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Cambridge Life Sciences - Immunology - Vasculitis - Anti-Glomerular Basement Membrane (GBM) antibodies
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Immunology Clinical Chemistry Urease Hp Tests Instrumentation

Vasculitis

Anti-Glomerular Basement Membrane (GBM) antibodies

Glomerular nephritis is a major cause of irreversible renal failure. Many forms of glomerular nephritis are caused by immunological mechanisms associated with autoimmunity. One particular type of glomerular nephritis is caused by Goodpasture’s Syndrome (GS).

GS is an autoantibody mediated glomerular nephritis characterised by the presence of antibodies to the a 3 chain of type IV collagen which is the specific antigenic determinant for the glomerular basement membrane (GBM). Diagnosis is based on a combination of clinical features and laboratory tests. The presence of kidney lesions (crescent formation in the glomeruli) gives an indication of kidney damage but is not considered specific.

Indirect immunofluorescence (IFA) using monkey kidney sections for the detection of antibodies to GBM is useful but is regarded as less sensitive and less specific than BlueDot and is often difficult to interpret.

 

The various product formats are listed below:

Code
Name
Description
Determinations
1124 ImmuGlo Anti-GBM Kit 8 x 6 well Monkey Kidney slides

48

2100 ImmuGlo IgG FITC Conjugate anti-human IgG for indirect IF

5.0mL

2163 ImmuGlo Anti-GBM Slide Primate kidney substrate slide

6 well

2200 ImmuGlo Negative Control  

0.5mL

2267 ImmuGlo Anti-GBM Positive Control  

0.5mL

For technical information on Immco products please click here or contact us.

D-tek BlueDot - Immunodot
Code
Name
Description
Determinations

ANCAGD-24

BlueDot ANCA+GBM IgG MPO, PR3, GBM

24

GBD-24 BlueDot GBM IgG GBM

24

For technical information on D-tek products please click here or contact us.

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Immunology     Clinical Chemistry    Urease Hp Tests     Instrumentation