Latest NewsSeptember 22, 2026
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Why pH, temperature and ions belong in the design specification
The same aptamer sequence works reliably in one laboratory and produces a weak signal in another. Has something gone wrong with the DNA? Perhaps. But first ask whether the two laboratories have given the molecule the same chemical environment.

An aptamer is a short strand of DNA or RNA that recognizes a molecular target through its three-dimensional arrangement and chemical contacts. Unlike a rigid manufactured component, it can change shape. Experiments that track individual aptamers show that ions can alter the balance between those shapes without changing a single nucleotide – the building block of the strand.

Sequence defines the possibilities. The environment helps determine which states are populated, which contacts are favorable and whether productive binding can occur. Operating conditions therefore belong in the design specification.






Science Behind|Blog post|20 mins read
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Science Behind
Blog post

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Why pH, temperature and ions belong in the design specification
pH, temperature and ion composition shape how an aptamer folds, binds and performs. Discover why final assay conditions must be part of the design specification from the start.
September 22, 2026
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Visionary Vision
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Why Protein Structure
Is Becoming
Design-Ready Now
AI protein models, structural sampling and experimental restraints are making protein structures more useful for molecular design. Learn how models can improve virtual screening and discovery.
September 8, 2026
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Tips & Tricks
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Why change the chemistry of aptamers?
A chemical modification can protect an aptamer, change its structure, alter its binding surface or reshape its pharmacokinetics. The right modification therefore has to be chosen...
August 25, 2026
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Visionary Vision
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The targeting layer is a design variable
A conventional small molecule has to do everything at once. One chemical structure supplies potency, solubility, stability, permeability, distribution and clearance and those properties are entangled.
August 11, 2026
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Science Behind
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No antibody? You may not have to build the assay from scratch
Many protein assays and immunoassays are built around antibodies. Sometimes the antibody is the part you cannot get. The target is too similar across species to raise a useful immune response.
July 30, 2026
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Tips & Tricks
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How to choose the right binding site for your aptamer
An aptamer can hit its target at single-digit nanomolar and still be useless. The site it found gets buried when the protein joins its complex.
July 21, 2026
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The proteome doesn't have a coverage gap - it has a coverage bias
We can now measure thousands of proteins in a drop of blood. The ones we still can't measure aren't a random remainder – and that bias shapes what medicine can find.
July 14, 2026
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Xelari Platform Update: A Refined Experience, a New Visual System, and More Candidates
We have rebuilt the Xelari experience around how it is actually used: cleaner workflows, a new visual system called Cold Mineral, and more candidates delivered on every plan. The update is live now.
June 22, 2026
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Research paper

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Evaluation of Artificial Intelligence-Generated DNA Aptamers Against Treponema pallidum Surface Proteins
DNA aptamer sequences were selected in silico with assistance from artificial intelligence (AI) using the new Xelari.com platform against three known immunogenic surface proteins of Treponema pallidum
February 6, 2026
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Research paper

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Aptamer Design: From SELEX to AI-Driven Rational Design
A technical overview of modern affinity reagent design – aptamers, chemical antibodies, and computational molecular binders.
December 11, 2025
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Research paper
Winner

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AliNA – a deep learning program for RNA secondary structure prediction
Classical thermodynamic folding ignores the specificity of biological folding; conventional deep-learning methods inherit homology bias from their training sets.
September 14, 2023
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