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genetic disease, genetic engineering,  custom chip design, genotyping services, human  high-throughput genotyping, microarray design, genome, Apex,  development, arrayed primer extension, SNP,  genomics, genetic testing services, SNP tests, DNA chip, arrayed primer extension, microarray scanner, p53,  drug development,  diagnostics, personalized  treatment, human medicine, SNP, biotechnology, technology transfer, gene, DNA test

NEWS of 2005

12.2005 Asper Biotech announces the release of its next  DNA test 
  
The HEREDITARY HEARING LOSS test (HHL  DNA  test). The new test is a single assay, which enables comprehensive mutation detection in a number of genes linked to HHL. The test covers 201 mutations in multiple genes that underlie both nonsyndromic (Connexin 26, Connexin 30, Connexin 31, Connexin 43, SLC26A4, SLC26A5, 12SrRNA, and tRNA Ser) and certain syndromic (Cx26 and SLC26A4) causes of hearing loss. Asper's hereditary hearing loss test has been extensively validated by pre-screened patient DNA samples in a well-designed blind study. As our previous published studies have shown, our tests are able to detect more than 98% of the existing genetic variations, so it's well suited for screening of known mutations related to hereditary hearing loss. The development and validation of the HHL test has been a joint work between Asper Biotech and Stanford University. For further information please look http://www.asperbio.com/HHL.htm or contact info@asperbio.com.

10.2005 Thalassemia assay updated, and the number of mutations screened for was increased to 46
  
One of the most validated test at Asper Biotech, the Thalassemia assay has been updated by adding 9 new mutations to the test. The current test version covers 40 mutations from beta-globin and six mutations from delta-globin genes. This update was the first one from the major upgrade program, which will be followed by additional updates to present mutations from different globin genes. The recent update was conducted in collaboration with The Cyprus Institute of Neurology and Genetics.
For further questions please contact Asper Biotech
info@asperbio.com

09.2005 New publication has been published:
  

Zernant J, Kulm M, Dharmaraj S, den Hollander AI, Perrault I, Preising MN, Lorenz B, Kaplan J, Cremers FP, Maumenee I, Koenekoop RK, Allikmets R., Genotyping microarray (disease chip) for leber congenital amaurosis: detection of modifier alleles.
Invest Ophthalmol Vis Sci. 2005 Sep;46(9):3052-9.
  

08.2005 New publication co-authored by Asper Biotech's Scientists has been published:
  

Schrijver I, Oitmaa E, Metspalu A, Gardner P.
Genotyping Microarray for the Detection of More Than 200 CFTR Mutations in Ethnically Diverse Populations. J Mol Diagn. 2005 Aug;7(3):375-87
  

07.2005 New publication co-authored by Asper Biotech's Scientists has been published:
 

Le Calvez F, Ahman A, Tonisson N, Lambert J, Temam S, Brennan P, Zaridze DG, Metspalu A, Hainaut P.
Arrayed Primer Extension Resequencing of Mutations in the TP53 Tumor Suppressor Gene: Comparison with Denaturing HPLC and Direct Sequencing.
Clin Chem. 2005 Jul;51(7):1284-7.

  

04.2005 Asper Biotech's branch Asper Ophthalmics invites all interested to its booth (#219) at the ARVO 2005 in Fort Lauderdale, Florida, USA, on May 1-4.
 
Asper will be represented at meeting of the Association for Research in Vision and Ophthalmology (ARVO) 2005. The meeting will be held in Fort Lauderdale, Florida, USA on 1- 4 of May. Asper welcomes all existing partners and everyone interested in collaborating with Asper to attend the conference and meet in its booth #219. 
  

02.2005 Asper plans launching five new tests in Q1 and Q2 2005

Asper continues to establish and validate genetic tests targeting different research and clinical areas. First version of Central nervous system (CNS) chip is currently under development. CNS test will become available during Q1 and it would be established as an open assay, whereby researchers are free to customize the chip by including additional SNPs to already existing set of markers. In couple of months Asper will launch a similar test for screening a variety of SNPs from ABC Transporter genes. Later this year several other tests will follow. For further questions please contact info@asperbio.com
  

01.2005  Asper launches new website
  
As Asper is focusing its efforts on genetic testing, a new updated website was launched. The website should provide initial information about the tests as well as describe how to prepare and ship the samples for high quality analysis. In addition for keeping our current customers and partners updated about the latest news Asper plans to launch a concentrated newsletter in Q1. For further questions please contact info@asperbio.com
  

GENETIC TESTS

   Thalassemia testing

   Hereditary Hearing Loss
    testing

   Cystic Fibrosis testing

   DNA repair testing

   Ashkenazi Jewish (AJ)
    diseases testing
 
   Wilson Disease testing
   
   Hereditary Breast and
    Ovarian Cancer testing

   Stargardt disease, age
   
related macular 
    dystrophy, cone-rod
    dystrophy testing

   Usher syndrome testing
 
   Leber congenital
    amaurosis (LCA) genetic
    testing        
 
   Autosomal recessive
   
retinitis pigmentosa 
    (AR-RP) genetic testing

   Autosomal dominant
   
retinitis pigmentosa 
    (AD-RP) genetic testing
  
   Bardet Biedl syndrome
    (BBS) genetic testing

   Autosomal dominant
   
optic atrophy testing 

   Corneal dystrophy
   
testing 

   Congenital stationary
   
night blindness 
    genetic testing

    Vitelliform macular
    dystrophy testing

MICROARRAY SLIDES

   Genorama® SAL

  Genorama® SA
  

 

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