SYPHILIS

SYPHILIS

Intro

The serological diagnosis of syphilis is performed by demonstrating the presence of significant levels of specific Treponema pallidum (TP) antibodies in the serum sample. The reference method used is the FTA-ABS
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Products

SYPHILIS SCREEN RECOMBINANT

coated with recombinant proteins of Treponema pallidum antigens

Kit for the determination of anti-Treponema pallidum (Nichols strain) immunoglobulins in human serum, using recombinant antigens. Immunoenzymatic method.

Data sheet

Code
91100
Quantity
2X96 tests
METHOD
Indirect ELISA
TYPE
Qualitative Test
DIAGNOSTIC SENSITIVITY
100%
DIAGNOSTIC SPECIFITY
99.9%
INCUBATION TIME
50 min
SHELF LIFE
15 months from the date of preparation
STORAGE and STABILITY
2°/8°C

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TREPONEMA IgG

coated with a pool of recombinant proteins of Treponema pallidum

Kit for the determination of anti-Treponema pallidum (Nichols strain) IgG antibodies in human serum. Recombinant antigen.

Data sheet

Code
91050
Quantity
96 tests
METHOD
Indirect ELISA
TYPE
Qualitative Test
DIAGNOSTIC SENSITIVITY
97.4%
DIAGNOSTIC SPECIFITY
100% CI95%: 97.1. – 100
INCUBATION TIME
105 min
SHELF LIFE
15 months from the date of preparation
STORAGE and STABILITY
2°/8°C

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TREPONEMA IgM

coated with anti-human IgM monoclonal antibodies

Kit for the determination of anti-Treponema pallidum (Nichols strain) IgM antibodies in human serum. Recombinant antigen. Capture method.

Data sheet

Code
91051
Quantity
96 tests
METHOD
CAPTURE ASSAY
TYPE
Qualitative Test
DIAGNOSTIC SENSITIVITY
92%
DIAGNOSTIC SPECIFITY
100% CI95%: 97.1. – 100
INCUBATION TIME
105 min
SHELF LIFE
15 months from the date of preparation
STORAGE and STABILITY
2°/8°C

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