DNA Aptamer Library Kit

DNA Aptamer Library Kit

$1,989.00

The DAL-01 DNA Aptamer Library Kit provides pre-validated ssDNA library oligos and optimized primers to streamline your in vitro selection (SELEX) workflows. Designed for high-efficiency amplification on Capture SELEX or magnetic bead platforms, this kit includes single-stranded DNA library pools (N62 or N40) and modified primers (FAM, Biotin, Phosphorylation) to support 2–4 independent aptamer discovery projects without upfront optimization.

Product Overview

The Fusion BioLabs DNA Aptamer Library Kit (DAL-01) provides pre-validated ssDNA library oligos and optimized primers to streamline your in vitro selection (SELEX) workflows. Designed to bypass time-consuming library construction and amplification optimization, this kit contains sufficient reagents to perform 2 to 4 independent aptamer development projects (including primary library setup for Round 1 SELEX and secondary library amplification across iterative rounds), depending on your specific experimental design.

DAL-01 DNA Aptamer Library Structure

Performance Specifications

Binding Affinity

Nanomolar

High-specificity target recognition across diverse targets.

Throughput

6–12 Rounds

Typical iterative selection cycle for pool enrichment.

Storage

-20°C

Shipped on blue ice; stable for 12 months stored properly.

Key Features

  • High Efficiency Amplification: Designed and optimized for rapid, specific amplification during SELEX rounds on both Capture SELEX and traditional magnetic bead-based platforms.
  • Versatile Strand Separation: Compatible with multiple single-stranded DNA (ssDNA) generation protocols, allowing flexible integration into your lab’s preferred workflow:
    • Lambda Exonuclease Digestion: Utilizes 5′-phosphorylated reverse primers for enzymatic digestion.
    • Alkaline Denaturation: Utilizes 5′-biotinylated reverse primers with streptavidin-coated magnetic beads.
  • Fluorescent Tracking: Includes a 5′-FAM labeled forward primer for downstream quantification and binding monitoring via fluorescence.
Handling & Preparation Best Practices

Always heat-denature the primary library at 95°C for 5 minutes and immediately snap-cool on ice or room temperature buffer prior to Round 1 selection. This ensures proper secondary structure formation for target binding.

Library Pool Structures

The kit is available with two random region configurations:

SKU Option Forward Primer Random Region Reverse Primer Total Length
DAL-01 (N62) 19 bp N62 (62 nt) 19 bp 100 nt
DAL-01 (N40) 18 bp N40 (40 nt) 20 bp 78 nt

Kit Components

All components are supplied in liquid format:

Vial Component Concentration Volume
1 ssDNA Library Oligos (N62 or N40) 100 µM 30 µL
2 Unmodified Forward Primer 100 µM 30 µL
3 5′-FAM Labeled Forward Primer 100 µM 30 µL
4 Unmodified Reverse Primer 100 µM 30 µL
5 5′-Phosphorylated Reverse Primer 100 µM 30 µL
6 5′-Biotinylated Reverse Primer 100 µM 30 µL

Protocol Flowchart

Flowchart of Magnetic Beads-Based SELEX Technology

N62 or N40 ssDNA Library Random sequences flanked by constant regions (19/18 bp Forward primer & 19/20 bp Reverse primer) 5' 3' Target Molecule Immobilized on Magnetic Nanoparticles (MNP) Binding of Aptamers with Target on MNP Magnetic Separation Unbound Library (Discarded) Target-Bound Pool PCR Amplification ssDNA Generation Option 1: λ Exonuclease Digestion (Selective 5'-phosphorylated strand digestion) Option 2: Streptavidin Magnetic Beads & Alkaline Denaturation (NaOH) (Biotin-labeled antisense strand separation) Next Round Pool Repeat 6–12 Cycles Enriched Selected Aptamers (Last Round) Traditional Path Cloning Sanger Sequencing High-Throughput Path NGS Sequencing Bioinformatics Analysis Candidate DNA Aptamers

Applications

  • Primary ssDNA library construction for Round 1 SELEX.
  • Secondary library amplification across iterative SELEX selection cycles.
  • Aptamer candidate discovery using magnetic bead, microfluidic, or capture-based selection methods.
Weight 0.5 lbs
Dimensions 1 × 1 × 1 in
Random Region Length

N62 (62 nt Random), N40 (40 nt Random)

DOCUMENTATION

Data Sheet                                                                                                Magnetic Beads-based SELEX Protocol

Aptamer Development Services

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Magnetic beads-based SELEXFind DNA/RNA Aptamers against Targets Immobilized on Magnetic BeadsLearn More
Capture-SELEXFind DNA/RNA Aptamers Using Immobilized Aptamer LibraryLearn More
Cell-SELEXIdentify either Cell-Surfaced or Cell-Internalized DNA/RNA Aptamers Learn More
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