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Diphtheria toxin 5S IgG plus ELISA

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Catalog no.30113622
Regulatory Status
EU: CE
Kit size
12 x 8
Method
ELISA
Incubation time
1 x 1 h, 1 x 30 min, 1 x 15 min
Standard range
0 - 1.000 IU/ml
Specimen / Volumes
10 µL serum, plasma
Substrate / isotope
TMB 450 nm
instructions for usecertificateMSDS

Enzyme immunoassay for the quantitative determination of IgG class antibodies against Corynebacterium diphtheriae toxin in human serum or plasma (citrate). Corynebacteria are aerobic non spore-forming gram-positive rods of irregular shape (0.5 –1 μm thick and 2- 6 μm long). They comprise skin commensals, opportunist pathogens and several major pathogens, including Corynebacterium diphtheriae. In general, they are isolated from throat swabs on selective media containing tellurite. The bacterial infection caused by C. diphtheriae, Diphtheria, has two forms. Respiratory diphtheria is typically caused by toxin-producing (toxigenic) strains; cutaneous disease can be caused by either toxigenic or nontoxigenic strains. In the respiratory form of the disease, a membrane is formed; this membrane is usually visible on the throat or tonsils. Persons may die from asphyxiation when the membrane obstructs breathing. Other complications are caused by remote effects of the diphtheria toxin (myocarditis, nerve paralysis) Cutaneous diphtheria is usually mild, typically consisting of non-distinctive sores or shallow ulcers and only rarely involving toxic complications (1-2% of infections with toxigenic strains). Diphtheria was one of the most common causes of death among children during the prevaccine era. Since the introduction and widespread use of diphtheria toxoid vaccine (formalin-inactivated diphtheria toxin) in most industrialized countries the disease is now characterized by sporadic cases and intermittent outbreaks of low intensity. But recent large epidemics of diphtheria in several eastern European countries have again drawn attention to this „forgotten“ disease – and, the majority of these cases have occurred among adolescents and adults instead of children.

For concrete data please consult the Instruction for Use in the download box on the top right side.

Our Product Families

Our comprehensive immunoassay portfolio includes a number of specialty diagnostic immunoassays for endocrinology, immunology and autoimmunity, as well as for diagnosis of multiple infectious diseases. We are pioneers and market leaders in saliva diagnostics, with over 40 years of experience supplying a broad portfolio of luminescence- and ELISA-based tests, including our highly acclaimed HMGB1 and MuSK-Ab ELISAs.

And as experts in laboratory automation, we can support our customers with the protocols for open ELISA platforms, such as the Freedom EVOlyzer or Thunderbolt®.

All products are only available for sale to laboratory professionals and may not be available in all countries. Availability and regulatory status may vary across regions depending on local country-specific registration. Please always read and follow the instructions for use. 

All of our assays have been designed and manufactured to meet the highest global regulatory requirements and quality standards. Tecan is certified under ISO 9001:2015, ISO 13485:2016 and is audited by a notified body according to Medical Device Single Audit Program (MDSAP).

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This is who we are.

As part of the Tecan Group, we have a leading market position in diagnostics and research, with over 40 years of experience in the development, manufacture and supply of enzyme-, radiolabel- and luminescence-based immunoassays.

Our range of high-quality immunoassays is supported by a diverse portfolio of automated solutions, making us the perfect partner for you and your customers.

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At Tecan, we are driven to improve people’s lives and health.