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Manufactured by BioVendor

fastGEN CFTR 24-kit

  • Regulatory status:RUO
  • Type:NGS - Next generation sequencing
  • Other names:CFTR, Cystic Fibrosis Transmembrane Conductance Regulator
  • Species:Human
Cat. No. Size Price


New RDNGS0005 for 24 samples (1 kit)
PubMed Product Details
Technical Data

Bioinformatic analysis software: GENOVESA

The GENOVESA fastGEN software module, available online, can to be used to analyse sequencing data. It is a cloud all-in-one solution for the analysis of raw data (FASTQ format files) with technical and application support.

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Type

NGS - Next generation sequencing

Description

Compatible with MiSeq and NovaSeq sequencers, for other platforms use conversion kit.

Reconstitution

No

Applications

Isolated DNA

Sample Requirements

5 µl/well

Shipping

At -20°C temperature. Upon receipt, store the product at the temperature -20°C.

Storage/Expiration

Store the complete kit at -20°C. Under these conditions, all components are stable until the expiration date (see label on the box).

Note


BioVendor Group fastGEN: A breakthrough system for one-step NGS library

Summary

Features

  • It is intended for research use only
  • The total assay time is less than <30 min hands on time, < 14h overal
  • It provides an examination of the mutation status of samples (DNA isolated ) by ultra-deep sequencing
  • Assay format is 96 tubes (4 tubes for one DNA sample) with Master Mixes
  • Components of the kit are provided ready to use
  • The simplicity of the fastGEN method is into mix one particular Master Mix with a DNA sample and insert it into a thermocycler.

Research topic

Others

Summary

Cystic fibrosis (CF) is a multisystem disease with autosomal recessive inheritence, affecting the cystic fibrosis transmembrane conductance regulator (CFTR) gene. CF mainly affects the lungs and pancreas, but also the upper airways, liver, intestine, and reproductive organs.
Currently, more than 2000 germline sequence variants of the CFTR gene have already been identified, though not all result in CF.

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