological investigation. These two strips are in the sealing tube to avoid potential biosecurity substances such as coronavirus from clinical samples, which will much help to avoid pathogen contamination and spreading to the operator and its environment. The kit is intended for use by medical professionals or trained operators who are proficient in performing tests and trained clinical laboratory personnel or individuals trained in point of care settings.
COVID-19 Ag/Ab(IgG/IgM) Sealing Tube Test Strip (Colloidal Gold):-
INTENDED USE:
Amazing COVID-19 Ag/Ab(IgG/IgM) and Influenza Ag(A/B) Sealing Tube Twin Test Strip is a lateral flow immunochromatographic assay for the simultaneous rapid in vitro differential detection of COVID-19 and Influenza virus.
The kit has two strips. One is for the qualitative detection of COVID-19 nucleocapsid protein antigen and Influenza virus type A in human nasopharyngeal, nasal secretion, saliva or/and serum directly collected from individuals suspected of COVID-19 by their healthcare provider within the first seven days of symptom onset.
Another is for the qualitative detection of COVID-19 antibody(IgG/IgM) in human serum, plasma (sodium citrate, sodium heparin, dipotassium EDTA) and whole blood (sodium citrate, sodium heparin, dipotassium EDTA or fingerstick whole blood) and Influenza virus type B in human nasopharyngeal, nasal secretion, saliva or/and serum specimens to aid identifying individuals with an adaptive immune response to COVID-19, indicating recent or prior infection and patients with suspected COVID-19 infection in conjunction with clinical presentation and the results of other laboratory tests.
Results from the Amazing COVID-19 Ag/Ab(IgG/IgM) and Influenza Ag(A/B) Sealing Tube Twin Test Strip should not be used as the sole basis for diagnosis. The kit is assistance for diagnostic and epidemiological investigation. These two strips are in the sealing tube to avoid potential biosecurity substances such as coronavirus from clinical samples, which will much help to avoid pathogen contamination and spreading to the operator and its environment. The kit is intended for use by medical professionals or trained operators who are proficient in performing tests and trained clinical laboratory personnel or individuals trained in point of care settings.
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On March 23, Lepu SARS-CoV-2 Antigen Test Kit was granted special approval by the German Federal Institute for Drugs and Medical Devices (BfArM) for self-testing in Germany. This allows the users to apply tests at home with the aid of sample nasal swabs.
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