Typhoid IgG/IgM Test
Typhoid IgG/IgM Test

Typhoid IgG/IgM Test

The SAFECARE Typhoid IgG/IgM Rapid Test Device is a chromatographic immunoassay designed for the qualitative detection of IgG and IgM antibodies against Salmonella typhi in whole blood, serum, or plasma specimens. Its core function is to assist healthcare professionals and point-of-care (POC) professionals in the diagnosis of Salmonella typhi infection by identifying specific antibodies in clinical samples.
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Product Overview

The SAFECARE Typhoid IgG/IgM Rapid Test Device is a chromatographic immunoassay designed for the qualitative detection of IgG and IgM antibodies against Salmonella typhi in whole blood, serum, or plasma specimens. Its core function is to assist healthcare professionals and point-of-care (POC) professionals in the diagnosis of Salmonella typhi infection by identifying specific antibodies in clinical samples.

Disease Background

The test targets infections caused by Salmonella typhi, a pathogenic bacterium primarily responsible for typhoid fever. Typhoid fever is a contagious bacterial infection that typically spreads through contaminated food or water. It can lead to severe systemic symptoms (e.g., persistent high fever, abdominal pain, fatigue, and gastrointestinal disturbances) if not diagnosed and treated promptly.


The detection of Salmonella typhi-specific antibodies (IgM and IgG) is critical for clinical diagnosis:IgM antibodies usually appear in the early stage of infection, indicating a fresh/acute infection; IgG antibodies emerge later and may persist for a longer period, suggesting a recent or recurrent infection.
This test aids in distinguishing the stage of infection by detecting both antibody types, supporting timely clinical intervention.

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Ordering Information

 

 

Product Name

Catalog No.

Specimen

Format

Certification

Typhoid IgG/IgM Test

TYP-3022

Serum/Plasma

Cassette

CE

TYP-4022

Whole Blood/Serum/Plasma

Cassette

CE

 

Product Advantages

 

 

 

1

Broad Specimen Compatibility: Works with three common specimen types (whole blood, serum, plasma), eliminating restrictions on sample collection and enhancing usability in diverse clinical settings (e.g., POC clinics, hospitals).

2

Rapid Result Turnaround: Delivers interpretable results within 15 minutes (no interpretation after 20 minutes), enabling quick clinical decision-making and reducing patient waiting time.

3

High Diagnostic Accuracy: Clinically validated against commercial typhoid rapid tests, with a sensitivity of 98.7% and a specificity of 98.7%-ensures reliable detection of Salmonella typhi antibodies and minimizes false-positive/negative rates.

4

Convenient Storage & Stability: Can be stored at room temperature (4-30℃/39-86℉) in its sealed pouch, with stability guaranteed until the expiration date printed on the label. No special cold-chain storage is required, reducing logistics and storage costs.

5

User-Friendly Design: Comes with all necessary materials (test device, instruction manual, dropper, buffer, desiccant) and clear operation steps, suitable for use by healthcare professionals at POC sites without complex training.

 

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Operation Steps

 

 

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FAQ

 

 

Q: What if the sample volume is insufficient?

A: Insufficient sample may cause invalid results (no C line). Repeat with 35μL sample.

Q: Can weak test lines be considered positive?

A: Yes, weak lines indicate low antibody levels but still confirm positivity.

Q: How to handle invalid tests?

A: Ensure proper sample application and repeat with a new kit. Contact distributor if issues persist.

Q: Storage requirements?

A: Store at 2–8°C (36–46°F) for serum/plasma (≤7 days) or -20°C (-4°F) for long-term storage. Use whole blood immediately.

Q: Is the test reusable?

A: No. Single-use only.

 

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