Endotoxin Lal Test Kit

Endotoxin Lal Test Kit Specification

Material
Reagent grade, sterile

Color Code
White/Blue

Properties
High sensitivity, rapid results, compliance with pharmacopoeia standards

Dimension (L*W*H)
Box: 10 x 5 x 5 cm

Function
Endotoxin testing

Weight
Approx. 200 g

Application
Detection of endotoxins in pharmaceuticals, medical devices, water, biological products

Shape
Rectangular kit box

Temperature Range
28C (storage)

Phase
Single Phase

Height
5 cm (box height)

Treatment Type
Diagnostic

Storage Capacity
Sufficient for 25 tests

Accuracy
Detection as low as 0.01 EU/ml

Humidity Range
Store at 28C, avoid moisture

Suitable For
Laboratory, pharmaceutical, medical device industry

Use
Quantitative and qualitative detection of endotoxin

Product Type
Endotoxin LAL Test Kit

Automation Grade
Manual

Reactivity
Detects gram-negative bacterial endotoxins

Regulatory Compliance
USP, EP, JP Pharmacopoeia compliant

Sample Requirements
Pyrogen-free containers

Packaging Type
Boxed Kit

Included Components
LAL reagent vials, Control vials, Endotoxin-free accessories, Instructions

Shelf Life
Typically 12-24 months from manufacturing

Test Method
Gel Clot/LAL-based Assay

Time to Result
~30-60 minutes per assay

Sensitivity
Down to 0.01 EU/ml (varies by kit type)

Endotoxin Lal Test Kit Trade Information

FOB Port
mumbai

Payment Terms
Cash Against Delivery (CAD), Cash Advance (CA), Cash in Advance (CID), Cheque

Delivery Time
1 Week

Sample Available
Yes

Sample Policy
Free samples are available

Main Export Market(s)
Middle East, Africa, Asia

Main Domestic Market
All India

About Endotoxin Lal Test Kit

Assisted by a hardworking team and modern trading set up, our firm is engaged in offering the Limulus Amebocyte Lysate Kit (Lal). This kit finds in the outer cell membrane of gram-negative bacteria. It can impact over 30 biological activities. Our offered kit is an economical choice for water samples and large volume parenterals. In addition, this Limulus Amebocyte Lysate Kit (Lal) provides the benefit of product interference for proteins, vaccines and other biologicals.

Features:

It is a sustainable endotoxin detection method
It is not derived from horseshoe crab blood
Provides a simple positive & negative results

Technical Specifications

Other Name	Bacterial Endotoxin Lal Test Kit
Shelf Life	24 to 36 months
Sample Type	bet
Sensitivity	0.125/0.03/0.06
Packaging Type	100 test
Packaging Size	5 vials

Rapid, Sensitive Endotoxin Detection

This test kit employs a highly sensitive LAL-based gel clot assay method, capable of detecting endotoxin concentrations as low as 0.01 EU/ml. Results are rapidly obtained within 30 to 60 minutes, making it ideal for both routine quality control and urgent diagnostic needs in pharmaceutical or medical device applications.

Pharmacopoeia Compliance for High Reliability

Fully compliant with major pharmacopoeia standards (USP, EP, JP), the kit ensures consistent, regulatory-approved performance. Its inclusion of validated reagents and controls supports reliable and reproducible data, satisfying stringent industry requirements for endotoxin testing.

Comprehensive Kit for Easy Use

Every kit arrives neatly boxed and provides all essentials for 25 tests, including LAL reagents, control vials, endotoxin-free tools, and clear instructions. Its compact design (10 x 5 x 5 cm) ensures it fits efficiently in various laboratory setups while maintaining sterility and convenience.

FAQs of Endotoxin Lal Test Kit:

Q: How does the Endotoxin LAL Test Kit detect endotoxins in samples?

A: The kit utilizes a gel clot/LAL-based assay, which reacts specifically to gram-negative bacterial endotoxins in the sample. When endotoxins are present, the LAL reagent forms a gel clot, indicating a positive result. This allows both qualitative and quantitative detection.

Q: What is the process for using the kit, and how long does testing take?

A: To use the kit, samples must be collected in pyrogen-free containers and mixed with the included reagents according to the instructions. The assay then runs for approximately 3060 minutes, after which results can be interpreted visually or quantitatively, depending on the procedure followed.

Q: When and where should the kit be stored to maintain its effectiveness?

A: The kit must be stored at 28C in a dry environment to preserve the activity and sterility of its reagent grade materials. Avoid exposing the kit to moisture to prevent contamination and degradation of reagents.

Q: What are the main benefits of using this LAL Test Kit?

A: Key benefits include high sensitivity (detects as low as 0.01 EU/ml), rapid results within an hour, box-packaged convenience, and compliance with leading pharmacopoeia standards. This makes it ideal for reliable quality assurance in production or laboratory environments.

Q: Which types of samples and industries can utilize this kit?

A: The kit is suitable for testing water, pharmaceuticals, medical devices, intermediate bulks, and biological products in laboratory settings, pharmaceutical manufacturing, and the medical device industry. Samples must always be collected in pyrogen-free containers.

Q: How accurate and reliable are the results provided by the kit?

A: The test delivers accurate detection down to 0.01 EU/ml, ensuring trustworthy results for low-level endotoxin contamination. Inclusion of control vials and compliance with USP, EP, and JP standards further guarantees consistency and reliability.

Q: What components are included in the kit, and how many tests can it perform?

A: Each kit contains LAL reagent vials, control vials, endotoxin-free accessories, and detailed instructions in a sterile boxed format. It provides sufficient materials to perform up to 25 endotoxin tests.