AdnaNews Vol 1, issue 2

26th November

» Read AdnaNews – Learn more about AdnaGen’s CE-certified kits and latest research in CTC profiling

» Information about AdnaGen Kits

CTC_Bead

European Life Science Awards

22nd November

Nominate candidates for the European Life Science Awards!

» Entry Form

Stem cell report

18th November

» GEN Reports: Stem Cells Market Trends based on Primary Industry Analysis

» More market reports

Postdoc position

18th November

Postdoc position opportunity at University of Skövde in collaboration with TATAA

» Postdoc in Biomedicine 2013

» Information about TATAA Core Facility services

TATAA Seminar – BioMark applications

15th November

“MIQE-guidelines and Validation of qPCR Experiments for BioMark Applications”

TATAA seminar by Robert Sjöback, PhD

Venue: Belfragesalen, BMC D15, Bio Medicine Center (BMC), Lund University, Klinikgatan 22184
Date and time: November 26, 2013; 15.30 hrs to 16.30 hrs

 

Webcast: Single cell analysis

15th November

» “High Throughput Technologies for Single Cell Genetic Analysis” by Richard Mathies

» CelluLyser™ for direct single cell lysis – the ultimate RNA preparation for single cell profiling

» TATAA GrandMaster PreAmp Mix – The most powerful preamplification master mix on the market

PCR in-depth focus

15th November

» “PCR in-depth focus”

• Challenges for qRT-PCR in detecting / quantifying microRNA in vitro and in vivo

• Emerging clinical applications of digital PCR

• Workshop Preview: Advanced 3d cell based assays, preparation, analysis and troubleshooting

 

» TATAA quality assessment tools

» TATAA CSO

PCR 30 years

14th November

Read “PCR @ 30: 30 Years Young and Still Evolving” by Mikael Kubista in GEN and interview of Kary Mullis, the inventor of PCR.

 

After specializing in qPCR for more than a decade TATAA Biocenter now introduces its own series of mixes for optimal and high quality results. Our mission is to deliver a reagent series that provides superior qPCR performances in a variety of applications and throughout the entire qPCR workflow.

» TATAA GrandMaster Mastermixes

» TATAA GrandScript cDNA Synthesis kits

» TATAA GrandMaster PreAmp Mastermix

Single cell lysis

14th November

TATAA publishes on single cell lysis in Frontiers in Oncology

» Direct cell lysis for single-cell gene expression profiling

 

» TATAA GrandMaster PreAmp – the most efficient preamplification mix on the market

» TATAA Cellulyser for single cell lysis

» TATAA Universal RNA Spike – evaluate the performance of the lysis buffers and RT efficiencies

 

Meet TATAA in Stockholm

6th November

Take the opportunity to talk to us about qPCR!

We will help you to get the most out of your qPCR experiments by introducing our services, products and courses, and we are happy to discuss any questions you may have regarding the entire qPCR workflow.

Stockholm, December 5-6, 2013 at Karolinska Institutet

Time: December 5: 8:30 AM-5:30 PM
December 6: 8:30 AM-1:30 PM

» Program – Biosience 2013

» Website – Bioscience 2013

Do not miss – presentation by Dr. Mikael Kubista, founder and CEO of TATAA Biocenter

Taking Expression Profiling to New Levels

Mikael Kubista

qPCR is developing into the most powerful platform to profile samples extracting the biologically relevant information. Major breakthroughs in recent years include the development of highly accurate methods for the profiling of various biomolecules including mRNA, microRNA, lncRNA and protein, combined with robust preamplification methods that allow the profiling of large number of markers starting with minute sample amounts, including single cells.

In my talk I will present some of the most recent tools and illustrate the approaches by presenting the first single cell multiway study, where response to brain trauma in mice is studied over time using single cell expression profiling, the first single cell multianalyte profiling study, where DNA, mRNA, microRNA, lncRNA and protein are measured in the same cell, and qPCR tomography to measure intracellular mRNA gradients that lead to asymmetric cell division.