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Addgene

pBZ-attBtxnl4b
(Plasmid #18667)

Ordering

This material is available to academics and nonprofits only.
Item Catalog # Description Quantity Price (USD)
Plasmid 18667 Standard format: Plasmid sent in bacteria as agar stab 1 $85

Backbone

  • Vector backbone
    pBZ
  • Backbone size w/o insert (bp) 2930
  • Total vector size (bp) 3495
  • Modifications to backbone
    pBZ is a derivative of pBlueScript II SK with a modified multiple cloning site (MCS).
  • Vector type
    Bacterial Expression

Growth in Bacteria

  • Bacterial Resistance(s)
    Ampicillin, 100 μg/mL
  • Growth Temperature
    37°C
  • Growth Strain(s)
    DH5alpha
  • Copy number
    Unknown

Gene/Insert

  • Gene/Insert name
    thioredoxin-like 4B
  • Alt name
    TXNL4B
  • Alt name
    human Dim2
  • Species
    H. sapiens (human)
  • Insert Size (bp)
    565
  • Entrez Gene
    TXNL4B (a.k.a. DLP, Dim2, FLJ20511)
  • Promoter T3

Cloning Information

  • Cloning method Restriction Enzyme
  • 5′ cloning site NotI (not destroyed)
  • 3′ cloning site BamHI (not destroyed)
  • 5′ sequencing primer T3
  • 3′ sequencing primer T7
  • (Common Sequencing Primers)

Terms and Licenses

  • Academic/Nonprofit Terms
  • Industry Terms
    • Not Available to Industry
Trademarks:
  • Zeocin® is an InvivoGen trademark.

Depositor Comments

attB cassette flanking coding region of TXNL4B (dim2) can be released by digestion with NotI and BamHI

How to cite this plasmid ( Back to top)

These plasmids were created by your colleagues. Please acknowledge the Principal Investigator, cite the article in which the plasmids were described, and include Addgene in the Materials and Methods of your future publications.

  • For your Materials & Methods section:

    pBZ-attBtxnl4b was a gift from Yu-Zhu Zhang (Addgene plasmid # 18667 ; http://n2t.net/addgene:18667 ; RRID:Addgene_18667)
  • For your References section:

    An in vitro recombination method to convert restriction- and ligation-independent expression vectors. Guo F, Chiang MY, Wang Y, Zhang YZ. Biotechnol J. 2008 Mar . 3(3):370-7. 10.1002/biot.200700170 PubMed 18064608