Molecular Biology
Nucleic Acid Extraction
Nucleic acid extraction can be tedious and time-consuming. Free up your bench time and let Innovate Life Sciences, accelerate your DNA & RNA extractions. GLP-Compliant Services are also available.
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Nucleic Acid Quantification
From gene expression and genotyping to copy number variation (CNV) analysis and viral titer, we offer a versatile polymerase chain reaction (PCR) portfolio that can be tailored to support the needs of your genomics project.
- Quantitative PCR (qPCR)
qPCR is the tried-and-true method for real-time detection of nucleic acid sequences, providing high-throughput analysis for speed and scalability. No matter the size of your sample concentrations, this method offers a wide detection range of target sequences. Select from convenient and affordable predeveloped assays or partner with our assay experts to design a custom assay to meet your project requirements.
- Key Applications :-
- Gene expression
- Copy number variation (with standard curve)
- Confirmatory testing of NGS data
- SNP genotyping and allelic discrimination
- Methylation analysis (CpG)
- Pathogen detection and quality control
- Customized qPCR solutions
New To Our PCR Portfolio
- Digital PCR (dPCR):
Detect your target sequences with unmatched accuracy dPCR and provide absolute quantitation of nucleic acid sequences without the need for complex standard curves or reference targets.
Through micro reactions, dPCR is highly sensitive for increased detection of rare transcripts and low-frequency targets. This endpoint method is optimal for reproducibility and offers straightforward data analysis and interpretation of your results.
- Key Applications :-
- Absolute copy number variation (CNV)
- Rare mutation and allelic discrimination
- Low-abundance transcript detection
- Viral titer (copies/mL)
- Vector copy number (copies/genome)
- Circulating tumor DNA (ctDNA) and cell-free DNA (cfDNA) detection in liquid biopsy
- PCR for Clinical Research
Regulatory guidelines recommend the use of PCR methodology for multiple quality and safety checkpoints throughout the drug development process. For cell and gene therapy products, hyper-sensitive dPCR has largely been used for the evaluation of viral titer as well as quantification of viral vector copy number (VCN) of treated cells for AAV, lentivirus, and retrovirus.
Contact us to learn how our customized PCR solutions can help you advance your clinical research.
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- Whether through endpoint or real-time detection, our unmatched quantitative PCR (qPCR) or digital PCR (dPCR) capabilities provide you with precise, rapid quantitation of nucleic acid sequences to simplify and advance the path toward your next breakthrough
Sanger Sequencing
Sanger Sequencing is a cost-effective method for determining the nucleotide sequence of DNA. ILS provides high-quality results, industry-leading customer service and fast turnaround times at competitive prices
Customize your Sanger sequencing experience with PCR + Sanger solutions from the leader in DNA sequencing. This fully customizable service allows you to streamline your workflow and extend your bench with your choice of PCR plus Sanger services with accelerated delivery times.
We are well-equipped to handle DNA sequencing of all complexities including single tube, high-throughput, direct bacterial colony, glycerol stock, CLIA, or GLP DNA sequencing projects.
Our mission is to eliminate bottlenecks, improve productivity, and advance your research progress
We support a wide range of applications including targeted microbial/fungal sequencing, NGS data confirmation, antibody heavy/light chain sequencing, mutation detection analysis, cell bank characterization, SNP genotyping and more.
DNA sequencing read lengths up to ~1000 bases.A typical read will provide 800 bases Phred20. Quality Score and Contiguous Read Length (CRL) provided in each read
Our highly-trained team of Sanger sequencing specialists proactively communicate updates, while providing technical expertise on projects big and small.
Contact us to pick-up service for free shipping.
Our proprietary technologies allow for consisent, reliable data even on the most difficult templates (including hairpins and GC-rich DNA).
a wide selection of Universal Primers are available for most standard vectors.
Benefits:
SNP Genotyping Analysis and Detection
SNP analysis and identification are crucial for understanding how individuals might react to certain medications, their vulnerability to environmental factors, and their risk of developing diseases. SNPs also play a significant role in tracking the inheritance of disease genes within families, offering insights into genetic linkages.
ILS specializes in Sanger sequencing-based SNP genotyping, catering to both small-scale studies and extensive research projects. This method can serve as a primary tool for SNP analysis and detection, or as a means to verify results obtained from next-generation sequencing and microarray analyses.
Rely on the expertise of ILS’s Sanger sequencing professionals to propel your SNP genotyping research forward with efficiency, excellence, and dependability.
