Raj Biosis Private Limited

STANDARD Q Ebola Zaire Ag Test is an immunoassay that can identify the presence of Ebola Zaire virus antigens in respiratory specimens, and displays the result in a qualitative way. STANDARD Q Ebola Zaire Ag Test helps with diagnostic and treatment decision for patients in clinical setting.

Advantage

• Easy to use, Easy to read and interpret
• Room temperature storage
• Suitable for Point of Care Testing
• No need for extra equipment

STANDARD Q Chikungunya IgM/IgG Test 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.

Advantage

• Differential detection of IgG and IgM antibodies
• Easy to use, Easy to read and interpret
• Room temperature storage of 2-40℃ / 36-104℉
• Able to read positive/negative infections fast and accurately with a little amount of sample (10 µl)

STANDARD Q TB MPT64 Ag performs qualitative analysis by detecting Mycobacterium tuberculosis (TB) MPT64 antigen in solid culture or liquid culture samples using immunochromatography. With a simple test method, the screening test result can be obtained within 10 minutes with its high sensitivity and specificity.

Advantage

• Easy to use, Easy to read and interpret
• Room temperature storage at 2-40°C/36-104°F

STANDARD Q Zika IgM Test qualitatively analyzes IgM antibodies specific to Zika virus in serum, plasma and whole blood using immunochromatography. Screening test results can be obtained within 15 minutes with high sensitivity and specificity.

Advantage

• Differential detection of 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 µl)

An immunochromatographic assay for the detection of IgM to Zika/Dengue/Chikungunya/Yellow fever virus and Dengue NS1 Ag.

STANDARD Q Arbo Panel I (Z/D/C/Y) test is an immunochromatographic assay for the detection of IgM to Zika or Dengue or Chikungunya or Yellow fever virus and Dengue NS1 antigen in human serum, plasma or whole blood. Screening test results can be obtained within 15 minutes with high sensitivity and specificity.

Advantage

• Detect Zika/Dengue/Chikungunya/Yellow fever virus IgM and Dengue NS1 Ag simultaneously at once
• Easy to use, Easy to read and interpret
• Room temperature storage of 2-40℃ / 36-104℉

 Luteinizing Hormone (LH) Assessing and monitoring function of pituitary gland This test helps evaluate pituitary function by quantifying luteinizing hormone in the blood, to diagnose pituitary gland disease, and to determine congenitally or acquired gonadotropin dysfunction.

STANDARD Q Yellow Fever IgM Test qualitatively analyzes IgM antibodies specific to Yellow Fever virus in serum, plasma and whole blood using immunochromatography. Screening test results can be obtained within 15 minutes with high sensitivity and specificity.

Advantage

• Differential detection of IgM antibodies
• Easy to use, Easy to read and interpret
• Room temperature storage of 2-40℃ / 36-104℉
• Able to read positive/negative infections fast and accurately with a little amount of sample (10 µl)

STANDARD Q Strep A Ag performs qualitative analysis by detecting Group A streptococcal antigens using immunochromatography. With a simple test method, presence/absence of infection can be discriminated, and with its high sensitivity and specificity, the screening test result can be obtained within 5 minutes.

Advantage

• Easy to use, Easy to read and interpret
• Support
• Room temperature storage

STANDARD Q RSV Ag Test is a rapid chromatographic immunoassay for the qualitative detection of RSV antigen present in nasopharyngeal secretion from patients with symptoms of a viral respiratory infection. This test is for in vitro professional diagnostic use and intended as an aid to early diagnosis of RSV infection. It provides only an initial screening test result. Specific alternative diagnosis method should be performed in order to obtain the confirmation of RSV infection.

Advantage

• Getting a fast result in 15-30 minutes
• Easy handling which does not require specific training
• Suitable for Point Of Care Testing
• No follow-ups or equipments required
• Video guide provided (soon)
• External quality controls provided

This product performs qualitative analysis on Dengue virus-specific IgM and IgG antibodies in serum, plasma and whole blood.

Advantage

• Getting fast results In 15 ~ 20 minutes
• Wide storage range of 2~40℃ (36~104℉)
• Easy and convenient testing process Suitable for Point of Care Testing
• No need for using extra equipment

STANDARD Q Adeno Respi Ag Test is an immunoassay that can identify the presence of Adenovirus antigens in respiratory specimens, and displays the result in a qualitative way. STANDARD Q Adeno Respi Ag Test helps with diagnostic and treatment decision for patients in clinical setting.

Advantage

• Easy to use, Easy to read and interpret
• Room temperature storage
• No need for extra equipment

This product performs qualitative analysis on NS1 antigens of Dengue virus and Dengue virus specific IgM/IgG in serum, plasma and whole blood.

STANDARD Q Dengue Duo test is an immunochromatographic assay for the detection of NS1 antigen and Dengue virus-specific IgM and IgG antibodies in human serum, plasma and whole blood. By detecting the NS1 antigen, not only the initial infection can be detected, but also Dengue virus-specific IgM and IgG can be detected at the same time. Screening test results can be obtained within 15 minutes with high sensitivity and specificity.

Advantage

• Getting fast results In 15 ~ 20 minutes
• Wide storage range of 2~40℃ (36~104℉)
• Effective in detecting the antigen(NS1 protein) and antibody(IgM/IgG)
• Suitable for Point of Care Testing
• No need for using extra equipment

This product performs qualitative analysis on NS1 antigens of Dengue virus in serum, plasma and whole blood.

Advantage

• Getting fast results In 15 ~ 20 minutes
• Wide storage range of 2~40℃ (36~104℉)
• Easy and convenient testing process
• Effective in detecting the antigen(NS1 protein)
• Suitable for Point of Care Testing
• No need for using extra equipment

STANDARD Q Filariasis Ag Test is a rapid chromatographic immunoassay for the qualitative detection of Wuchereria bancrofti antigens present in human blood.
STANDARD Q Filariasis Ag Test is an immunochromatographic assay for the detection of Wuchereria bancrofti antigens in human serum, plasma, or whole blood specimens. This test kit is for in vitro diagnostics use only. This is intended for professional use, only for an initial screening test.

Advantage

• Getting results In 10 ~ 20 minutes
• Optimized on-site diagnosis with small diagnostic kit
• Wide storage temprature at 2-40°C / 36-104°F
• Suitable for Point of Care Testing
• No need for extra equipment

STANDARD Q H. pylori Ab Test performs qualitative analysis by detecting antibodies specific to Helicobacter pylori in serum, plasma and whole blood using immunochromatography. With a simple test method, With its high sensitivity and specificity, the screening test result can be obtained within 10 minutes.

Advantage

• Easy to use, Easy to read and interpret
• Room temperature storage at 2-40°C/36-104°F

STANDARD Q Tsutsugamushi IgM/IgG qualitatively analyzes IgM and IgG antibodies specific to Orienta tsutsugumushi in serum, plasma and whole blood using immunochromatography. Screening test results can be obtained within 15 minutes with high sensitivity and specificity.

Advantage

• Differential detection of IgG and IgM antibodies
• Easy to use, Easy to read and interpret
• Room temperature storage of 2-40℃ / 36-104℉
• Able to read positive/negative infections fast and accurately with a little amount of sample (10 µl)

STANDARD Q Leptospira IgM/IgG qualitatively analyzes IgM and IgG antibodies specific to Leptospira interrogans in serum, plasma and whole blood using immunochromatography. Screening test results can be obtained within 15 minutes with high sensitivity and specificity.

Advantage

• Differential detection of IgG and IgM antibodies
• Easy to use, Easy to read and interpret
• Room temperature storage of 2-40℃ / 36-104℉
• Able to read positive/negative infections fast and accurately with a little amount of sample (10 µl)

STANDARD Q Influenza A&B Test performs qualitative analysis by detecting influenza virus A type and B type antigens in human nasopharynx.

Advantage

• Getting a fast result in 8-12 minutes
• Easy handling which does not require specific training
• Suitable for Point Of Care Testing
• No follow-ups or equipments required
• Video guide provided (soon)

STANDARD Q H.pylori Ag Test is an immunochromatographic assay for the detection of Helicobacter pylori antigen in the human stool sample. Users can easily and rapidly get the accurate result of the test within 10 minutes. Advantage  Easy to use, read, and interpret Room temperature storage 

STANDARD Q Syphilis Ab performs qualitative analysis by detecting antibodies specific to Treponema pallidum in serum, plasma and whole blood using immunochromatography. With a simple test method, Syphilis infection can be discriminated, and with its high sensitivity and specificity, the screening test result can be obtained within 5 minutes.

Advantage

• Easy to use, Easy to read and interpret
• Room temperature storage

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.

STANDARD Q HBsAg Test is a rapid chromatographic immunoassay for the qualitative detection of Hepatitis B surface antigen (HBsAg) present in serum or plasma specimen. This test is for in vitro professional diagnostic use and intended as an aid to early diagnosis of HBV infection in patient with clinical symptoms with HBV infection. It provides only an initial screening test result. More specific alternative diagnosis methods should be performed in order to obtain the confirmation of HBV infection.

Advantage

• Easy to use, Easy to read and interpret
• Room temperature storage

STANDARD Q HAV IgM Test is an immunochromatographic assay for the detection of hepatitis A virus IgM antibody in human serum, plasma or whole blood sample. This test kit is for in vitro use only. This is intended for professional use, only for an initial screening test.

Advantage

• Easy to use, read, and interpret
• Room temperature storage at 2-40°C/36-104°F

STANDARD™ Q HIV 1/2 Ab 3-Line Test is a rapid chromatographic immunoassay for the qualitative detection of antibodies specific to HIV-1 including subtype O and HIV 2 in human serum, plasma or venous and capillary whole blood. The test is for in vitro diagnostic use and intended as an aid to diagnosis of HIV in symptomatic, asymptomatic populations and persons at risk of HIV infection.

Advantage

• Getting a fast result in 10-20 minutes
• Easy handling which does not require specific training
• Suitable for Point Of Care Testing
• No follow-ups or equipments required
• Discrimination between HIV-1 and HIV-2 antibodies

STANDARD Q HIV/Syphilis Combo performs qualitative analysis by detecting antibodies specific to HIV-1, HIV-2 and Syphilis (Treponema pallidum) in serum, plasma and whole blood using immunochromatography. With a simple test method, HIV and/or syphilis infection status can be discriminated, and with its high sensitivity and specificity, the screening test result can be obtained within 15 minutes.

Advantage

• Simultaneous detection of HIV-1/2 and Syphilis in one test
• Easy to use, Easy to read and interpret
• Discrimination between HIV-1 and HIV-2 antibodies
• Room temperature storage

STANDARD Q TnI Test is an immunochromatographic assay for the detection of cardiac Troponin I (cTnI) levels in human
serum, plasma (EDTA), or whole blood (EDTA) samples. This test is for in vitro and professional use only, and is only for an
initial screening test.

Advantage

• Room temperature storage at 2-40°C/36-104°F
• Easy and convenient testing process for professionals
• Suitable for Point of Care Testing

STANDARD Q ZIKV/DENV/CHIKV Fast Quad Test is an immunochromatographic assay for the detection of Dengue IgM or Dengue NS1 or Zika IgM or Chikungunya IgM in human serum, plasma or whole blood. Screening test results can be obtained within 15 minutes with high sensitivity and specificity.

Advantage

• Detect Dengue IgM or Dengue NS1 or Zika IgM or Chikungunya IgM simultaneously at once
• Easy to use, Easy to read and interpret
• Room temperature storage of 2-40℃ / 36-104℉

STANDARD Q Zika / Dengue Trio Test is an immunochromatographic assay for the detection of IgM and IgG antibodies specific for Dengue virus and NS1 antigen as well as Zika virus specific IgM and IgG antibodies in human serum, plasma and whole blood. Screening test results can be obtained within 15 minutes with high sensitivity and specificity.

Advantage

• Detect Zika and Dengue simultaneously at once
• Easy to use, Easy to read and interpret
• Room temperature storage

STANDARD Q Malaria/CRP Duo Test is an immunochromatographic assay for the qualitative detection of P. falciparum specific to HRP-2, Plasmodium species (P. falciparum, vivax, ovale and malariae) specific to pLDH and C-Reactive Protein (CRP) in human whole blood specimen.

STANDARD Q Malaria/CRP Duo Test is an immunochromatographic assay for the qualitative detection of P. falciparum specific to HRP-2, Plasmodium species (P. falciparum, vivax, ovale and malariae) specific to pLDH and C-Reactive Protein (CRP) in human whole blood specimen. For the patient with fever who has Malaria tests negative, CRP test can be used to help differentiate bacterial infection from viral infections. The detection limit of CRP test is 20mg/L. With this results, healthcare provider can provide correct and fast treatment and avoid unnecessarily treating viral infections with antibiotics. This test kit is for in vitro use only. This is intended for professional use, only for an initial screening test.

Advantage

• Easy to use, read, and interpret
• Room temperature storage
• Suitable for Point of Care Testing
• No need for extra equipment

STANDARD Q Malaria P.f Ag Test is a product that qualitatively analyzes Plasmodium falciparum antigens in whole blood using immunochromatography. The target antigen is Histidine-Rich Protein II (HRP-II), and the screening test result can be obtained within 15 minutes with its high sensitivity and specificity.

Advantage

• Optimized on-site diagnosis with the small diagnostic kit
• Room temperature storage at 2-40°C/36-104°F
• Able to read positive/negative infections fast and accurately with a little blood (5µl)
• Suitable for Point of Care Testing
• No need for extra equipment

STANDARD Q Dengue/Chikungunya Trio test is an immunochromatographic assay for the detection of Dengue IgM/IgG or Dengue NS1 or Chikungunya IgM/ IgG in human serum, plasma or whole blood. Screening test results can be obtained within 15 minutes with high sensitivity and specificity

Advantage

• Detect Dengue IgM/IgG or Dengue NS1 or Chikungunya IgM/IgG simultaneously at once
• Easy to use, Easy to read and interpret
• Room temperature storage of 2-40℃ / 36-104℉

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.

Advantage

• 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 (5µl)
• Room temperature storage of 2-40°C / 36-104°F
• Suitable for Point of Care Testing
• No need for extra equipment

STANDARD Q Malaria P.f/P.v 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 (5µl)
• Room temperature storage of 2-40°C / 36-104°F

STANDARD F2400 is a Fluorescent immunoassay system that uses fluorescent bead as a detector.
Higher sensitivity than the existing RDTs could be provided through advanced fluorescent detection with an UV
LED energy source.

This fluorescence immunoassay device that can perform qualitative and quantitative analysis on infections, respiratory diseases and chronic diseases supports convenient user interface and LIS/HIS connectivity.

Advantage

• Fluorescent immunoassay system 24 tests at once
• Top class performance with fluorescent technology
• Ready-to-use reagents
• Random Access
• Automatic test device discarding

1. Inspect the functional status of adrenal glands [adrenal function]2. Indirectly observe the functional status of pituitary [hypertension type determination]

Anti-Müllerian hormone (AMH) is a hormone secreted by granule cells in the growing follicles of an organism's ovary, which play an important role in regulating follicle activity. Serum AMH assessment can reflect ovarian reserve capacity in an early stage: the higher the AMH level, the higher the ovarian reserve. AMH secretion is not affected by the female menstrual cycle, and therefore its assessment is flexible in time.

Triiodothyronine (T3) :

T3 test can effectively assess thyroid function:(1) diagnosis and early diagnosis of hyperthyroidism;(2) To evaluate the therapeutic effect of hyperthyroidism;(3) Diagnosis of hypothyroidism, course observation and curative effect diagnosis.

25OH-VD is a steroid that supports the mineralization of osteoid and some other vitamins, hormones and minerals.It plays an important role in the formation and maintenance of strong bones. Serum 25OH-VD level is currently the well-acknowledged golden standard for evaluating VD nutritional status. Based on the gross amount 25OH-VD in the serum, one can determine the VD nutritional status of a human body. Vitamin D is also related to immune regulation, cardiovascular diseases, hypertension, diabetes, chronic renal diseases, auto-immune diseases, inflammation and common tumors.

Human Cytomegalovirus (CMV) :

CMV is one kind of double-stranded DNA virus. Pregnant women of CMV primary or recurrent infections can cause neonatal intrauterine or perinatal infection, but the harm of primary infection is more serious to fetus than that of recurrence infection. Most congenital infected fetals shows symptom of mental retardation, visually impaired, hearing loss, especially giant cell inclusion body disease (CI, characterized by reticuloendothelial system and invaded the central nervous system), which will cause multiple systems, multiple organ damage to baby.

Quantitative determinationof NT-proBNP (N-terminal pro B-type natriuretic peptide) in human serum and plasma. Clinical informationand imaging procedures are used to diagnose left ventricular dysfunction. The significance of natriuretic peptides in the control of cardiovascular system function has been demonstrated. Initial studiesreveal that natriuretic peptides can be used for diagnostic clinical problems associated with left ventricular dysfunction. Thefollowing natriuretic peptides have been described: atrial natriuretic peptide (ANP), B-typenatriuretic peptide (BNP), and C-typenatriuretic peptide (CNP).

Rubella Virus (Rubella) :

Rubella is one kind of RNA viruses. During the first 6 months of pregnancy, if pregnant women are infected with Rubella virus, the virus can invade the fetus through the placenta, causing miscarriage and stillbirth, about 29% of the birth baby have "Congenital Rubella Syndrome" (CRS), birth weight less than 2.5 kg, stunted growth; with systemic organ damage, congenital heart disease, deformity, deafness, blindness and so on.