Expression cloning

Results: 111



#Item
1Molecular cloning, sequence characterization, and gene expression profile of a novel water buffalo (Bubalus bubalis) gene: Na+, K+-ATPase β2-subunit (ATP1B2)

Molecular cloning, sequence characterization, and gene expression profile of a novel water buffalo (Bubalus bubalis) gene: Na+, K+-ATPase β2-subunit (ATP1B2)

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Source URL: doi.fbn-dummerstorf.de

- Date: 2014-08-05 05:14:04
    2  	
   Transfection	
  and	
  Subsequent	
  Transduction	
  Protocols	
  for	
  Single	
  shRNA	
  Expression	
   Constructs	
  From	
  TRC1,	
  1.5,	
  or	
  2	
  Library	
  Clones	
   	
  

        Transfection  and  Subsequent  Transduction  Protocols  for  Single  shRNA  Expression   Constructs  From  TRC1,  1.5,  or  2  Library  Clones    

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    Source URL: functionalgenomicsfacility.org

    Language: English - Date: 2015-08-26 12:58:22
    3The MultiBac BEVS for producing proteins and their complexes (Prot54)  The MultiBac BEVS for producing proteins and their complexes (Prot54)  Frederic Garzoni, Christoph Bieniossek and Imre Berger

    The MultiBac BEVS for producing proteins and their complexes (Prot54) The MultiBac BEVS for producing proteins and their complexes (Prot54) Frederic Garzoni, Christoph Bieniossek and Imre Berger

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    Source URL: www.epigenesys.eu

    Language: English - Date: 2016-05-10 10:16:09
    4IFAFS Project Milestones  Pituitary Breast

    IFAFS Project Milestones Pituitary Breast

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    Source URL: cogburn.dbi.udel.edu

    Language: English - Date: 2002-04-18 02:22:00
    5CRB-FUNDED RESEARCH PROGRESS REPORT Figure 1. In order to find nucleotide variability at both ends (3’ and 5’) of CTV California strain genome (highlighted in gray), the virus RNA has to be converted to a double-stra

    CRB-FUNDED RESEARCH PROGRESS REPORT Figure 1. In order to find nucleotide variability at both ends (3’ and 5’) of CTV California strain genome (highlighted in gray), the virus RNA has to be converted to a double-stra

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    Source URL: citrusresearch.org

    Language: English - Date: 2016-02-24 20:49:09
    6Yeast Two-Hybrid Procedure 1. Generate a GAL4 DNA-BD fusion by cloning the gene of interest in frame with the GAL4 DNA binding domain of pGBKT7. 2. Transform AH109 with bait plasmid, detect bait expression and test for a

    Yeast Two-Hybrid Procedure 1. Generate a GAL4 DNA-BD fusion by cloning the gene of interest in frame with the GAL4 DNA binding domain of pGBKT7. 2. Transform AH109 with bait plasmid, detect bait expression and test for a

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    Source URL: hanlab.xmu.edu.cn

    Language: English
    7Frequently Asked Questions (CCSB LentiORF) General Information about CCSB-Broad Lentiviral Expression Library Disclaimer The Functional Genomics Facility is a distributor of LentiORF (clone ID. eg. ccsb304_xxxx) collecti

    Frequently Asked Questions (CCSB LentiORF) General Information about CCSB-Broad Lentiviral Expression Library Disclaimer The Functional Genomics Facility is a distributor of LentiORF (clone ID. eg. ccsb304_xxxx) collecti

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    Source URL: functionalgenomicsfacility.org

    Language: English - Date: 2015-09-01 12:01:26
    8   Adaptation	
  of	
  the	
  pET-­‐Duet	
  expression	
  system	
  to	
  USER-­‐Fusion	
   based	
  cloning	
  -­‐	
  using	
  statin	
  biosynthesis	
  as	
  a	
  case	
  study	
   Malgorzat

      Adaptation  of  the  pET-­‐Duet  expression  system  to  USER-­‐Fusion   based  cloning  -­‐  using  statin  biosynthesis  as  a  case  study   Malgorzat

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    Source URL: files.conferencemanager.dk

    Language: English - Date: 2016-05-26 10:36:48
      9DNA cloning for protein expression using Gateway© technology Artem Evdokimov  1. Reagents & their properties. Storage & propagation of Gateway components. Helpful things to be aware of regarding storage a

      DNA cloning for protein expression using Gateway© technology Artem Evdokimov 1. Reagents & their properties. Storage & propagation of Gateway components. Helpful things to be aware of regarding storage a

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      Source URL: www.xtals.org

      Language: English
        10A PCR-based strategy for cloning short hairpin sequences: “PCR SHAGging”. Our overall approach is to use an RNA polymerase III promoter to drive expression of encoded short hairpin RNA (shRNA). For this purpose we us

        A PCR-based strategy for cloning short hairpin sequences: “PCR SHAGging”. Our overall approach is to use an RNA polymerase III promoter to drive expression of encoded short hairpin RNA (shRNA). For this purpose we us

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        Source URL: hannonlab.cshl.edu

        Language: English - Date: 2008-06-12 19:01:47