Serum and Urine Immunofixation

Identification of monoclonal proteins by agarose gel electrophoresis.

About Serum and Urine Immunofixation

Immunofixation is an immunological method for detection and identification of monoclonal proteins in serum and urine. After the separation of serum and urine proteins according to their charge, the gel is incubated with different specific antisera. The gel is then processed in order to remove the antisera and unbound protein prior to the final staining step. The gel is interpreted visually to type all immunoglobulins.

Sebia HYDRAGEL BENCE JONES Gel, provided by the HYDRASYS 2 SCAN FOCUSING instrument

Pathologies associées

Multiple Myeloma

Technologies utilisées

Gel Electrophoresis

Key benefits

High quality serum and urine immunofixation for accurate monoclonal component identification.

Good performance
for proteins separation and identification of monoclonal component in serum and urine in agarose gel method.
Clear band visualization
in serum and urine for quick identification of suspect monoclonal proteins IgG, IgA, IgM, Kappa (κ) or Lambda (λ) and free light chains involved in gammopathy.
High quality, ready to use antisera
for optimal reaction performance and accurate monoclonal component identification.
Complete semi-automated
HYDRASYS 2 SCAN FOCUSING system performing sample application, electrophoretic migration, staining, destaining and scanning when connected to PHORESIS Software for interpretation, data & result management.
Dedicated HYDRAGEL BENCE JONES kits
for detection of very small monoclonal components.

Main characteristics

Test principle

The HYDRAGEL IF assay is based on the principle of agarose gel electrophoresis followed by immunofixation.
After the separation of serum or urine proteins according to their charge, the gel is incubated with different specific antisera for characterization of monoclonal component involved in the gammopathy.

Sample type

Serum & Urine

Performances

Sensitivity

The minimal detection limit for monoclonal immunoglobulins is about 120 mg/L for gels stained with acid violet.
According to the mobility of the monoclonal component and polyclonal background, the sensitivity may vary.

Internal sensitivity study demonstrated that a Bence Jones protein can be detected in a serum at a concentration:

as low as 20 mg/L with anti-free & bound light chains antisera
as low as 50 mg/L with anti-free light chains antisera

Product details

HYDRAGEL 1 IF (SM*) – P/N: 4801 / (DM**) – P/N: 4301
HYDRAGEL 2 IF (SM) – P/N: 4802 / (DM) – P/N: 4302
HYDRAGEL 4 IF (SM) – P/N: 4804 / (DM) – P/N: 4304
HYDRAGEL 9 IF (SM) – P/N: 4809 / (DM) – P/N: 4309
HYDRAGEL 1 BENCE JONES (SM) – P/N: 4821 / (DM) – P/N: 4321
HYDRAGEL 2 BENCE JONES (SM) – P/N: 4822 / (DM) – P/N: 4322
HYDRAGEL 4 BENCE JONES (SM) – P/N: 4824 / (DM) – P/N: 4324
HYDRAGEL 2 URINE PROFIL(E) (SM) – P/N: 4831 / (DM) – P/N: 4331
HYDRAGEL 4 URINE PROFIL(E) (SM) – P/N: 4832 / (DM) – P/N: 4332

*SM: Standard Mask

** DM: Dynamic Mask

Knowledge & Science

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