Raj Biosis Private Limited

This product is a blood assay that can help to diagnose human tuberculosis using IGRA (Interferon Gamma Releasing Assay) method.Advantage Sensitive and specific IGRA test Unlike the classic way of tuberculin test (TST), TB-Feron ELISA only needs one clinic visit Not affected by Bacille-Calmette Guerin (BCG) vaccinations

BeneSphera™ HCV ELISA kit is for the qualitative detection of antibodies to HCV from human serum and plasma.

• Use recombinant antigen, consisting of Core, NS3, NS4, NS5 Antigens
• Detects all subtypes of HCV
• Sensitive to detect low antibody titre
• Sensitivity: 100%
• Specificity: 99,3%

BeneSphera™ HCV Microwell ELISA (IHF) is an in vitro, enzyme immuno assay for the qualitative determination of antibodies to Hepatitis C Virus in human serum or plasma.

To evaluate specificity of the BeneSphera™ HCV a total of 1500 samples were tested. All these samples were collected from the normal donors. Out of 1500 samples, 10 samples were found to be positive with BeneSphera™ HCV . The specificity of the BeneSphera™ HCV was thus found to be 99,3%.

The sensitivity of the BeneSphera™ HCV against tested commercially available HCV panels and samples obtained from clinical sites.

To test reproducibility of BeneSphera™ HCV, three plates from three production batches each were randomly selected and tested against a Q.C. panel of HCV positive and negative samples.

BeneSphera™ HIV Advanced ELISA kit is a fourth-generation immunoassay for qualitative detection of P24 antigen and antibodies to HIV-1 and HIV-2.

• Simultenious detection of antigen and antibodies to HIV 1 and 2
• Window period: 2 to 4 weeks
• Easy detection compared to 3rd generation assay
• Sensitivity: 100%
• Specificity: 100% 

BeneSphera™ HIV Advance (Ag-Ab) (IHF) Microwell ELISA is an in vitro enzyme immunoassay for the qualitative determination of HIV-I p24 antigen and Antibodies to HIV-I and HIV-2 in human serum or plasma.

BeneSphera™ T4 ELISA Kit for the quantitative determination of T4 (thyroxine) Hormone from human serum and plasma.

• Assay time: 1 h 30 min
• Expected range: male- 4,4 to 10,8 µg/dl, female- 4,8 to 11,6 µg/dl
• Sensitivity: 0,4 µg/dl
• Specificity: no interference found, total of 131 samples found to have high degree of correlation with T4 calibrators provided

Enzyme Immunoassay for the quantitative determination of T4 Hormone concentration in human serum/plasma.

BeneSphera™ T3 ELISA kit for the quantitative determination of T3 (Triiodothyronine) Hormone from human serum and plasma.

• Assay time: 1 hour 30 min
• Expected range: 0,52 to 1,85 ng/ml
• Sensitivity: 0,04 ng/ml
• Specificity: no interference found, total of 162 samples found to have high degree of correlation with T3 calibrators provided
• Precision: very low coefficient of variation found in intra-assay and inter-assay reproducibility studies

Enzyme Immunoasaay for the quantitative determination of T3 Harmone concetraion in human serum/plasma. For invitro diagnostics use only.

BeneSphera™ TSH ELISA Kit for the quantitative determination of TSH (Thyroid Stimulating Hormone ) Hormone from human serum and plasma.

• Assay time: 1 h 30 min
• Expected range: 0,39 to 6,16 µIU/ml
• Sensitivity: 0,078 µIU/ml
• Specificity: no interference found, total of 170 samples found to have high degree of correlation with TSH calibrators provided
• Precision: very low coefficient of variation found in intra-assay and inter-assay reproducibility studies

Enzyme Immunoassay for the quantitative determination of TSH Hormone concentration in human serum/plasma

BeneSphera™ HbsAg ELISA kit is for the qualitative detection of Hepatitis B Surface Antigen from human serum and plasma.

• Sandwich, non-competitive, immunoassay with HRP as a marker enzyme
• Detects all major 10 serotypes
• Analytical Sensitivity: 0,2 IU/ml
• Diagnostic sensitivity: 100%
• Diagnostic specificity: 99,5%

BeneSphera™ HBsAg Microwell ELISA (IHF) is an in vitro enzyme immuno assay for the qualitative detection of hepatitis B surface Antigen in human serum or plasma.

This assay promises to be more sensitive, convenient and safer to use, and has advantage of short reaction time as well as easier detection of target materials.

Product Information

Anti-Müllerian hormone (AMH), a member of the TGFβ superfamily, is a homodimeric glycoprotein composed of two 55 kDa N-terminal and two 12.5 kDa C-terminal homodimers, non-covalently linked by disulfide bridges.1

Recent studies have shown that the AMH C-terminal homodimer is much less active than the noncovalent complex, but almost all activity can be restored by associating with the N-terminal pro-region, which reforms a complex with the mature C-terminal homodimer. This finding raises the possibility that the AMH noncovalent complex is the active form of protein. 

STANDARD E Dengue NS1 Ag ELISA analyzes Dengue NS1 antigens in serum and plasma using enzyme linked immunosorbent assay. Advantage  Simple and easy to use: All necessary reagents included in the kit Highest accuracy with all dengue serotypes(DEN1,2,3, and 4) Able to detect antigens in samples with high sensitivity and specificity

Product Overview :-One Step qualitative immunochromatographic assay for detection of antibodies against HIV - 1 and HIV - 2 in human serum, plasma and whole blood (Fingerstick & Venous)

STANDARD E Malaria Ag ELISA analyzes Malaria antigens in whole blood using enzyme linked immunosorbent assay. Advantage Simple and easy to use: All necessary reagents included in the kit Able to detect antigens in samples with high sensitivity and specificity

STANDARD E Zika IgM ELISA analyzes IgM antibodies specific to Zika virus in serum and plasma using enzyme linked immunosorbent assay.
Advantage
Simple and easy to use - All necessary reagents included in the kit
High stability : 15 months at 2-8 °C

The TRUSTwell Malaria Ag ELISA Kit is a solid phase enzyme linked immunosorbent assay for the qualitative detection of malaria antigen in human blood sample.

Target: Pf HRP II and pLDH based detection
LOD: pLDH – 10 parasites/uL against WHO Standard pfHPRP-II – 20 parasites/uL against FIND Standard Specificity: No cross-reactivity with dengue, chikungunya & filarial infection
Precision: CV?10% Better sensitivity at 95% CI than competitors LOD is calibrated against WHO and FIND Standard96 well throughput suits blood donor screening Microwells coated with Anti-HRP II and Anti-pLDH monoclonal antibodiesPositive control Negative control Sample Diluent Enzyme conjugate (50 X concen trate) Conjugate Diluent Wash buffer (30 X concentrate) TMB substrat e (Ready to use) Stop solution ELISA Workin g Sheet Product insert DesiccantSealant.

HIV ELISA (3rd Generation)OSCAR 3rd Generation HIV 1 & HIV 2 ELISA is intended to be used for the detection of all subtypes (IgG, IgA, IgM) of antibodies to HIV 1 and HIV 2 viruses in human serum or plasma.

Pack Size: 96 Tests

The TRUSTwell Dengue IgM ELISA Kit is a solid-phase, IgM capture enzyme linked immunosorbent assay.

The three main kit components are:

1) A 96 breakable well plate with the solid microwells pre-coated with mouse monoclonal anti-human IgM antibody

2) Recombinant dengue antigen

3) HRP-anti-dengue conjugates

This test is intended to be used for the qualitative detection of IgM anti-dengue viruses (DEN1,2,3,4) in human serum or plasma. It is intended to be used by professionals as an aid in the diagnosis of acute dengue infection. Any interpretation or use of this test result must also rely on other clinical findings as well as on the professional judgment of healthcare providers.

Recommended For Use:Any person presenting with clinical signs or symptoms consistent with acute dengue infection or dengue fever including: high fever, severe headaches, pain behind the eyes, severe joint and muscle pain, fatigue, nausea, vomiting, and/or skin rash.During primary infection, anti-dengue IgM antibodies start to appear approximately 4-6 days after the onset of fever, peak at about 2 weeks, and remain in circulation for about 2-3 months. During secondary infection, IgM antibodies increase simultaneously with, or after the IgG antibody response, in general at a titer lower than IgG. Importantly, IgM antibody levels during secondary infection are significantly lower in comparison with primary infection.

HCV ELISA TestHCV ELISA is intended to be used for the detection of antibodies to HCV (Hepatitis C virus) in human serum or plasma.

For professional use only.

Pack Size: 96 Tests

The TRUSTwell HIV Ag-Ab ELISA Kit is a solid phase enzyme linked immunoabsorbent assay for the qualitative detection of HIV-1 P24 antigen, anti-HIV-1 including subtype O and anti-HIV-2 antibodies (including isotype IgG, IgM and IgA) in human serum or plasm. Based on double Ag/Ab-Sandwich immunoassay technique to ensure high specificity Solid microwells pre-coated with recombinant HIV-1, HIV-2 Ag and Anti-P24 Ab Liquid conjugates composed of recombinant HIV-1, HIV-2 Ag & SA conjugated with HRP Relative sensitivity: 100% and specificity: 99.9 % Comparable accuracy to the leading other ELISA kits Clear borderlines with high accuracy positive and negative controls Breakaway microwell strips Evaluated by NIB Assay time: 90 Minutes 12-months shelf life at 2-8 °C Microwells coated with anti-P24 Ab, recombinant HIV-1 and HIV-2 antigen Biotinylated P24 Ab HIV Ag positive control HIV Ag negative control HIV negative control HRP–avidin, HIV 1+2 conjugate mixture Sample diluent Wash buffer (30 x concentrate) TMB substrate A TMB substrate B Stop solution ELISA Working Sheet

The RBPL HAV IgM ELISA Test is a solid-phase enzyme-linked immunosorbent assay for the qualitative detection of IgM anti-hepatitis A virus in human serum or plasma.

• 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

• 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

STANDARD E Dengue IgG ELISA analyzes IgG antibodies specific to Dengue virus in serum and plasma using enzyme linked immunosorbent assay. Advantage Simple and easy to use - All necessary reagents included in the kit Highest accuracy with all dengue serotypes(DEN1,2,3, and 4)Able to detect antibodies in samples with high sensitivity and specificity

TRUSTwell Vitamin-D (Total) ELISA is a solid-phase enzyme-linked immunosorbent assay for the quantitative determination of Vitamin D (Vit D) level in human serum.
Accuracy: R2 = 0.918 with CLIA as reference.
Analytical Sensitivity: 1.2 ng/mL.
Specificity: No cross reactivity to non-hydroxylated vitamin D2 and Vitamin D3.
Intra & Inter assay precision: CV <=10%.
Higher linearity: 0-150 ng/mL.1 step less procedure, faster resulting. High & Low level assay controls included.
Accuracy: R2 = 0.918 with CLIA as reference.Analytical Sensitivity: 1.2 ng/mL.Specificity: No cross reactivity to non-hydroxylated vitamin D2 and Vitamin D3.Intra & Inter assay precision: CV <=10%.Higher linearity: 0-150 ng/mL.1 step less procedure, faster resulting.  High & Low level assay controls included.

The TRUSTwell Dengue IgG ELISA Kit is a solid-phase, IgG capture enzyme linked immunosorbent assay. The three main kit components are:

1) A 96 breakable well plate with the solid microwells pre-coated with mouse monoclonal anti-human IgG antibody

2) Recombinant dengue antigen

3) HRP-anti-dengue conjugates

This test is intended to be used for the qualitative detection of IgG anti-dengue viruses (DEN1,2,3,4) in human serum or plasma. It is intended to be used by professionals as an aid in the diagnosis of active infection with dengue viruses, including secondary infection. Any interpretation or use of this test result must also rely on other clinical findings as well as on the professional judgment of health care providers.

Recommended For Use:

Any person presenting with clinical signs or symptoms consistent with acute dengue infection or dengue fever including: high fever, severe headaches, pain behind the eyes, severe joint and muscle pain, fatigue, nausea, vomiting, and/or skin rash.

During primary infection, anti-dengue IgG antibodies become detectable by the end of the first week of illness. They increase slowly to peak around 14-21 days, and then decrease to low levels, persisting for the duration of life. During secondary infection, a strong and rapid IgG antibody response is often observed. IgG levels are detectable as early as 3 days after the onset of symptoms, with the peak detection window being 1-2 weeks after symptom onset. In secondary infection, IgG antibodies rise to levels higher than during primary infection. Importantly, anti-dengue IgG antibodies increase earlier than or simultaneously with IgM antibodies, and at much higher levels during secondary infection.

TRUSTwell Anti-Mullerian hormone (AMH) ELISA is a solid-phase enzyme-linked immunosorbent assay for the quantitative determination of AMH concentration in human serum or plasma. Accuracy: R2 = 0.96 (with Siemens CLIA)Analytical Sensitivity: 0.023ng/mL Specificity: No-cross reactivity with other fertility hormones Linearity: 0 - 14ng/mLIntra & Inter assay precision: CV <=10% User friendly package: 48 Test / Kiteady to use calibrators (6 level) & controls (2 level)

The TRUSTwell Dengue Ag (NS1) ELISA Kit is a solid-phase, enzyme linked immunosorbent assay that was developed using the antibody sandwich technique.
 
The two main kit components are:

1) A 96 breakable well plate with the solid microwells pre-coated with rabbit anti- Pan Dengue NS1 antibody
2) A conjugate solution composed of antibodies against Dengue NS1 antigen conjugated with horseradish peroxidase (HRP-anti-dengue NS1 conjugates) This test is intended for the qualitative detection of dengue NS1 antigen (DEN1, 2, 3, 4) in human serum or plasma. It is intended to be used by professionals as an aid in the early detection of dengue virus infection . Any interpretation or use of this test result must also rely on other clinical findings as well as on the professional judgment of healthcare providers.

Recommended For Use:Any person presenting with clinical signs or symptoms consistent with acute dengue infection or dengue fever including: high fever, severe headaches, pain behind the eyes, severe joint and muscle pain, fatigue, nausea, vomiting, and/or skin rash.
Dengue NS1 antigen is released into the blood during viral replication in an infected patient, and is detectable from the first day after the onset of fever up to Day 9. NS1 antigen can be identified before the formation of antibodies, thus making it a beneficial biomarker for early detection of dengue infection, allowing for prompt management of dengue fever.

Snibe Maglumi Rubella lgM is a highly sensitive diagnostic test used for torch detection and monitoring.

Snibe Maglumi Toxo lgM is a highly sensitive diagnostic test used for torch detection and monitoring.

Oscar Elisa test kit-
Dengue- Antigenn- ns1
hIV 3rd gen
HIV 4th Gen
Hepatitis B Elisa test kit
HCV Elisa test kit
Kala Azar Dipstickstest kit
Syphilis Elisa test kit


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Snibe Maglumi Total PSA for 600/800/x3/1000/2000 is a diagnostic test used for detecting and monitoring tumor markers, particularly Prostate Specific Antigen (PSA), on various Maglumi analyzers. These analyzers include models like Maglumi 600, 800, x3, 1000, 2000, and 2000Plus. The test is highly sensitive and can be used to assess PSA levels, which can be elevated in certain conditions, including prostate cancer

BeneSphera™ Prolactin ELISA Kit for the quantitative determination of Prolactin Hormone from human serum and plasma.

• Quantitative determination by sandwich ELISA
• Assay time: 1 h 30 min
• Sensitivity: 0,04 ng which is equivalent to a sample containing 0,8 ng/ml Prolactin concentration
• Specificity: no cross reactivity up to 1000 ng/ml of LH, FSH, TSH, GH and CG

Enzyme Immunoassay for the quantitative determination of Prolactin Hormone concentration in human serum/plasma.

Snibe Maglumi Troponin I is a highly sensitive diagnostic test used for cardiac detection and monitoring.

Snibe Maglumi CMV lgG is a highly sensitive diagnostic test used for torch detection and monitoring.

Vitamin B12 Quanti Microlisa is designed for in-vitro quantitative determination of Vitamin B12 in human serum.

Salient Features

• Principle : Based on competitive immunoassay
• Quantitative detection of Vitamin B12 (cyanocobalamin) in human serum.
• Excellent sensitivity & specificity.
• Linearity Range: 50- 2000 pg/ml.
• Analytical Sensitivity: 50 pg/ml
• Breakaway microwell strips.
• Color coded reagents to monitor procedural steps.
• Assay procedure: 125 mins.
• Prompt service back-up
• Longer shelf life:18 Months at 2-8°C.
• Convenient pack size: 96 tests

BeneSphera™ FT3 ELISA Kit for the quantitative determination of FT3 (Free Triiodothyronine) Hormone from human serum and plasma.

• Assay time: 1 h 30 min
• Expected range: Adult - 1,4 to 4,2 pg/ml, Pregnancy - 1,8 to 4,2 pg/ml
• Sensitivity: 0,05 pg/dl
• Specificity: no interference found, total of 85 samples found to have high degree of correlation with free T3 calibrators provided
• Precision: very low coefficient of variation found in intra-assay and inter-assay reproducibility studies

Enzyme Immunoassay for the quantitative determination of Free T3 Hormone concentration in human serum/plasma.

Malaria Ag Microlisa is an in-vitro qualitative enzyme immunoassay for detecting infection with plasmodium species (P.falciparum /P.vivax/ P.malariae/ P.ovale) based on pLDH antigen in human blood. It is intended for screening of blood donors or other individuals at risk for malaria infection and for clinical diagnostic testing.

Salient Features

• Detection of plasmodium species (P.falciparum /P.vivax/ P.malariae/ P.ovale) based on pLDH antigen in human blood
• Break away wells for minimal wastage
• Easy interpretation of results
• System configuration compatible with all common ELISA equipment
• High analytical Sensitivity of >20 parasites/ul of blood
• Shelf life: 24 Months at 2-8°C
• Color coded reagents to monitor procedural steps
• Assay procedure: 120mins

Dengue IgG Microlisa is designed for in-vitro qualitative detection of Dengue IgG antibodies in human serum or plasma and is used as a screening test for testing of collected blood samples suspected for DENGUE. The kit detects all four subtypes; DEN1, DEN2, DEN3 & DEN4 of Dengue Virus.

Salient Features

• Based on “CAPTURE ELISA” principle
• Detection of all 4 serotypes of Dengue (DEN 1 – DEN 4)
• Colour coded reagents to monitor procedural steps
• Longer Shelf life: 18 months at 2-8°C
• Sensitivity 96.00% & Specificity 99.93%
• Convenient pack size: 96 Tests
• Unique break-away wells
• Prompt service back up

meril dengue Igm:-Enzyme Immunoassay for detection of antibodies (IgG) in human serum or plasma.

RBPL HEV IgM ELISA kit is for qualitative detection of anti-hepatitis E virus IgM in human serum or plasma.

• Utilizes IgM capture technique.

• Suitable for diagnosing acute HEV infection.

• Assay time: 75 Mins.

• Sensitivity: 100% & Specificity: 100%.

• Utilizes IgM capture technique.

• Suitable for diagnosing acute HEV infection.

• Assay time: 75 Mins.

• Sensitivity: 100% & Specificity: 100%.

Dengue NS1 Ag Microlisa is designed for in vitro qualitative detection of Dengue NS1 antigen in human serum or plasma and is used as a screening test for testing of collected blood samples suspected for DENGUE. The kit detects all four subtypes; DEN1, DEN2, DEN3 & DEN4 of Dengue Virus.

Salient Features

• First line testing kit for detecting infection with Dengue NS1 Ag.
• Based on Direct Sandwich Elisa principle
• Detection of all 4 serotypes of Dengue (DEN 1 – DEN 4)
• Color coded reagents to monitor procedural steps
• Significant reduction in window period
• Longer Shelf life: 24 months at 2-8°C.
• Sensitivity 99.50% & Specificity 100%.
• Convenient Packsize: 96 tests

The RecombiLISA Leptospira IgM ELISA Kit is an indirect, solid phase enzyme-linked immunosorbent assay. The two main kit components are:

1) A 96 breakable well plate with the solid microwells pre-coated with L. interrogans antigen.

2) Liquid conjugates composed of monoclonal anti-human IgM reagent conjugated with horseradish peroxidase (HRP-anti-human IgM conjugates).

This test is intended to be used for the qualitative detection of IgM anti-Leptospira interrogans (L. interrogans) in human serum or plasma. It is intended to be used by professionals as an aid in the diagnosis of acute infection with L. interrogans. Any interpretation or use of this test result must also rely on other clinical findings as well as on the professional judgment of health care providers.

Recommended For Use:

• Any person presenting with clinical signs or symptoms consistent with acute infection with interrogansincluding: high fever, headache, chills, muscle aches, vomiting, jaundice, red eyes, abdominal pain, diarrhea, skin rash

• After exposure to a known contaminated source

BeneSphera™ FT4 ELISA Kit for the quantitative determination of FT4 (Free thyroxine) Hormone from human serum and plasma.

• Expected range: Adult - 0,8 to 2,0 ng/dl, Pregnancy - 0,76 to 2,24 ng/dl
• Sensitivity: 0,05 ng/dl
• Specificity: no interference found, total of 197 samples found to have high degree of correlation with free T4 calibrators provided
• Precision: very low coefficient of variation found in intra-assay and inter-assay reproducibility studies

Enzyme Immunoassay for the quantitative determination of Free T4 Hormone concentration in human serum/plasma.

BeneSphera™ FSH ELISA Kit for the quantitative determination of FSH (Follicle-stimulating hormone) Hormone from human serum and plasma.

• Quantitative determination by sandwich ELISA
• Assay time: 1 h 30 min
• Sensitivity: 0,02 mIU/ml which is equivalent to a sample containing 0,8 mIU/ml FSH concentration
• Specificity: no cross reactivity

Enzyme Immunoassay for the quantitative determination of FSH Hormone concentration in human serum/plasma.