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BAC Clones
BAC Clones
Place of Origin:
United States
Brand:
Empire Genomics
Model:
Supplier:
Empire Genomics
Price:
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1773 
Updated:
8/23/2013
  • Product Detail
  • Company Profile

     Through the RPCI BAC and PAC clone resource, Empire Genomics has access to the RPCI-11 human BAC library, RPCI-22, and -23 mouse BAC libraries in addition to all other RPCI libraries, representing a total of 9 model organisms. These genomic libraries are available for clone selection, characterization, mapping, and distribution to researchers across the globe. Since several of the clones have been sequenced, mapped by the International Human Genome Sequencing Consortium and are included as validated elements on the EG BAC arrays, they have proven to be optimal tools for Fluorescence In Situ Hybridization (FISH) and transgenic studies in mice.

     
    To search for a BAC clone that covers your specific region of interest, click here.
     
    For more information on our BAC clones specification, please read our BAC Clone Specification PDF.
    For our BAC Material Safety Data Sheet Click Here.
     
    Please begin by selecting the number of clones you would like to purchase. After you add this item to your cart, you will be prompted to download an excel template which will allow you to enter specific information about your clones. Please have the following information ready:
    • Clone Library (ie: RPCI-11)
    • Clone Name (ie: 29B01)
    • Format (DNA or Agar Stab)
    • Researcher's Name

     

     

     

    bio-equip.cn
    The leading supplier of molecular diagnostics for customization and production of FISH probes, aGCH assays and upcoming new technologies to be used by Reference labs, Academic labs, Pharma, CRO’s
    and Pharma /Biotech companies around the world.

    Our companion Diagnostics will allow you to :
    -Validate Bio-markers (signature identification and resistance).
    -Identify and qualify the aberration at the Chromosomal level of specific population.
    -Follow up the result of therapeutic treatment (monitoring, compound profiling, drug response, patient stratification and safety)
    -Compare with the result of your current technology.
    -Be translated into the initial phase of your diagnostics development toward new FDA filings (pre-clinical through clinical trial development).
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