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Related Concept Videos

Immunoprecipitation01:20

Immunoprecipitation

Immunoprecipitation, or IP, is a widely used technique that employs protein-antibody interactions to isolate proteins or protein complexes in their native state for studying protein-protein interactions, quaternary structures, or supramolecular complexes. Various modifications of the technique, including chromatin IP, cross-linking IP, and fluorescence IP, are commonly used.
Chromatin Immunoprecipitation
Chromatin immunoprecipitation, also known as ChIP, is used to study protein-DNA or...
Antimicrobial Proteins01:23

Antimicrobial Proteins

Antimicrobial proteins are important components of the immune system. They aid the body in combating pathogens by either killing them directly or hindering their replication processes. Four main types of antimicrobial substances are interferons, the complement system, iron-binding proteins, and antimicrobial proteins.
Interferons
Interferons (IFNs) are proteins produced by lymphocytes, macrophages, and fibroblasts infected with viruses. While IFNs cannot prevent viruses from entering and...
Inhibitors of Bacterial Protein Synthesis01:25

Inhibitors of Bacterial Protein Synthesis

Aminoglycosides constitute a highly potent class of bactericidal antibiotics that exert their antimicrobial effects by targeting the bacterial ribosome, specifically disrupting protein synthesis. These polycationic molecules consist of amino-modified sugars linked via glycosidic bonds to an aminocyclitol core such as 2-deoxystreptamine or streptamine. Their strong positive charges facilitate tight binding to the negatively charged phosphate backbone of ribosomal RNA (rRNA), primarily at the 16S...
Types of Coprecipitation01:10

Types of Coprecipitation

Coprecipitation is the contamination of a precipitate by otherwise soluble species and occurs via different processes. In colloidal precipitates, coprecipitation occurs via surface adsorption. For instance, barium sulfate has a primary layer of adsorbed barium ions and a secondary layer of nitrate counterions. This results in contamination of the precipitate by barium nitrate.
Sometimes, ions in a crystal lattice can undergo isomorphous replacement by inclusions of similar charge and size. For...
Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors01:20

Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors

Antiplatelet drugs emerge as frontline defenders against the insidious threat of thromboembolic diseases, where abnormal clots obstruct vital blood vessels. These drugs stand as bulwarks, inhibiting platelet aggregation and clot formation, thereby mitigating the risk of life-threatening conditions like myocardial infarction, coronary artery disease, and thrombotic strokes.
Prostaglandin synthesis inhibitors, exemplified by the widely known aspirin, wield their power by irreversibly acetylating...

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High-throughput Identification of Bacteria Repellent Polymers for Medical Devices
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Published on: November 5, 2016

PCR inhibitors - occurrence, properties and removal.

C Schrader1, A Schielke, L Ellerbroek

  • 1Food Hygiene and Safety Concepts, Federal Institute for Risk Assessment, Berlin, Germany.

Journal of Applied Microbiology
|July 4, 2012
PubMed
Summary

Polymerase chain reaction (PCR) is a key method for detecting genetic material, but inhibitors in samples can cause false negatives. This review covers PCR inhibitor properties, occurrence, and removal strategies for accurate results.

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Area of Science:

  • Molecular Biology
  • Analytical Chemistry
  • Microbiology

Background:

  • Polymerase chain reaction (PCR) is a standard technique for detecting microorganisms and genetic markers.
  • PCR assays can be negatively impacted by inhibiting substances present in various sample types.
  • These inhibitors can reduce assay sensitivity and lead to inaccurate, false-negative results.

Purpose of the Study:

  • To review the general properties and diverse mechanisms of action of PCR inhibitors.
  • To discuss the occurrence of PCR inhibitors in specific sample matrices.
  • To present and evaluate strategies for removing PCR inhibitors and quality control methods.

Main Methods:

  • Literature review focusing on PCR inhibitor properties and sample matrices.
  • Analysis of various nucleic acid preparation protocols for inhibitor removal.
  • Discussion of quality control measures to assess inhibitor influence on PCR.

Main Results:

  • PCR inhibitors are a diverse group of substances with varied properties and actions.
  • Specific sample types often contain characteristic PCR inhibitors, requiring tailored preparation methods.
  • Effective removal strategies and quality control assessments are crucial for reliable PCR outcomes.

Conclusions:

  • Understanding PCR inhibitor characteristics is vital for optimizing detection assays.
  • Matrix-specific sample preparation is essential to mitigate inhibition.
  • Implementing robust removal and quality control strategies ensures the accuracy of PCR-based analyses.