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Manufactured by BioVendor

fastGEN CFTR 8-kit

  • Regulatory status:RUO
  • Type:Demo kit
  • Other names:CFTR, Cystic Fibrosis Transmembrane Conductance Regulator
  • Species:Human
Cat. No. Size Price


New RDNGS0006A for 8 samples (1 kit)
PubMed Product Details
Technical Data

Try Demo kits of CFTR

In the case of demo kits, our application specialist will come to your laboratory, guide you through the entire sample preparation and help you analyze the results in our GENOVESA bioinformatics software.

Are you interested in more? Contact our product manager:

Iveta Tóthová, PhD.
Product & Scientific Manager
Phone: +420 724 873 015
E-mail: tothova@biovendor-mdx.com

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.

Visit GENOVESA

Type

Demo kit

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 overall
  • It provides an examination of the mutation status of samples (DNA) by ultra-deep sequencing
  • Assay format is 32 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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