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AB315068

Clostridium difficile Toxin A + Toxin B ELISA Kit

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Clostridium difficile Toxin A + Toxin B ELISA Kit is a single-wash 90-min Simplestep used to quantify Clostridium difficile Toxin A + Toxin B with a sensitivity of 37.638 pg/ml. The assay uses a simple mix-wash-read protocol with just one incubation and one wash step.

- Colorimetric Sandwich ELISA - 450 nm readout : works on any standard plate reader

View Alternative Names

toxA, tcdA, Toxin A

2 Images
Sandwich ELISA - Clostridium difficile Toxin A + Toxin B ELISA Kit (AB315068)
  • sELISA

Supplier Data

Sandwich ELISA - Clostridium difficile Toxin A + Toxin B ELISA Kit (AB315068)

Recombinant Toxin A + Toxin B was spiked into the following samples and diluted in a 2-fold dilution series in Sample Diluent NS. Undiluted samples are 50% RPMI containing 10%FBS. The interpolated dilution factor corrected values are plotted (mean +/- SD, n=2).

Sandwich ELISA - Clostridium difficile Toxin A + Toxin B ELISA Kit (AB315068)
  • sELISA

Supplier Data

Sandwich ELISA - Clostridium difficile Toxin A + Toxin B ELISA Kit (AB315068)

Example of Clostridium difficile Toxin A + Toxin B standard curve. Background-subtracted data values (mean +/- SD) are graphed.

Key facts

Detection method

Colorimetric

Sample types

Cell culture media

Reacts with

Clostridium difficile

Assay type

Sandwich (quantitative)

Sensitivity

= 37.638 pg/mL

Range

234.375 - 15000 pg/mL

Assay time

1h 30m

Assay Platform

Pre-coated microplate (12 x 8 well strips)

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Reactivity", "Dilution Info", "Notes"] }, "values": { "sELISA": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" } } }

Product details

Clostridium difficile Toxin A + Toxin B SimpleStep ELISA® kit is a single-wash 90 min sandwich ELISA designed for the quantitative measurement of Toxin A + Toxin B protein in Cell culture.

SimpleStep ELISA® technology employs capture antibodies conjugated to an affinity tag that is recognized by the monoclonal antibody used to coat our SimpleStep ELISA® plates. This approach to sandwich ELISA allows the formation of the antibody-analyte sandwich complex in a single step, significantly reducing assay time. See the SimpleStep ELISA® protocol summary in the image section for further details. Our SimpleStep ELISA® technology provides several benefits:

-Single-wash protocol reduces assay time to 90 minutes or less
-High sensitivity, specificity and reproducibility from superior antibodies
-Fully validated in biological samples
-96-wells plate breakable into 12 x 8 wells strips

A 384-well SimpleStep ELISA® microplate (ab203359) is available to use as an alternative to the 96-well microplate provided with SimpleStep ELISA® kits.

Precision

[ { "reproducibilityType": "Intra", "sample": "Supernatant", "replicates": 8, "mean": null, "standardDeviation": null, "coefficientOfVariability": "4.4" }, { "reproducibilityType": "Inter", "sample": "Supernatant", "replicates": 3, "mean": null, "standardDeviation": null, "coefficientOfVariability": "3.7" } ]

Recovery

[ { "sample": "Cell culture media", "range": "104 - 119 %", "average": "= 113" } ]

What's included?

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Properties and storage information

Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
+4°C
Storage information
+4°C

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

Clostridium difficile Toxin A and Toxin B also known as TcdA and TcdB are large glycoproteins secreted by the bacterium Clostridium difficile. TcdA weighs approximately 308 kDa while TcdB is about 270 kDa. These toxins are primarily expressed in the gut following infection by C. difficile. TcdA and TcdB function as exotoxins entering host cells and leading to the disruption of cellular processes by glycosylating small GTPases such as Rho proteins. This modification impairs these proteins' ability to signal causing breakdown of the cytoskeleton and resulting in cell death and inflammation.
Biological function summary

Toxin A and Toxin B damage the intestinal epithelium leading to increased permeability and inflammatory response. These toxins work independently and are not part of a complex although both are essential for C. difficile pathogenicity. TcdA is generally thought to initiate the inflammatory process in the gut mucosa while TcdB is the primary mediator of cytotoxicity. Both toxins contribute to the destruction of tight junctions which leads to disruption of epithelial barrier function.

Pathways

TcdA and TcdB primarily affect the Rho signaling pathway. These toxins inactivate Rho family proteins including Rho Rac and Cdc42 leading to actin depolymerization and loss of cell shape. The Rac pathway also links to pathways that control cell cycling and apoptosis. Through these pathways the toxins alter not only cellular structure but also contribute to signaling cascades that increase apoptosis and inflammatory mediators like cytokines.

Toxin A and Toxin B play central roles in the development of Clostridium difficile infection (CDI) a major cause of antibiotic-associated diarrhea. CDI leads to symptoms such as severe diarrhea and colitis and in the most severe cases pseudomembranous colitis. The toxins' ability to damage intestine linings connects them to inflammation-related proteins like cytokines and chemokines which further exacerbate tissue damage and disease progression. Understanding these toxins' roles can aid in developing targeted therapies that mitigate their harmful effects.

Product protocols

Target data

Toxin A. Precursor of a cytotoxin that targets and disrupts the colonic epithelium, inducing the host inflammatory and innate immune responses and resulting in diarrhea and pseudomembranous colitis (PubMed : 20844489). TcdA and TcdB constitute the main toxins that mediate the pathology of C.difficile infection, an opportunistic pathogen that colonizes the colon when the normal gut microbiome is disrupted (PubMed : 19252482, PubMed : 20844489). Compared to TcdB, TcdA is less virulent and less important for inducing the host inflammatory and innate immune responses (PubMed : 19252482). This form constitutes the precursor of the toxin : it enters into host cells and mediates autoprocessing to release the active toxin (Glucosyltransferase TcdA) into the host cytosol (By similarity). Targets colonic epithelia by binding to some receptor, and enters host cells via clathrin-mediated endocytosis (By similarity). Binding to LDLR, as well as carbohydrates and sulfated glycosaminoglycans on host cell surface contribute to entry into cells (PubMed : 16622409, PubMed : 1670930, PubMed : 31160825). In contrast to TcdB, Frizzled receptors FZD1, FZD2 and FZD7 do not act as host receptors in the colonic epithelium for TcdA (PubMed : 27680706). Once entered into host cells, acidification in the endosome promotes the membrane insertion of the translocation region and formation of a pore, leading to translocation of the GT44 and peptidase C80 domains across the endosomal membrane (By similarity). This activates the peptidase C80 domain and autocatalytic processing, releasing the N-terminal part (Glucosyltransferase TcdA), which constitutes the active part of the toxin, in the cytosol (PubMed : 17334356, PubMed : 19553670, PubMed : 27571750).. Glucosyltransferase TcdA. Active form of the toxin, which is released into the host cytosol following autoprocessing and inactivates small GTPases (PubMed : 22267739, PubMed : 22747490, PubMed : 24905543, PubMed : 30622517, PubMed : 7775453). Acts by mediating monoglucosylation of small GTPases of the Rho family (Rac1, RhoA, RhoB, RhoC, Rap2A and Cdc42) in host cells at the conserved threonine residue located in the switch I region ('Thr-37/35'), using UDP-alpha-D-glucose as the sugar donor (PubMed : 22267739, PubMed : 22747490, PubMed : 24905543, PubMed : 30622517, PubMed : 7775453). Monoglucosylation of host small GTPases completely prevents the recognition of the downstream effector, blocking the GTPases in their inactive form, leading to actin cytoskeleton disruption and cell death, resulting in the loss of colonic epithelial barrier function (PubMed : 7775453). Also able to catalyze monoglucosylation of some members of the Ras family (H-Ras/HRAS, K-Ras/KRAS and N-Ras/NRAS), but with much less efficiency than with Rho proteins, suggesting that it does not act on Ras proteins in vivo (PubMed : 30622517).
See full target information tcdA

Additional targets

tcdB
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