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Brucella Set

$1.00
A Brucella Set is a comprehensive serological test system (Class II medical device, CE-marked/FDA-cleared) for qualitative and quantitative detection of antibodies against Brucella species (B. abortus, B. melitensis, B. suis, B. canis) using multiple methodologies including tube agglutination, slide agglutination, and 2-mercaptoethanol (2-ME) testing. The set includes killed, stained Brucella antigens, positive and negative controls, dilution tubes, reaction cards, and 2-ME reagent for IgM/IgG differentiation. Diagnostic titer ≥1:160 or fourfold rise confirms brucellosis. Primary clinical applications include diagnosis of brucellosis in endemic regions (undulant fever, night sweats, arthralgia), fever of unknown origin investigation, occupational health screening in high-risk workers (veterinarians, farmers, slaughterhouse workers), diagnosis of focal complications (sacroiliitis, spondylitis, meningitis, endocarditis), treatment monitoring (fourfold decline indicates response), outbreak investigation, and public health surveillance. Critical safety precautions include handling all samples in biosafety cabinet (Brucella is highly infectious via aerosol), 2-ME reagent toxicity (use fume hood), awareness of prozone phenomenon (serial dilutions essential), cross-reactions with other Gram-negative bacteria, and mandatory reporting to public health authorities. Essential test for brucellosis diagnosis in endemic regions and occupational health settings.

Rheumatoid factor

$1.00
Rheumatoid Factor (RF) testing is a quantitative or semi-quantitative serological assay (nephelometry, turbidimetry, latex agglutination, or ELISA) for detecting autoantibodies against the Fc portion of immunoglobulin G, primarily of the IgM isotype. RF is a key marker in the ACR/EULAR classification criteria for rheumatoid arthritis, with sensitivity 60-80% and specificity 70-90%. Test requires serum samples; results reported in IU/mL (reference <15-20 IU/mL) or titer. Primary clinical applications include diagnosis and classification of rheumatoid arthritis, prognostic assessment (high-titer RF correlates with severe, erosive disease), differential diagnosis of inflammatory arthritis, monitoring disease activity, diagnosis of Sjögren's syndrome, evaluation of mixed cryoglobulinemia (hepatitis C-associated), and assessment of other autoimmune and chronic inflammatory conditions. Critical safety precautions include awareness of false positives (other autoimmune diseases, chronic infections, healthy elderly), false negatives (seronegative RA 20-30%), need for clinical correlation, and anti-CCP antibody testing to improve diagnostic accuracy. Essential test for rheumatology practice, autoimmune disease evaluation, and differential diagnosis of inflammatory arthritis.