Home·NEXTGEN IN-VITRO DIAGNOSTICS PRIVATE LIMITED·Products·EnBind™ ELISA Kits

EnBind™ ELISA Kits

Certificates:ISO 9001:2015ISO 13485:2016ISO 14001:2015cGMP
NEXTGEN IN-VITRO DIAGNOSTICS PRIVATE LIMITEDSouth Delhi, DL
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Anchored to the MCA registerCIN U33110DL2015PTC279481
Price on request. Ask the factory for a quote.
MOQ not stated Lead time on requestCurrency INR
Customization for this product
  • OEM (your brand on our product)
Key attributesAll specs
Category
ELISA Kits
Place of origin
South Delhi, DL, India

Highlights at a glance

  • Category: ELISA Kits
  • Made in South Delhi, DL, India
  • Certified: ISO 9001:2015, ISO 13485:2016, ISO 14001:2015

Description

ELISA (Enzyme-Linked Immunosorbent Assay) is a highly sensitive and specific immunoassay platform for the quantitative determination of a wide range of analytes. Our ELISA kits utilise precise antibody-antigen interactions to deliver reliable and reproducible results.

General Specifications

Product Type: Enzyme-Linked Immunosorbent Assay (ELISA) Kits Intended Use: For qualitative and/or quantitative detection of specific antigens, antibodies, or biomarkers in human serum, plasma, or other biological fluids. Suitable for clinical diagnostics and research applications

General Characteristics

Format: 96-well microplate (12 × 8 strips, breakable) Assay Principle: Sandwich/indirect/competitive ELISA (parameter dependent) Detection System: Horseradish peroxidase (HRP) with TMB chromogenic substrate Specimen Type: Human serum, plasma or urine (depending on parameter) Sample Volume: Typically 50–100 µl per well Assay Time: 60–120 minutes (protocol dependent) Readout: Optical density measurement at 450 nm (reference 620–630 nm) Storage Condition: 2–8°C (do not freeze) Shelf Life: 12–18 months from date of manufacture Kit Size: 96 tests per kit (other formats available on request)

Performance Characteristics

Sensitivity: Optimised for low-level detection of analyte (parameter specific) Specificity: High specificity through proprietary antibodies/antigens, minimal cross-reactivity Precision: CV ≤10% intra- and inter-assay variation Dynamic Range: Wide linear range suitable for clinical decision-making Accuracy: Validated against gold-standard reference methods

Trade & shipping terms

Set by NEXTGEN IN-VITRO DIAGNOSTICS PRIVATE LIMITED — the supplier's own terms.

CustomisationOEM Available

Certificates

ISO 9001:2015
ISO 13485:2016
ISO 14001:2015
cGMP

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NEXTGEN IN-VITRO DIAGNOSTICS PRIVATE LIMITED
Unverified<1 yr on BharatSealSouth Delhi, Delhi
Year founded
2015
Certifications
4

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