Product Details:
Brand : Thermo Fisher
Model Name/Number : 7500 Fast
Usage/Application : Virus Test Especially Covid-19
Type : Real-Time PCR System
Feature : Simple Intuitive Software
Format : Convenient 96-Eell Format
Peak Block Ramp : 5.5 C/s
Run Time : 36 min
Dynamic Range : 9 Logs Of Linear Dynamic Range
Brand : CTK BIOTECH
Size : 96 Well
Specimen : Serum & Plasma
stored at 2 - 8 C
Cat No : E0100
The RecombiLISA HAV IgM ELISA is a solid-phase enzyme-linked immunosorbent assay for the qualitative detection of IgM anti-hepatitis A virus in human serum or plasma.
Product Features:
Utilizes IgM capture technique
Detects IgM anti-HAV in serum or plasma
Evaluated with BBI HAV serum conversion and HAV mixed titer performance panels
Useful for identifying acute HAV infections
Product Specification:
Microwells coated with anti-human IgM antibody
HAV IgM negative control
HAV IgM positive control
HRP-HAV conjugates
Wash buffer (30 x concentrate)
TMB substrate A
TMB substrate B
Stop solution
ELISA Working Sheet
Product insert
Product Details:
Number of Reactions(Preps)/Kit : 96 Wells
Brand : Abbott
Product Type : Microplate
Sample : Serum
CAT. NO : 11EK50
The presence of circulating non-structural glycoprotein (NS1) indicates Viremia. If sufficient virus is present, NS1 can be detectable in a patientâ??s blood from day 0 to day 5 following disease onset. The detection of NS1 antigen is therefore useful as a test of early acute infection. â?¢ Early diagnosis of dengue infection High accuracy with all dengue serotypes (DEN1,2,3, and 4) Simple and easy to use: All necessary reagents included in the kit â?¢ Shelf life and storage temperature: 18 months from the date of manufacturing at 2-8 'C Performance: Sensitivity 93.3 % (87.4 - 96.6 %), Specificity 98.9 % (96.0 - 99.7 %)
Product Details:
Number of Reactions(Preps)/Kit ; 96 Wells
Brand : InBios
Format : Immunocapture
Specimen : Serum
Cat No : ZKM2-1
The ZIKV Detect 2.0 IgM Capture ELISA is intended for the qualitative detection of Zika virus IgM antibodies in human sera for the presumptive clinical laboratory diagnosis of Zika virus infection. The assay is intended for use only in patients with clinical signs and symptoms consistent with Zika virus infection, and/or CDC Zika virus epidemiological criteria (e.g., history of residence in or travel to a geographic region with active Zika transmission at the time of travel, or other epidemiological criteria for which Zika virus testing may be indicated). Assay results are for the presumptive detection of IgM antibodies to Zika virus (ZIKV). Positive results must be confirmed by following the latest CDC guidelines for the diagnosis of Zika virus infection.
Results of this test are intended to be used in conjunction with clinical observations, patient history, epidemiological information, and other laboratory evidence to make patient management decisions. Zika IgM levels are variable over the course of the infection and may be detectable near day four post onset of symptoms and persist up to approximately 12 weeks following initial infection.
Negative results may be seen in specimens collected before day four post onset of symptoms or after the window of detectable IgM closes, and therefore do not preclude the possibility of Zika virus infection, past or present.
1st Commercial serology kit to receive FDA Marketing Authorization
CE Marked
Differentiates Zika IgM positive patients from those infected with other flaviviruses such as West Nile or Dengue
Sensitivity: >90%
Specificity: >96%
Results in 4 hours
Tests up to 28 unknown specimens.
Size 96 wells/Plate
Format Indirect
Incubation Time 30 + 30 + 5 + 10 + 1
Sample Type Serum
Storage 2-8 C
Cat No STGS-R
The Scrub Typhus Detectâ?¢ IgG ELISA test for exposure to Orientia tsutsugamushi (OT; formerly Rickettsia) is an ELISA assay system for the detection of IgG antibodies in human serum to OT-derived recombinant antigen. For research use only. Not for use in diagnostic procedures.
The complete kit includes one 96 well strippable plate with all necessary reagents and controls.
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Number of Reactions(Preps)/Kit : 96 Wells
Brand : InBios
Sample Material : Serum
Format : ELISA
Incubation Time : 30 + 30 + 5 + 10 + 1
Cat No : STMS-R
The Scrub Typhus Detect IgM ELISA for exposure to Orientia tsutsugamushi (OT; formerly Rickettsia) is an ELISA system for the detection of IgM antibodies in human serum to OT-derived recombinant antigen. This test is for research use only. Not for use in diagnostic procedures.
The complete kit includes one 96 well strippable plate with all necessary reagents and controls.
Product Details:
Quantity/Kit : 96 wells/Plate
Format :Indirect
Brand : InBios
Incubation Time : 30 + 30 +10 + 1
Sample Type : Serum or dried blood spots
Cat No : FILA-1
he Filaria DetectTM IgG4 ELISA is for qualitative detection of specific IgG4 antibodies in specimens to highlyspecific antigen IWb123 target antigen expressed primarily in infective stage larvae (L3) of the lymphatic-dwelling parasite Wuchereria bancrofti (Wb). This product is for research use only. Not for use in diagnostic procedures.
The complete kit includes one 96 well strippable plate with all necessary reagents and controls.
Number of Reactions(Preps)/Kit : 96 Wells
Brand : InBios
Sample Material : Serum
Format : Antigen Detection
Incubation Time : 60+30+20+1
Cat No : DNS1-1
The DENV DetectTM NS1 ELISA is for the early detection of Dengue virus (DENV) NS1 antigen in human serum. This test is for the presumptive clinical laboratory diagnosis of Dengue virus infection. This assay is intended for use in patients with clinical symptoms consistent with either dengue fever or dengue hemorrhagic fever. Samples collected from patients within seven (7) days after the onset of clinical symptoms should be evaluated with this assay (day 0 â?? day 7). Negative results obtained with this test do not preclude the diagnosis of dengue and should not be used as the sole basis for treatment or other patient management decision. This assay is not FDA cleared or approved for testing blood or plasma donors.
The complete kit includes one 96 well strippable plate with all necessary reagents and controls.
FDA Cleared & CE Marked
Early NS1 antigen detection (within first 7 days onset of symptoms)
Helps differentiate dengue from other flaviviruses that may cross react with dengue antibodies but not with the antigen
High Sensitivity & Specificity: 86.6% PPA & 97.8% NPA with prospectively collected positive and negative confirmed clinical specimens
Kit can be performed in parallel with InBiosâ?? FDA Cleared dengue IgM ELISA for presumptive diagnosis of acute or convalescent stage dengue virus.
Number of Reactions(Preps)/Kit : 96 Wells
Brand : InBios
Sample Material : Serum
Format : Immunocapture
Incubation Time : 30+30+30+10
Cat No : CHKM-R
The CHIKjj Detect IgM ELISA is designed for the qualitative detection of IgM antibodies present in human serum targeting Chikungunya virus E2/E1 proteins. This test is not intended to screen blood or blood components. This test is for research use only. Not for use in diagnostic procedures.
The complete kit includes one 96 well strippable plate with all necessary reagents and controls.
Key Features :
InBios chikungunya kits have been developed using a novel technology1 that outperforms traditional antigen preparations, resulting in highly sensitive detection of recent and past CHIKV infection.
Excellent results in CDC evaluation of commercially available chikungunya IgM assays.
Ordering:
Cat No CHKM-R
Formet Immunocapture
Quantity 96 wells/Plate
Incubation Time 30 + 30 + 5 + 10
Sample Type Serum
Storage 2-8
Shelf Life 12 months
Product Details:
Number of Reactions(Preps)/Kit :96 Wells
Brand : InBios
Sample Material : Serum
Formet : Immunocapture
Incubation Time : 30+30+30+10
Cat. No : CHKG-C
CHIKjj Detect : IgG ELISA Kit
The CHIKjj DetectTM IgG ELISA is designed for the qualitative detection of IgG antibodies present in human serum targeting chikungunya virus E2/E1 proteins. This test is for the presumptive clinical laboratory diagnosis of chikungunya virus infection. This assay is intended for use only in patients with clinical symptoms consistent with chikungunya infection.
The complete kit includes one 96 well strippable plate with all necessary reagents and controls.
Key Features :
Developed using a novel technology1 that outperforms traditional antigen preparations, resulting in highly sensitive detection of recent and past CHIKV infection.
>90% Sensitivity and Specificity
DENV Detect and CHIKjj Detect can be run in parallel for differential diagnosis.
CE Marked
Ordering :
Cat No : CHKG-C
Formet : Immunocapture
Quantity : 96 wells/Plate
Incubation Time : 30 + 30 + 5 + 10 + 1
Sample Type : Serum
Storage : 2-8
Shelf Life : 12 months
Number of Reactions(Preps)/Kit : 50
Brand : SD
ICMR Approved : Yes
Result Time (Rapid Kits) : 15 min
Sample Type : Oral & Nasal Swab
STANDARD E Dengue IgM ELISA analyzes IgM antibodies specific to Dengue virus in serum and plasma using enzyme linked immunosorbent assay.
Number of Reactions(Preps)/Kit : 96 Wells
Brand : CTK BioTech
Sample : serum or plasma
Storage : 2-8 c
Cat No : AE0311
INTENDED USE :
The Dengue IgG ELISA is a solid-phase enzyme-linked immunosorbent assay for the qualitative detection of elevated anti-dengue viruses (DEN1, 2, 3, 4) IgG in human serum or plasma. It is intended for professional use only as an aid in the diagnosis of active infection with dengue viruses, including secondary infection.
TEST PRINCIPLE:
The Dengue IgG ELISA Kit is a solid-phase enzyme-linked immunosorbent assay based on the principle of the capture immunoassay methodology for the detection of IgG anti-dengue virus in human serum or plasma. The Dengue IgG ELISA Kit is composed of two key components: 1) Solid microwells pre-coated with mouse monoclonal anti-human IgG antibody. 2) Conjugate composed of biotinylated dengue antigens and avidin HRP-conjugates. During the assay, the test specimen is first incubated in the coated microwell. IgG antidengue, if present in the specimen, binds to the anti-human IgG antibodies coated on the microwell surface, and any unbound specimen is then removed by a wash step. During a second incubation with Biotinylated dengue antigens, the IgG anti-dengue absorbed on the surface of microwell binds with dengue antigen, forming a complex. Unbound antigens are then removed by washing. After addition of Streptavidin HRP conjugate, it binds with biotinylated antigen and forming complex with HRP conjugate. After addition of the TMB substrate, the presence of the conjugate complex is shown by development of a blue color resulting from a reaction between the enzyme and substrate. This reaction is then quenched by addition of the Stop Solution, and the absorbance value for each microwell is determined using a spectrophotometer at 450/620-690 nm.
Accuracy of Detection :
A total of 262 patient specimens were collected from susceptible subjects and tested by Dengue IgG ELISA Kit and by a commercial leading brand EIA.
Product Details:
Number of Reactions(Preps)/Kit : 96 Wells
Brand : CTK BioTech
Sample : Serum / Plasma
Storage : 2-8 C
Cat No : AE0315
The TRUSTwell CHIK IgM Test is a solid phase enzyme linked immunoabsorbent assay for the qualitative detection of IgM anti- Chikungunya virus in human serum or plasma. It is intended for professional use only as an aid in the diagnosis of acute infection with Chikungunya viruses. Any reactive specimen with the TRUSTwell CHIK IgM Test must be confirmed with alternative testing method(s) and clinical findings.
TEST PRINCIPLE:
TRUSTwell CHIK IgM Test is a solid phase enzyme linked immunoabsorbent assay based on the principle of the indirect immunoassay technique for the detection of IgM anti- Chikungunya virus in human serum or plasma. The TRUSTwell CHIK IgM Test is composed of two key components: 1) Solid microwells pre-coated with recombinant CHIK antigen(s); 2) Liquid conjugates composed of monoclonal anti-human IgM reagent conjugated with horse reddish peroxidase (HRP-anti-Human IgM conjugates). During the assay, the test specimen is first incubated with the coated microwells. IgM anti- Chikungunya virus, if present in the specimen, binds to the antigen coated on the microwell surface.
In the second incubation with the HRP-anti Human IgM conjugates, the IgM antiChikungunya antibody absorbed on the surface of microwell reacts to the conjugates, forming a complexed conjugates. Unbounded conjugates are then removed by washing. The presence of the complexed conjugates is shown by a blue color upon additional incubation with TMB substrate. The reaction is stopped with Stop Solution and absorbances are read using a spectrophotometer at 450 /620-690 nm.
Clinical Performance:
A total of 336 specimens from susceptible subjects were tested by TRUSTwell CHIK IgM and by a commercial reference ELISA kits.
Product Details:
Number of Reactions(Preps)/Kit : 96 Wells
Brand : Abbott
Cat. No : 01PE40
Panbio Dengue Early ELISA is a dengue NS1 antigen capture ELISA. It is used to detect NS1 antigen in serum as an aid to clinical laboratory diagnosis of patients with clinical symptoms consistent with dengue fever. The Dengue Early ELISA should be used in conjunction with other dengue serological assays.
Number of Reactions(Preps)/Kit : 96wells
Brand : Abbott
Cat. No : 01PE10
The Panbio Dengue IgG Capture ELISA is used to detect elevated IgG antibodies to dengue virus (serotypes 1-4) in patients with secondary infection. This test is intended as an aid in the clinical laboratory diagnosis.
Number of Reactions(Preps)/Kit : 96 Wells
Brand : InBios
Sample Material : Serum
Incubation Time: 60+60+60+5+10+1
Storage 2-8 C
Cat No : DDMS-1
The DENV DetectTM IgM Capture ELISA is for the qualitative detection of IgM antibodies to DENV recombinant antigens in serum for the presumptive clinical laboratory diagnosis of Dengue virus infection. The assay is intended for use only in patients with clinical symptoms consistent with either dengue fever or dengue hemorrhagic fever.
The complete kit includes one 96 well strippable plate with all necessary reagents and controls.
1st Assay to Receive FDA Clearance.
Performance thoroughly evaluated with clinically confirmed cases of dengue 1-4 serotypes.
Excellent positive and negative agreement with WHO reference panel (>90%).
Improves accuracy by monitoring background reactivity with a normal cell antigen.
Employs a simple, one step ratio method of interpretation.
CE Marked.
Number of Reactions(Preps)/Kit ; 96 wells
Brand : Abbott
Test Type : Elisa
CAT No : E-LEP01M / E-LEP01M05
The Panbio Leptospira IgM ELISA is for the qualitative detection of IgM antibodies to leptospira in serum as an aid in the clinical laboratory diagnosis of patients with clinical symptoms consistent with leptospirosis.
Number of Reactions(Preps)/Kit : 96 wells
Brand : Abbott
Usage/Application : Hospital
Sample Material : Serum
CAT No : 11EK10
The Panbio Dengue IgM Capture ELISA is used to detect IgM antibodies to dengue antigen in serum as an aid to clinical laboratory diagnosis of patients with clinical symptoms consistent with dengue fever. The Panbio. Dengue IgM Capture ELISA should be used in conjunction with other dengue serology.
Number of Reactions(Preps)/Kit : 100
Brand : Siemens
The Multistix 10 SG reagent strip is the reliable frontline test for detection of a broad range of conditions, from detecting urinary tract infections (UTI1) to diabetes and kidney disorders. Accurately gain a broader clinical insight into a patient's health.
Usage/Application Hospital
Country of Origin Made in India
The Afinion Lipid Panel test and the fully automated Afinion Analyzer, give you reliable results conveniently available when and where you need them. Patient consultations can be carried out with confidence.
Test for quantitative determination of Total Cholesterol, High-Density Lipoprotein (HDL) cholesterol, Low- Density Lipoprotein (LDL) cholesterol, Triglycerides (Trig), non-HDL and Chol/HDL ratio in whole blood, serum and plasma to be used in the diagnosis and treatment of lipid disorders.
BENEFITS:
Test for the quantitative determination of:
THE IMPORTANCE OF MEASURING A LIPID PANEL
Elevated cholesterol is one of the major risk factors for coronary heart disease, heart attack and stroke. As the blood cholesterol rises, so does the cardiovascular disease risk. Many patients such as those with metabolic syndrome have comorbid conditions such as high lipids and diabetes. And if other risk factors are present such as smoking, high blood pressure or diabetes, the risk increases even further.
Measuring a Lipid Panel/Cholesterol is recommended by NCEP (National Cholesterol Education Program) every five years in healthy adults, more regularly if you have other risk factors, in children and youths who are at an increased risk and to evaluate the success of lipid-lowering treatment.
See how POC diabetes testing significantly impacts patient care with better glycemic control, increased compliance, and improved office efficiencies. Read the presentation or download the PowerPoint for your own use.
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