Thuis Producten Voorzieningen voor medische tests

Chikungunya Virus Rapid Test Cassette Colloidal Gold for IgM/IgG Antibody Detection

Name: Chikungunya Virus Rapid Test Cassette Colloidal Gold for IgM/IgG Antibody Detection
Brand: Sichuan Hundred Medcal Technology Co., Ltd.
SKU: /
Availability: InStock

Alle producten

Huishoudelijk medisch apparaat
(42)

Medische beschermingsbenodigdheden
(13)

Medisch tandheelkundig apparaat
(23)

Chirurgisch verbruiksgoed
(35)

Medische analysator
(12)

Voorzieningen voor medische tests
(21)

medische diagnostische apparatuur
(41)

Noodreddingsapparatuur
(13)

apparatuur voor ademhalingstherapie
(5)

medische bewakingsapparatuur
(10)

Medische producten voor de gezondheidszorg
(25)

Gekronkelde Zorglevering
(6)

Medische sterilisatieapparatuur
(1)

Revalidatie Medische Apparatuur
(14)

Hyperbare apparatuur
(2)

Certificaat

China Sichuan Hundred Medcal Technology Co., Ltd. certificaten

Ik ben online Chatten Nu

Chikungunya Virus Rapid Test Cassette Colloidal Gold for IgM/IgG Antibody Detection

Grote Afbeelding : Chikungunya Virus Rapid Test Cassette Colloidal Gold for IgM/IgG Antibody Detection

Productdetails:

Plaats van herkomst:	China
Merknaam:	HDRMEDICO
Certificering:	CE
Modelnummer:	/

Betalen & Verzenden Algemene voorwaarden:

Min. bestelaantal:	500 stuks
Prijs:	Bespreekbaar
Verpakking Details:	Karton
Levertijd:	10-15 dagen
Betalingscondities:	L/C, T/T, Westen Union, Money Gram, PayPal/VTB
Levering vermogen:	100000PC/maand

Contact Praatje Nu

Chikungunya Virus Rapid Test Cassette Colloidal Gold for IgM/IgG Antibody Detection

beschrijving

Productnaam:	Chikungunya-virus sneltestcassette	Materiaal:	Plastic
Productcategorie:	In vitro-diagnose	Methode:	Colloïdale goudmethode
Houdbaarheid:	Twee jaar	Functie:	Detectie
Markeren:	Chikungunya virus rapid test cassette , Colloidal gold antibody detection test , IgM IgG rapid test cassette

Chikungunya Virus Rapid Test Cassette

This in vitro diagnostic device utilizes immunochromatographic (colloidal gold) technology for the rapid, qualitative detection of anti-Chikungunya virus IgM and IgG antibodies in human serum, plasma, or whole blood samples.

Technology & Methodology

The test operates on a lateral flow immunoassay principle. Recombinant Chikungunya virus antigens are immobilized on the nitrocellulose membrane at distinct test lines (T-IgM and T-IgG). When a sample is applied, anti-CHIKV antibodies bind to the antigen-colloidal gold conjugate, forming visible colored lines at the respective test lines.

Intended Use & Clinical Applications

This rapid test serves as an important aid in the presumptive diagnosis of recent or past Chikungunya virus infection, particularly useful in:

Outbreak Settings: Rapid screening of febrile patients in areas with active CHIKV transmission
Differential Diagnosis: Distinguishing Chikungunya fever from other clinically similar arboviral diseases such as dengue or Zika virus infection
Case Management: Supporting clinical decision-making for patients with acute onset of high fever and severe joint pain

Key Features & Advantages

Rapid Results: Visual results typically within 10-20 minutes for quick clinical triage
Simultaneous Detection: Detects both IgM (recent infection) and IgG (later stage or past infection) antibodies from a single sample
Ease of Use: Simple procedure requiring minimal training and no specialized laboratory equipment
High Clinical Utility: Positive IgM result with compatible symptoms strongly suggests acute Chikungunya infection

Result Interpretation

Result	Interpretation
IgM Positive	Suggests recent or current Chikungunya virus infection
IgG Positive	Indicates later-stage or past infection/exposure
Both IgM & IgG Positive	Common during the convalescent phase
Negative	No detectable levels of anti-CHIKV antibodies (does not completely rule out early infection)
Invalid	Control line (C) fails to appear - test must be repeated

Important Notes

This is a screening test. All reactive results, especially in low-prevalence areas, should be confirmed by more specific serological methods (ELISA, PRNT) or molecular tests (RT-PCR) in a reference laboratory. Test performance may vary depending on sample collection timing relative to symptom onset. Clinical history and epidemiological context are essential for accurate diagnosis.

label:

Contactpersoon: Mr. Terry

Tel.: 15008220675

Andere Producten