Product Details:
Number of Reactions(Preps)/Kit 40T
Brand ; SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 15min
CAT No : RK025-40
One step, rapid immunothematographic test for the differential detection between Plasmodium falciparum Histidine- Rich Protein II (HRP II) and Plasmodium species (P. falciparum , P vivax P. ovale, P. malariae) lactate dehydrogenase (pLDH) in human whole blood
Kit Contents:
Standard Q Malaria Pf/PV Ag cassette x 40
Specimen transfer device 3 microlitre x 40
Butter bottle 3m1 x 02
Instructions for use x 01
STANDARD Q Malaria P.f Ag qualitatively analyzes Plasmodium falciparum and Plasmodium vivax antigens in whole blood using immunochromatography. The target antigen is Histidine-Rich Protein II (HRP-II) of Plasmodium faciparum and plasmodium lactate dehydrogenase (pLDH) of Plasmadium vivax, and the screening test result can be obtained within 15 minutes with its high sensitivity and specificity
Advantage:
Distinguish the infection between P.falciparum and P.vivax
Optimized on-site diagnosis with the small diagnostic kit
Able to read positive/negative infections fast and accurately with a little blood (5aul)
Room temperature storage.
Number of Reactions(Preps)/Kit : 40T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 15 min
CAT No : RK027-40
STANDARD Q Malaria P.f Ag qualitatively analyzes Plasmodium falciparum and Plasmodium species antigens in whole blood using immunochromatography. The target antigen is Histidine-Rich Protein II (HRP-II) of Plasmodium faciparum and plasmodium lactate dehydrogenase (pLDH) of Plasmadium species, and the screening test result can be obtained within 15 minutes with its high sensitivity and specificity.
Distinguish the infection between P.falciparum and others
Optimized on-site diagnosis with the small diagnostic kit
Able to read positive/negative infections fast and accurately with a little blood (5aul)
Room temperature storage
Number of Reactions(Preps)/Kit: 30T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits): 10 min
Country of Origin : Made in India
CAT No : RK026-30
STANDARD Q HBsAg performs qualitative analysis by specifically detecting the surface protein antigens of hepatitis B virus in serum, plasma and whole blood using immunochromatography. With a simple test method, hepatitis B infection can be discriminated early, and with its high sensitivity and specificity, the screening test result can be obtained within 20 minutes.
Easy to use, Easy to read and interpret
Room temperature storage
Performance
Sensitivity : 100% (43/43) / Specificity : 100% (162/162)
Product Details:
Number of Reactions(Preps)/Kit : 20T
Brand ; SD Biosensor
ICMR Approved ; Yes
Result Time (Rapid Kits) : 15 min
CAT No : RK029-20
STANDARD Q TSUTSUGAMUSHI IgM/IgG is a rapid,sensitive,qualitative Immunochromatographic assay for the detection of IgM/IgG antibodies against Orientia Tsutsugamushi in human serum,Plasma or whole blood specimen.it is an initial screening test and this test kit is for in vitro use only by professionals.
Differential detection of IgM & IgG Antibodies
Easy to use,Easy to interpret
Long term storage
Faster results with lesser specimen volume (10aul)
Product Details:
Number of Reactions(Preps)/Kit : 20T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 15 min
CAT No : RK024-20
STANDARD Q Chikungunya IgM/IgG qualitatively analyzes IgM and IgG antibodies specific to Chikungunya virus in serum, plasma and whole blood using immunochromatography. Screening test results can be obtained within 15 minutes with high sensitivity and specificity.
Differential detection of IgG and IgM antibodies
Easy to use, Easy to read and interpret
Room temperature storage
Able to read positive/negative infections fast and accurately with a little amount of sample (10 aul)
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Product Details:
Number of Reactions(Preps)/Kit : 30T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 15 min
CAT No : RK018-30
STANDARD Q HCV Ab qualitatively analyzes antibodies specific to hepatitis C virus in serum, plasma and whole blood using immunochromatography. With a simple test method, hepatitis C infection can be discriminated early, and with its high sensitivity and specificity, the screening test result can be obtained within 5 minutes.
Easy to use, Easy to read and interpret
Room temperature storage
Performance
Sensitivity : 98.9% (92/93) / Specificity : 100% (168/168)
Number of Reactions(Preps)/Kit : 50T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 10 min
CAT No : RK022-50
"STANDARD QA Ultra-DotA HIV Test is a rapid, sensitive andqualitative immunochromatographic assay to detect circulatingantibodies against HIV in human serum or plasma. The test is for invitro diagnostic use and is intended as an aid to early diagnosis ofHIV infection. This test is intended for professional use only as aninitial screening test."
Number of Reactions(Preps)/Kit : 50
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 10 min
CAT No : RK023-50
STANDARD QA Ultra-DotA HCV Test is a rapid, sensitive andqualitative immunochromatographic assay to detect antibodiesagainst HCV in human serum or plasma. This test is for in vitrodiagnostic use and intended as an aid to early diagnosis of HCVinfection in patient with clinical symptoms with HCV infection.The test provides an initial screening result only. More specificalternative diagnosis methods should be performed in order toobtain the confirmation of HCV infection.
Product Details:
Brand : Boditech Med Incorporated
Size : 25 T
Samples : Human serum/plasma/ control
Specimen volume : 75 Microliter
stored at ; 4 - 30 DegreeC
Cat No ; CFPC-44
T3
Assessing to diagnosis & to monitor thyroid diseases(T3)
This test assesses the level of T3 in the blood to diagnose thyroid dysfunction, help to receive appropriate treatment, and help to confirm the treatment effect through periodic measurement.
INTENDED USE :
ichroma T3 is a fluorescence Immunoassay (FIA) for the
quantitative determination of triiodothyronine (total T3) in
human serum/plasma. It is useful as an aid in management
and monitoring of determination of thyroid disorders.
For in vitro diagnostic use only.
PRINCIPLE :
The test uses a competitive immunodetection method.
In this method, the analyte in the sample binds to the
fluorescence labeled (FL) detection antibody in detection
buffer, to form the complex as sample mixture. This complex
is loaded to migrate onto the nitrocellulose matrix, where
the covalent couple of T3 and bovine serum albumin (BSA) is immobilized and interferes with the binding of analyte and fluorescence labeled (FL) antibody. If more analytes exist in the sample, less detection antibodies are accumulated,
resulting in less fluorescence signal.
Product Details:
Brand : Boditech Med Incorporated
Size : 25 T
Specimen : Human serum/plasma/ control
Specimen volume : 75 microliter
stored at 4 - 30 DegreeC.
Cat No : CFPC-26
T4
Assessing to diagnosis & to monitor thyroid diseases(T4)
Thyroxine (T4) is a type of thyroid hormone. An abnormal amount of T4 may indicate thyroid disease. The T4 test measures total T4, including T4 bonded to protein and free T4. A T4 test will help determine what type of problem is affecting the thyroid.
INTENDED USE :
ichroma T4 is a fluorescence Immunoassay (FIA) for the quantitative determination of thyroxine (T4) in human serum/plasma. It is useful as an aid in management and monitoring of thyroid disorder.
For in vitro diagnostic use only.
PRINCIPLE :
The test uses a competitive immunodetection method.
In this method, the target material in the sample binds to the fluorescence (FL)-labeled detection antibody in detector, to form the complex as sample mixture. This complex is loaded to migrate onto the nitrocellulose matrix, where the covalent couple of T4 and bovine serum albumin (BSA) is immobilized on a test strip, and interferes with the binding of target material and FL-labeled antibody. If the more target material exists in blood, the less detection antibody is accumulated, resulting in the less fluorescence signal.
Product Details:
Brand ; Boditech Med Incorporated
Size : 25 T
Samples: human whole blood/serum /plasma
Specimen volume human whole blood/serum/ plasma
stored at 4-30 C
Cat. No. : CFPC-66
Human Chorionic Gonadotropin (�²-hCG)
Distinguish pregnancy and abnormal pregnancy
The IhCG test can be used to confirm pregnancy, the age of the fetus, abnormal pregnancy (ectopic pregnancy), potential miscarriage, and down syndrome.
INTENDED USE :
ichroma -HCG Plus is a fluorescence Immunoassay (FIA) for the
quantitative determination of -HCG in human whole blood/serum
/plasma. It is useful as an aid in management and monitoring of beta
human chorionic gonadotropin (hCG) level in human
For in vitro diagnostic use only.
PRINCIPLE :
The test uses a sandwich immunodetection method; Dried
antibodies in the detector tube, once diluted with the diluent, bind
with antigens in the sample to form antigen-antibody complexes.
These complexes then migrate through the nitrocellulose matrix and
are captured by another sets of immobilized antibodies on the test line.
The more antigens in the sample, the more antigen-antibody
complexes, which leads to a stronger fluorescence signal. This signal
then is interpreted by the reader to display the �²-HCG concentration in
the sample.
STORAGE AND STABILITY :
The cartridge is stable for 20 months (while sealed in the original
aluminum foil pouch) if stored at 4-30 C.
The detector, diluent and sample diluent are stable for 20 months
if stored at 2-8 C.
After the cartridge pouch is opened, the test should be
Product Details:
Brand: Boditech Med Incorporated
Size : 25 T
Samples : human serum/plasma
Specimen volume : 150 Microliter
stored at 4 - 30 DegreeC.
Cat. No : CFPC-22
Thyroid Stimulating Hormone (TSH)
Diagnosing thyroid dysfunction
One needs an adequate level of thyroid hormone. The excessive or insufficient level would cause various abnormalities in human physiology. The TSH test can deliver the required answer about the hormone level in 12 minutes with fingertip blood (US FDA 510k; AFIAS TSH).
INTENDED USE :
ichroma NT-proBNP is a fluorescence Immunoassay (FIA) for the quantitative determination of NT-proBNP in human whole blood/serum/plasma. It is useful as an aid in the diagnosis of persons suspected of having congestive heart failure.
For in vitro diagnostic use only.
PRINCIPLE :
The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigens in the sample, forming antigen-antibody complexes, and migrate onto the nitrocellulose matrix to be captured by the other immobilized-antibodies on test strip.
More antigens in the sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by instrument for ichromaâ?¢ tests to show NT-proBNP concentration in the sample.
Product Details:
Brand : Boditech Med Incorporated
Size : 25 Test
Samples : Whole blood
Sample volume : 75 Microliter
Cat No : CFPC-38
Storage Temperature ; 4 - 30 DegreeC
HbA1c
Assessing the level of glycated hemoglobin in the blood
This test is certified by NGSP (National Glycohemoglobin Standardization Program). It helps diabetic diagnosis, treatment, and prognosis by measuring the glycated hemoglobin concentration (%) in a small amount of blood over the past 3 months.
INTENDED USE
ichroma HbA1c is a fluorescence Immunoassay (FIA) for the quantitative determination of HbA1c(Hemoglobin A1c) in human whole blood. It is useful as an aid in management and monitoring of the longterm glycemic status in patients with diabetes mellitus. For in vitro diagnostic use only.
PRINCIPLE:
The test uses a sandwich immunodetection method; the detector antibody in buffer binds to antigen in sample, forming antigen-antibody complexes, and migrates onto nitrocellulose matrix to be captured by the other immobilized-antibody on test strip. The more antigen in sample forms the more antigen-antibody complex and leads to stronger intensity of fluorescence signal on detector antibody. Instrument for ichromaâ?¢ tests displays the content of glycated hemoglobin in terms of percent of the total hemoglobin in blood.
Product Details:
Brand : Boditech Med Incorporated
Size : 25 T
Samples : whole blood/serum/plasma
Sample volume : 75 Microliter
stored at 4 - 30 DegreeC
Cat No i CHROMA PSA-25
Prostate Specific Antigen (PSA)
Screening for the prostate cancer & monitoring the effects of the treatment
This test helps in the early detection of prostate diseases such as enlarged prostate and prostatitis and prostate cancer by quantifying PSA in male blood, as well as observation of treatment effects and monitoring of recurrence.
Product Details:
Brand ; Boditech Med Incorporated
Size : 25 Test
Samples : Serum/Plasma
Recommended anticoagulant K2 EDTA, K3 EDTA, sodium heparin
Storage Temperature : 4 - 30 DegreeC
Cat No : CFPC-21
Progesterone
Monitoring ovulation abnormalities and predicting miscarriage & ectopic pregnancy
The progesterone test kit measures the level of progesterone in the blood. The progesterone test alone is not enough to diagnose a particular problem. But the result may help provide answers to causes of infertility, risk of miscarriage, ovulation, and ectopic pregnancy.
PRINCIPLE :
The test uses a competitive immunodetection method. In this method, the analyte in the sample binds to the fluorescence labeled (FL) detection antibody in detection buffer, to form the complex as sample mixture. This complex is loaded to migrate onto the nitrocellulose matrix, where the covalent couple of progesterone and bovine serum albumin (BSA) is immobilized, and interferes with the binding of analyte and fluorescence labeled (FL) antibody. If more analytes exist in the sample, less detection antibodies are accumulated, resulting in less fluorescence signal.
Number of Reactions(Preps)/Kit : 30T
Brand : CTK BioTech
Result Time (Rapid Kits) : 15 min
Sample Type : Blood
Test Type : Rapid Test
CAT No : R0101C
Accuracy: 100% specificity and 100% sensitivity in comparison with a reference rapid test on the market
Cross Reactivity: No false positive results were observed on specimens from TP, HIV, Dengue, TB, Typhoid Ab , HBsAg, HCV Ab, HEV Ab, H.P Ab, HAV, HCG, RF, ANA, HAMA
Interference: No interference were seen with substances: Salicylic acid: 4.34 mmol/L; Glucose: 55 mmol/L; Sodium citrate: 3.8 %; Heparin: 3,000 U/L; Creatinine: 442 �¼mol/L; Bilirubin: 20 mg/dL; EDTA: 3.4 �¼mol/L; Hemoglobin: 2g/L; Human IgG: 1000 mg/dL; AlbuminL 60 g/L
Shelf life: 24 month
Individually sealed foil pouches containing:
One cassette device
One desiccant
5L capillary tubes
Sample diluent (REF SB-R0101, 5 mL/bottle)
One package insert (instruction for use)
Product Details:
Brand : Boditech Med Incorporated
Size : 25 T
Samples : Human serum/plasma/control
Specimen volume : 50 Microliter
stored at 4 - 30 DegreeC
Cat No : CFPC-89
INTENDED USE :
ichroma AMH is a fluorescence Immunoassay (FIA) for the quantitative determination of AMH (Anti-m�¼llerian hormone) in human serum/plasma. It is useful as an aid in management and monitoring of premature ovarian insufficiency, menopause and ovarian reserve.For in vitro diagnostic use only.
COMPONENTS :
ichroma AMH consists of cartridges, detectors and diluent The cartridge contains the membrane called a test strip which has streptavidin at the test line and chicken IgY at the control line. All cartridges are individually sealed in an aluminum foil pouch containing a desiccant in a box The detector has 2 granules containing anti human AMH-fluorescence conjugate, anti-chicken IgY-fluorescence conjugate, anti-human AMH-biotin conjugate, bovine serum albumin (BSA) and sucrose as a stabilizer, MAB33 as a blocker in Tris-HCl buffer. All detectors are packed in a box The diluent contains bovine serum albumin and NaCl as a stabilizer, tween 20 and CA-630 as a surfactant and sodium azide as a preservative in phosphate buffered saline (PBS), and it is pre-dispensed in a vial. The diluent is packed in a box.
PRINCIPLE :
The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigens in the sample, forming antigen-antibody complexes, and migrate onto nitrocellulose matrix to be captured by the other immobilized-antibody on test strip.More antigens in sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by instrument for ichroma tests to show human AMH concentration in the sample.
INTERPRETATION OF TEST RESULT :
The instrument for ichroma tests calculates the test result automatically and displays AMH concentration of the test sample in terms of ng/mL The working range: 0.02- 15 ng/mL
Product Details:
Number of Reactions(Preps)/Kit : 25 T
Brand : Boditech Med Incorporated
Sample Volume : 30 Microliter
Sample : human serum / plasma / control
Reaction Time ; 10 mins
Cat No : CFPC-32
Ferritin
Monitoring deficiency/excess of iron & inflammation
Ferritin is a universal intracellular protein that stores iron and releases it in a controlled fashion. Too little ferritin can lead to anemia, while too much to liver disease, rheumatoid arthritis, other inflammatory conditions, or hyperthyroidism. The ferritin test measures the level of ferritin in the blood.
INTENDED USE :
ichromaâ?¢ Ferritin is a fluorescence Immunoassay (FIA) for the quantitative determination of Ferritin in human serum/plasma. It is useful as an aid for quantifying human ferritin.
For in vitro diagnostic use only.
PRINCIPLE :
The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigen in the sample, forming antigen-antibody complexes, and migrates onto nitrocellulose matrix to be captured by the other immobilized-antibodies on test strip.
More antigens in the sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by Instrument for ichrom tests to show ferritin concentration in sample.
Product Details:
Number of Reactions(Preps)/Kit : 25 T
Brand : Boditech Med Incorporated
Sample : whole blood (AFIAS), plasma, serum
Reaction Time : 15mins
Detection Range : ichroma(TM) (1 - 100 mIU/ml)
Cat No : CEPC-35
Follicle-stimulating Hormone (FSH)
Diagnosis of early menopause & ovarian degeneration and infertility
This test can help figure out the cause of infertility, problems with ovarian functions, menstrual abnormalities and congenital or acquired gonadotropin development disorder or infertility.
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