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We narrowed to 79,217 results for: rest

Showing: 5181 - 5200 of 79217 results
  1. pAC-ZEAXipi

    Plasmid
    #53287
    Purpose
    Contains crtE, idi, crtI, crtY, crtB, and crtZ genes of Erwinia herbicola (Pantoea agglomerans) Eho10 and thereby produces zeaxanthin in E. coli
    Insert
    crtE, idi, crtY, crtI, crtB, crtZ
    Use
    Low copy number bacterial cloning vector
    Promoter
    endogenous promoters
    Available since
    Jan. 21, 2015
    Availability
    Academic Institutions and Nonprofits only
    Cited by
  2. pK068.CAG-FRT-stop-FRT-EGFP-ires-tTA-WPRE (Supernova)

    Plasmid
    #85008
    Purpose
    For Flpe/FRT-based Supernova-GFP, pK068 should be used with pK036. The GFP fragment of pK068 can be replaced with another gene by SalI and EcoRV.
    Depositor
    Has service
    50 µg Transfection-Ready DNA and 100 µg Transfection-Ready DNA
    Insert
    EGFP-ires-tTA
    Expression
    Mammalian
    Available since
    Nov. 30, 2016
    Availability
    Academic Institutions and Nonprofits only
  3. pLVX-FLAG-mCherry-C1-centrin-1

    Plasmid
    #73333
    Purpose
    Lentiviral vector encoding centrin-1 with N-terminal FLAG and mCherry tags
    Depositor
    Insert
    centrin-1 (CETN1 Human)
    Use
    Lentiviral
    Tags
    FLAG and mCherry
    Expression
    Mammalian
    Promoter
    CMV
    Available since
    Feb. 29, 2016
    Availability
    Academic Institutions and Nonprofits only
  4. mCherry-CRY2-5ptaseOCRL

    Plasmid
    #66836
    Purpose
    Expression of inositol 5-phosphatase domain of OCRL. Binds to CIBN upon blue light illumination.
    Depositor
    Has service
    50 µg Transfection-Ready DNA and 100 µg Transfection-Ready DNA
    Insert
    5ptaseOCRL (OCRL Human)
    Tags
    mCherry-CRY2
    Expression
    Mammalian
    Promoter
    CMV
    Available since
    June 22, 2015
    Availability
    Academic Institutions and Nonprofits only
    Cited by
  5. pBIR-GFP

    Plasmid
    #49807
    Purpose
    In vivo GFP based system to measure break induced replication (BIR) repair efficiency. expression of I-SceI generates a double strand break that when repaired by BIR mechanism will restore GFP.
    Depositor
    Has service
    50 µg Transfection-Ready DNA and 100 µg Transfection-Ready DNA
    Insert
    GFP
    Expression
    Mammalian
    Promoter
    beta-actin
    Available since
    Jan. 10, 2014
    Availability
    Academic Institutions and Nonprofits only
    Cited by
Showing: 5181 - 5200 of 79217 results