Asuragen – QuantideX BCR-ABL
Asuragen’s Precision Oncology Solutions.
Revolutionising Precision Oncology with QuantideX®: Where Sensitivity Meets Scalability
Asuragen’s Precision Oncology Solutions.
Revolutionising Precision Oncology with QuantideX®: Where Sensitivity Meets Scalability
THESE PRODUCTS ARE NOT AVAILABLE FOR PURCHASE BY THE GENERAL PUBLIC.
How is your lab performing FMR1 gene testing?
THESE PRODUCTS ARE NOT AVAILABLE FOR PURCHASE BY THE GENERAL PUBLIC.
Cystic fibrosis (CF) is a life-limiting, autosomal recessive disease caused by the presence of pathogenic alterations in the CFTR gene.
THESE PRODUCTS ARE NOT AVAILABLE FOR PURCHASE BY THE GENERAL PUBLIC.
With the AmplideX Trio, you can use one shared workflow to analyze CFTR, SMN1/2, and FMR1. This saves your lab tech time, simplifies training, and reduces consumables used.
Products are for professional/laboratory use only.
The AmplideX® PCR/CE SMN1/2 Plus Kit* is an in vitro nucleic acid amplification kit intended to aid in the screening of carriers for and diagnosis of spinal muscular atrophy (SMA).
Products are for professional/laboratory use only.
Webinar Invitation:
Looking Beyond Copy Number:
Broad SMN1 and SMN2 profiling in under four hours with the AmplideX® PCR/CE SMN1/2 Plus Kit (RUO)
Products are for professional/laboratory use only. Abacus dx is pleased to announce the launch of the latest assay from the Asuragen spinal muscular atrophy (SMA) portfolio – AmplideX® PCR/CE SMN1/2 Plus Kit*.
Products are for professional/laboratory use only.
The AmplideX® PCR/CE HTT kit simplifies the detection and sizing of the CAG trinucleotide repeats in the HTT gene by overcoming the challenges of adjacent SNPs and variable CAG repeats which can complicate primer binding and cause allele dropouts.
Products are for professional/laboratory use only.
The AmplideX® suite of products is designed to solve unmet testing needs in inherited genetic disorders. The technology overcame a 20-year challenge by reliably amplifying the FMR1 gene. This allowed researchers to gain a deeper understanding of fragile X syndrome, the most common known inherited cause of intellectual disability and autism.