DRX Laboratories India Inc

Bioline™ HCV test is a immunochromatographic rapid test for the qualitative detection of antibodies specific to HCV in human serum, plasma or whole blood. Recombinant HCV core, NS3, NS4, NS5 Ag used as capture materials

We, DRx Laboratories India Inc., have quickly become one of the leading traders and suppliers, focusing on providing innovative solutions to the health care and research industries. We concentrate on providing superior-quality products, including Biochemistry Analyzers, Clinical Chemistry Analyzers, Coagulation Analyzers, Hematology Analyzers, Microplate Readers, Eiawash Plate, etc.

Hepalisa is designed for in – vitro qualitative detection of Hepatitis B Surface antigen (HBsAg) in human serum or plasma and is used as a screening test for testing of collected blood prior to transfusion.

Salient Features

• Detects all the known 11-subtypes of HBV
• Antigen Sensitivity-0.1ng/ml.
• Two step Immunoassay.
• Short protocol: Based on single washing step.
• Assay Procedure: 90 mins.
• Shelf life-24 months at 2-8°C.
• Convenient pack size :96 tests
• Break-away wells for minimal wastage
• Easy interpretation of result
• Sensitivity & Specificity 100% by WHO.

Principle

Hepalisa is a solid phase enzyme linked immunosorbent assay based on the Direct Sandwich Elisa principle. The microwells are coated with Monoclonal antibodies with high reactivity for HBsAg. The samples are added in the wells followed by addition of enzyme conjugate (polyclonal antibodies linked to Horseradish Peroxidase (HRPO). A sandwich complex is formed in the well wherein HBsAg (from serum sample) is “trapped” or “sandwiched” between the antibody and antibody HRPO conjugate. Unbound conjugate is then washed off with wash buffer.

The 3rd generation HCV Microlisa is an in vitro qualitative enzyme linked immunosorbent assay for the detection of antibodies against HCV (anti-HCVs) in human serum or plasma. The kit is basically intended to screen blood donations to identify and eliminate the infected units of blood and for clinical diagnostic testing.

Salient Features

• 3rd Generation Assay
• Unique combination of HCV antigens for E1, E2, Core, NS3, NS4 & NS5
• Break-away microwell strips
• Based on Indirect Elisa principle
• Colour coded reagents to monitor procedural steps.
• Short assay procedure: 90mins
• Longer shelf life: 24 months at 2-8°C.
• Sensitivity 100% & Specificity 97.4% by WHO.

Principle

The 3rd generation HCV Microlisa is based on a highly sensitive technique, Enzyme linked Immunosorbent Assay which detects antibodies against HCV in human serum and plasma. The HCV proteins are present in serum at levels well below the limits of detection. Thus immunodiagnosis of HCV infection is based on detection of host generated antibodies (anti-HCVs) to viral proteins. The 3rd generation HCV Microlisa utilizes a combination of antigen with the sequence of both HCV structural and non-structural antigens i.e. CORE, E1, E2, NS3, NS4 and NS5. It has an obvious advantage over the available 2nd Generation and 1st Generation Elisa with improved sensitivity and specificity. The combination of antigens for the structural and non-structural HCV proteins is coated onto the microwells. Diluted sample and controls are then incubated. Antibodies to HCV, if present, bind to the immobilized HCV antigens on the microwell during this incubation period.

Description:

• Onsite Rapid Test
• A-10 Minutes Lateral flow immunoassay for the qualitative detection of hemoglobin in human fecal specimen at detection senstivity of 25 ng/ml

Contains

• 25 Individually packed cassette
• 25 Stool Collection Devices
• 25 Patient ID Stickers
• 1 Package insert
• FOB-Hi Rapid Test
• A-10 Minute Lateral Flow Immunoasssay For The Quantitative Detection Of Hemoglobin in human Fecal Specimenat Detection Sebsyivity Of 25 ng/ml
• REF-R2011C
• LOT-FQ22153E00D

Description:

• TRI-DOT
• Rapid Visual Test for The Detection Of Antibodies To Hepatine Gavirus in Human Serum Plasma
• HCV Antigens for Core, NS3, NS4, & NS5

4TH Generation Microlisa HIV Ag & Ab is an in- vitro qualitative enzyme immunoassay for the detection of antibodies to HIV-1 and/or HIV-2 and HIV-1 p24 antigen in human serum or plasma. It is intended for screening of blood donors or other individuals at risk for HIV-1 and/or HIV-2 infection and for clinical diagnostic testing.

Salient Features

• Use of Envelope Antigens gp41, C terminus of gp120 for HIV-1 and gp36 for HIV-2 & simultaneously detection of p24 antigen with p24 monoclonal antibodies
• Detection of Group O & subtype C for HIV-1 prevalent in India
• Colour coded reagents to monitor the procedural steps
• Assay procedure: 120 mins
• Shelf life: 18 months at 2-8°C
• Sensitivity 100% & Specificity 99.97%
• Significant reduction in window period
• Easy to use on automated and semi-automatic processor

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

Fast Results

Within 1 hr 10 min.

Easy to Use

Standardised Indirect ELISA procedure.

Time Efficient IgM

No need to incubate RF absorbent and serum prior to addition to antigen-coated wells.

Cost Effective

Incorporates break apart wells.

High Sensitivity

Detects IgM antibodies to a broad range of serovars.

We are DRx Laboratories India Inc  based at New Delhi , we are supplier and exporter medical goods and we have special price for mission , Abbott , Meril , Jmitra , SNIBE , ARKRAY 

Established in 2021, DRx Laboratories India Inc has made a well-recognized name as a Wholesaler and Trader of Rapid Test Kit, HIV Test Kit and More.

Established in 2021, DRx Laboratories India Inc has made a well-recognized name as a Wholesaler and Trader of Rapid Test Kit, HIV Test Kit and More.

Established in 2021, DRx Laboratories India Inc has made a well-recognized name as a Wholesaler and Trader of Rapid Test Kit, HIV Test Kit and More.

Established in 2021, DRx Laboratories India Inc has made a well-recognized name as a Wholesaler and Trader of Rapid Test Kit, HIV Test Kit and More.

Description

• For In Vitro Diagnostic use Only
• Store At 2- 30 Degree Celsius Sealed
• REF : RQ213C
• IVD
• Lot No: F0207S4A01
• Mfg Date: 2021-02-08
• Exp Date: 2023-02-07
• HSV-2 IgG/IgM Rapid Test
• Not to be sold loose
• Confirm Reactive Results with Confirmatives Tests Like Virus Culture/Elisa/PCR, etc

Description:

• HBsAg Rapid Test device Serum/Plasma
• IVD
• Lateral flow Immunochromatographic test
• Max Line HBsAg Rapid Test Device Serum/Plasma
• Store At 4-30 Degree celsius

Description

• Tsutsugamushi IgM/IgG
• One step rapid immunochromatographic Assayfor qualitative detection of IgM/IgG antibodies to Orientia tsutsugamushi in human serum plasma or whole blood
• QC pass

Contents

• Standard Q* Tsutsugamushi IgM/IgG Cassette x 20
• Specimen transfer device 10microl x 20
• Buffer bottle 4ml x 01
• Instruction for use x 01
• Lot No: C029016
• Mfg Date: 08/2021
• Exp Date: 07/2023
• SD/029/1B/01-00

Description

• One Step test For HBsAg
• For in vitro diagnostics use only
• Meriscreen HBsAg

Bioline™ Rotavirus test is an immunochromatographic assay for the detection of Group A rotavirus in fecal specimens. The test utilizes two kinds of antibody in a solid phase sandwich immunochromatography to detect group specific proteins, including the major inner capsid protein, present in Group A rotaviruses.

We, DRx Laboratories India Inc., have quickly become one of the leading traders and suppliers, focusing on providing innovative solutions to the health care and research industries. We concentrate on providing superior-quality products, including Biochemistry Analyzers, Clinical Chemistry Analyzers, Coagulation Analyzers, Hematology Analyzers, Microplate Readers, Eiawash Plate, etc.

Description:

• One Step Rapid Immunochromatographic
• test for the qualitative detectionof hepatitis B Surface antigen (HBsAg)
• From Serum Or Plasma
• 50 micro litre specimen
• HSV-2IgG/IgM Rapid Test
• Pack Size:10 Tests/Kit
• Lot no:F0207S4A01
• Mfg.Dt:2021-02-08
• Exp.Dt:2023-02-07
• Import License no.IMP/IVD/2019/000307
• Confirm Reactive Results with Confirmative Tests Like Virus culture ?ELISA/PCR,etc.)
• Not To Be Sold loose
• PL-R0213C-3-10T-ATH-Rav AP1