General Information One-Step Ractopamine Rapid Test does not require any equipment for the detection of pig urine,Tissue and Feed Ractopamine residues. Detection limit: 3ppb Specimen: Urine, Tissue ,Feed Reading Time :3-5 min
1. The One Step RV IgG/IgM Test can be performed used on Whole Blood /Serum / Plasma. 2. To collect whole blood, serum or plasma specimens following regular clinical laboratory procedures. 3. Testing should be performed immediately after specimen collection. Do not leave the specimens at room temperature for prolonged periods. For long term storage, specimens should be kept below -20â??. Whole blood should be stored at 2-8â?? if the test is to be run within 2 days of collection. Do not freeze whole blood specimens. 4. Bring specimens to room temperature prior to testing. Frozen specimens must be completely thawed and mixed well prior to testing. Specimens should not be frozen and thawed repeatedly. Test Procedure Allow the test, specimen, buffer and/or controls to reach room temperature 15-30â?? (59-86â??) prior to testing. 1. Bring the pouch to room temperature before opening it. Remove the test device from the sealed pouch and use it as soon as possible. 2. Place the test device on a clean and level surface. 3. Hold the dropper vertically and transfer 1 drop of specimen (approximately 10μl) to the specimen well(S) of the test device, then add 2 drops of buffer (approximately 80μl) and start the timer. See illustration below. 4. Wait for the colored line(s) to appear. Read results at 15 minutes. Do not interpret the result after 20 minutes. Interpretation of Results Positive: Control line and at least one test line appear on the membrane. The appearance of T2 test line indicates the presence of RV specific IgG antibodies. The appearance of T1 test line indicates the presence of RV specific IgM antibodies. And if both T1 and T2 line appear, it indicates that the presence of both RV specific IgG and IgM antibodies. The lower the antibody concentration is, the weaker the result line is. Negative: One colored line appears in the control region(C). No apparent colored line appear in the test line region. Invalid: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test device. If the problem persists, discontinue using the test kit immediately and contact your local distributor.
General information One-step influenza a/b test is detection influenza type a and type b nucleoprotein antigen extracted from the nasal swab specimen. Sensitivity : 91.3% , specificity : 95.7% Detection limit:5.1x105tcid50/ml Specimen: nasal swab Reading time : 15-20min
Uncut Sheet Toxoplasma Gondii IgG/IgM Tri-Lines Rapid Test Specimen :Whold Blood/Serum/Plasma INTENDED USE The One Step TOXO IgG/IgM Test is a rapid chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to Toxoplasma gondii in Whole Blood /Serum / Plasma to aid in the diagnosis of TOXO infection. Toxoplasma gondii is an obligate intracellular protozoan parasite with a worldwide distribution. Serological data indicates that approximately 30% of the population of most industrialized nations is chronically infected with the organism. A variety of serologic tests for antibodies to Toxoplasma gondii have been used as an aid in diagnosis of acute infection and to assess previous exposure to the organism. These tests are the Sabin-Feldman dye test, direct agglutination, indirect hemagglutination, latex agglutination, indirect immunofluorescence, and ELISA. Recently, lateral flow chromatographic immunoassay, such as The Toxo IgM/IgG Rapid Test (Whole Blood/Serum/Plasma) was introduced into the clinic for the serodiagnosis of Toxoplasma gondii infection. One step TOXO IgG/IgM Test is a simple, visual qualitative test that detects TOXO antibodies in human Whole Blood/serum/plasma. The test is based on immunochromatography and can give a result within 15 minutes. Storage and Stability Store as packaged in the sealed pouch at room temperature or refrigerated (4-30â?? or 40-86â??). The test device is stable through the expiration date printed on the sealed pouch. The test must remain in the sealed pouch until use.
INTENDED USE The HCG s/u Gold Rapid Screen Test(RST)is a chromatographic immunoassay for the early detection of human chronic gonadotropin (HCG) in serum/plasma or urine specimens. INTRODUCTION HCG is a glycoprotein hormone secreted by the developing placenta during pregnancy. The concentration of HCG in serum is approximately equal to the concentration in urine. The concentrations of HCG in urine and serum continue to rise during the first trimester of pregnancy to as high as 100,000 mIU/ml. HCG appears in urine shortly after conception, and continues to increase during the early stages of pregnancy, making it an excellent indicator for the detection of pregnancy. PRINCIPLE The membrane of the test device was coated with anti HCG antibodies on the test region and goat anti mouse IgG antibodies on the control region. During the test, urine specimen is allowed to react with the HCG monoclonal antibody-colloid gold conjugate, which was pre-dried on the test strip. The mixture then moves upward on the membrane chromatographically by capillary action. For a positive specimen, the conjugate binds to the HCG forming an antibody-antigen complex. This complex is captured by anti HCG antibody immobilized on the test region (T) and produces a pink color band when HCG concentration is equal to or greater than 25mIU/ml. Absence of this colored band in the test region suggests a negative result. To serve as a procedural control, a colored band at the control region(C) will always appear regardless the presence or absence of HCG. STORAGE
INTENDED USE Giardia Ag Feces Rapid Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of Giardia antigen in feces. Assay Time: 5-10 min Sample: Feces PRINCIPLE Giardia Ag Feces Rapid Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window. The testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough Giardia 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 Giardia antigen in the sample..
Drug abuse screening tests supply, multiple test items that are available, directly from the factory.
The CorDx HCG PREGNANCY TEST MIDSTREAM KIT FOR SELF TESTING is a rapid test for the qualitative detection of human chorionic gonadotropin (hCG) in urine species to aid in the early detection of pregnancy. It is intended for home users and for prescription use. Featuresï¼? accuracy>99.5% sensitivity: 25miu /ml rapid: result is readable as quick as in 1 minute. specimen: urine, widely used for self-testing. shelf life: 36months or 24months packing:1pc/box, 3pcs/box CE and FDA approved
Product Name : Diagnostic Kit for Antibody IgM/IgG of Novel Coronavirus COVID-19 (Colloidal Gold Immunochromatography Assay) Product Description : COVID-19 Pathogen:SARS-CoV-2 Severe Acute Respiratory Syndrome Coronavirus 2, The strain of coronavirus became officially known as the severe, acute respiratory syndrome coronavirus 2 (SARS-CoV-2), and also, referred to as 2019-nCoV. The infection caused by this virus is, known as coronavirus disease-2019 (COVID-19) . 2019-nCoV is a, beta-coronavirus, as are the viruses that cause severe acute, respiratory syndrome (SARS) and Middle East respiratory syndrome, (MERS) . These viruses are zoonotic (i.e. transmitted between, animals and humans) and have their origins in bats. Most people, become infected with these viruses at some point in their lives, and, usually the duration of illness is short. However, a comprehensive, clinical picture of COVID-19 is still not entirely clear . Price of product ( USD price or FOB price) : FOB price:US$45,134 Product origin : China Key Specifications/Special Features : CE \TUV Minimum Order Size and Packgaing details :
INTENDED USE For qualitative detection of the nucleocapsid protein antigen of SARS-CoV-2 in nasopharyngeal and nasal swab, and saliva specimens from individuals and is aid in rapid diagnosis of patients with suspected SARS-CoV-2 infection. FEATURES Carefully selected special monoclonal antibody to the nucleocapsid protein antigen from SARS-CoV-2. Various applicable specimen: Nasopharyngeal swab, Nasal swab and Saliva. Easy to use, easy results interpretation by naked eyes. Test result available within 15minutes. TEST PROCEDURE: Very simple as per the instructions stated on the manual inserted in the kit. RESULTS INTERPRETATION Positive: A red line appears on the test line (T) and the control line (C). NOTE: A positive result does not rule out co-infections with other pathogens. Negative: Only the control line (C) appears, and no red line appears on the test line (T). NOTE: A negative result does not exclude infection. Invalid: There is no red line at the position of the control line (C). Regardless of whether the TEST line (T) is displayed, it is an invalid result and the sample should be tested again. CLINICAL PERFORMANCE SARS-CoV-2 Antigen Test Kit Comparator Method (NTA) Positive Negative Total Positive 97 0 97 Negative 3 100 103 Total 100 100 200 - Positive Agreement (95% CI): 97/100 97% (83.3% - 99.9%) - Negative Agreement (95% CI): 100/100 100.0% (95.5% - 100%) - LoD: 1.5�??102 TCID50 for virus lysate, 10pg/mL for recombinant Nucleocapsid protein antigen. - Compared with NAT method, the specimens with the Ct range between 30-35 will be detectable. - No cross-reactions with various bacteria, viruses and fungi normally available in respiratory track. - Positive Agreement (95% CI): 97/100, 97% (83.3% - 99.9%) - Negative Agreement (95% CI): 100/100, 100.0% (95.5% - 100%). [Product Name]: SARS-CoV-2 Antigen Test [Product Code]: Cat# FP-318 [Sample Type]: Nasopharyngeal swab / Nasal swab /Saliva [Detection Method]: Colloidal Gold [Reaction Time]: Within 15min [Packing Size]: 1T x 20 cassettes + Sample buffer 20 vials x 0.5mL + 20 samples collection swab x 1. [Storage Conditions]: 2*C ~ 30*C [Shelf Life]: 12 months [CE Mark Registration No.]: RPS/99/2021.
SARS-CoV-2 IgM/IgG Antibody Test (Colloidal Gold) Origin: China Certification/Registration: NMPA, CE Specimens: WholeBlood / Serum / Plasma Relative Sensitivity: 88.89% Relative Specificity: 100.00% Accuracy: 91.07% Results in 15 minutes Simultaneous detection of IgM/IgG antibodies thereby minimizing risk of missed detection. No equipment needed, suitable for on-site screening. Package: 25T/box, 1000T/CTN CTN Size: 60*40*37 cm G.W./N.W.: 13/12 kgs
Our covid-19 antigen saliva test already got Germany BFARM number, hope to cooerate with your esteemed company, and very soon we will be in PEI list, hope to cooperate with your esteemed company, and we got very good feedback from many clients, promise you high quality. Covid Antigen Ag saliva rapid test card, Sensitivity: 97.1% Specificity: 99% Agreement: 99.57%
How to use swab virus preservation solution 1. Before sampling, mark relevant sample information on the label of sampling tube. 2. According to different sampling requirements, use sampling swab to sample in corresponding parts. The specific sampling methods are as follows: a) Nasal swab: gently insert the swab head into the nasopalatine part of the nasal meatus, stay for a while, and then slowly rotate to exit. The other swab swabs the other nostril, immerses the swab head in the sampling solution, and discards the tail. (suitable for sampling with this product) b) Pharyngeal swab: wipe bilateral pharyngeal tonsils and posterior pharyngeal wall with swab. Similarly, immerse the swab head in the sampling solution and discard the tail. (suitable for sampling with this product) 3. Quickly put the swab into the sampling tube (including virus transport fluid). 4. Break the sampling swab at the broken place and tighten the tube cover. 5. Freshly collected clinical specimens should be transported to the laboratory within 96 hours at 4 - normal temperature, and those that cannot be transported to the laboratory within 96 hours should be stored at - 70 â?? or below. The samples should be extracted as soon as possible after being sent to the laboratory. The samples that can be extracted within 24 hours can be stored at 4. If not, they should be stored at - 70 or below
The sampling swab uses advanced jet implanted nylon fuzz technology. Compared with conventional fiber swabs, the sample is easily penetrated, diluted, and trapped in the fiber. The nylon flocking swab has outstanding sample collection and release capability, and the release rate can reach 90%, which is much higher than that of the conventional fiber swab. Light red media formation contains antibiotics that can effectively inhibit the reproduction of bacteria and fungi.
Covid Ab IgG/IgM Ab Whole blood test device Sensitivity: 86.94% Specificity: 99.31% Accuracy: 93.36% � Covid Antigen Ag swab rapid test card Sensitivity: 96.17% Specificity: >99.9% Accuracy: 98.79% � Covid Antigen Ag saliva rapid test card Sensitivity: 97.1% Specificity: >99.9% Accuracy: 99.57%
Covid Antigen Ag swab rapid test card Sensitivity: 96.17% Specificity: >99.9% Accuracy: 98.79% � Covid Antigen Ag saliva rapid test card Sensitivity: 97.1% Specificity: >99.9% Accuracy: 99.57%
Product Name: COVID-19 IgG/IgM TEST KIT(Colloidal Gold Method) HS code: 3002.15 Packing: 40Kits/Box; 36Box/Carton(1440pcs/Carton); Diluents: 2 bottles/Box. Carton size: 56*43*40CM Gross Weight: 15 KG/Carton.
The new crown virus has broken the otherwise peaceful life and messed up people's lives. It is because of the extremely high risk of infection that everyone is afraid and cautious. When difficulties arise, methods to solve them will follow. In order to determine whether they are infected with the new crown virus, nucleic acid testing has made its debut. Nucleic acid testing is an important means to confirm the new coronavirus, and it is also one of the important processes for patients to confirm the diagnosis. To do nucleic acid testing, Nucleic acid detection has the characteristics of early diagnosis, high sensitivity and specificity, and is the "gold standard" for diagnosing new coronary pneumonia. Currently, the most widely used real-time fluorescent quantitative RT-PCR technology. Generally, the two targets located on the ORF1ab and N genes of the virus are detected. The same specimen must meet the double target positive or the repeated test as single target positive, or the two specimens must meet the single target at the same time to confirm the positive of SARS-CoV-2 virus nucleic acid. The virus transport medium developed by Desheng for the new coronavirus is inactivated and non-inactivated. The nucleic acid detection mainly uses an inactivated virus transport medium, which can instantly crack the pathogen and release the nucleic acid, and the protective agent can prevent the nucleic acid from being degraded. . By fully mixing the collected sample with the virus lysis solution and the virus nucleic acid preservation solution, the virus in the sample can be inactivated. Colleagues can effectively ensure the integrity of the virus nucleic acid in the sample. The collected sample can be transported and processed under normal temperature conditions. Long-term preservation. The saved viral RNA samples can be widely used in genetic testing, enzyme-linked immunoassay (ELISA), PCR testing, etc. Although Desheng does not currently have the technology to produce nucleic acid detection kits, it can produce virus preservation solutions, disposable virus sampling tubes and biological buffers required for nucleic acid detection, as well as luminol and acridine as the raw materials for antigen and antibody detection. ester. Desheng is willing to contribute its part in the fight against the epidemic, and is willing to fight for the cause of human health.
Product Name : COVID-19 SARS-CoV-2 IgM Antibody Test Kit Product Description : Material attachment is good. The shell of the detection card should be flat, the upper and lower covers should be closed evenly, and there should be no obviousgap.Thediluentshouldbeclearandfree offoreignmatter. 1.6 Size:thesizeofteststripshouldnotbelessthan2.5mm. 1.7 Liquidmigrationspeedshouldnotbelessthan10mm/min. 2.Minimumdetectionlimit TheminimumtestlimitreferenceproductsS1shouldbenegative,S2andS3shouldbepositive. 3.Negativecompliancerate 5copiesofnegativereferenceproductsof thetestcompanyshallbeallnegative,withanegativecompliancerateof100%. 4.Positivecompliancerate 5copiesofnegativereferenceproductsof thetestcompanyshallbeallpositive,withanegativecompliancerateof 100%. 5.Repeatability Test1copyoftheenterprisepositivereference,test10times,shouldbeconsistentcolor,arepositive. 6.Specificity 6.4 Cross Reaction: This product with vice influenza virus antibodies, influenza a virus, influenza b virus antibodies, pneumonia chlamydia, mycoplasma pneumoniae antibody, adenovirus antibody, respiratory syncytial virus antibody, hepatitisbsurfaceantibody,hepatitis cvirusantibody,treponemapallidumantibody,humanimmunodeficiencyvirus(HIV) antibodies,EBvirusantibody,measlesvirus,CMVantibodies,enterovirustype71,mumpsvirusantibody,varicella - zoster viruspositivesamples nocrossreaction. 6.5 Thereisnocross-reactionbetweenRF,ANAandAMA. 6.6 Interferingsubstance: (3) When bilirubin concentration =250 mol/L, hemoglobin content =9g/L, triglyceride content =15mmol/L,content of rheumatoid factor =80IU/mL, titer ofANA=1:240, anti-mitochondrial antibody (AMA) =80U/mL, content of mouse IgG=1000g/mL,therewillbenointerferencewiththetestresultsof thisproduct. (4) The commonly used antiviral drugs epiztin acid (=4mg/L), ribavirin (=40mg/L), interferon (=200mg/L), oseltamivir (=30mg/L), abidol (=40mg/L), levofloxacin (=200mg/L), azithromycin (=100mg/L), ceftriaxone (=400mg/L), meropenan(=200mg/L) havenointerferenceinthedetectionofthisproduct. 7. Hookeffect No hook effect was found in the test results of this product within the titer range of clinically positive samples of the novel coronavirusantibody. Price of product ( USD price or FOB price) : $4.23 Product origin : China Key Specifications/Special Features : CE FDA Hospital professional testing and use, family and individuals can not use Minimum Order Size and Packgaing details: MOQ:10000pieces 25pieces/box box size:15*14*6.5cm ,150g/box 100boxes /CTN,CTN Size 72*62*36cm 21KG(without lancet and alcohol cotton)
Product Name : COVID-19 SARS-CoV-2 IgG/Ig Manti body Test Kit (Colloidal Gold) with CE and FDA Product Description : shouldbenoobviousgap.The inner teststrip shouldbefirmlyattachedwithoutwaggle.Thediluentshouldbeclearandfreeof foreignmatter. 1.2 Size:thesizeoftheinnerstripshouldnotbelessthan2.5mm. 1.3 Liquidmigrationspeedshouldnotbelessthan10mm/min. 1.4 2. Minimum detection limit The minimum test limit reference products S1 should be negative, S2 and S3 should be positive. 3. Negative compliance rate:5 pieces of negative referenceproducts of the test companyshall be all negative, with a negative compliancerateof100%. 4.Positivecompliancerate:5pieces of positivereferenceproducts,eachreferencetestonetimes andshallbeallpositive,with apositivecompliancerateof 100%. 5.Repeatability:Test1pieceoftheenterprisepositivereference,testit10times,thecolor shouldbeconsistentandallpositive. 6.Specificity 6.1 Cross Reaction: This product do not cross-react with the positive specimens including vice influenza virus antibodies, influenza a virus, influenza b virus antibodies, pneumonia chlamydia, mycoplasma pneumoniae antibody, adenovirus antibody, respiratory syncytial virus antibody, hepatitis b surface antibody, hepatitis c virus antibody, treponema pallidum antibody,human immunodeficiencyvirus (HIV) antibodies, EBvirus antibody,measles virus,CMVantibodies, enterovirus type71,mumpsvirusantibody,varicella- zostervirus. 6.2 Thereisnocross-reactionbetweenRF,ANAandAMA. 6.3 Interferingsubstance: (1) When bilirubin concentration 250 mol/L, hemoglobin content 9g/L, triglyceride content 15mmol/L, content of rheumatoid factor 80IU/mL, titer ofANA1:240, anti-mitochondrial antibody (AMA) 80U/mL, content of mouse IgG1000g/mL,therewillbenointerferencewiththetestresultsofthisproduct. (2) The commonly used antiviral drugs epiztin acid (4mg/L), ribavirin (40mg/L), interferon (200mg/L), oseltamivir (30mg/L), abidol (40mg/L), levofloxacin (200mg/L), azithromycin (100mg/L), ceftriaxone (400mg/L), meropenan(200mg/L) hasnointerferenceinthedetectionofthisproduct. 7. Hook effect: No hook effect was found inthe test results of this product within the titer range of clinically positive samples ofthenovelcoronavirusantibody. 8. The minimum detection limit and reproducibility of 10 samples of clinically positive serum of COVID-19 novel coronavirus werestudied. Product origin : China Key Specifications/Special Features : CE FDA Hospital professional testing and use, family and individuals can not use Minimum Order Size and Packgaing details: MOQ:10000pieces 25pieces/box box size:15*14*6.5cm ,150g/box 100boxes /CTN CTN Size 72*62*36cm 21KG(without lancet and alcohol cotton)
