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Human IRF4 cDNA Clone in Bacterial Expression Vector (His-GST)

cDNA Clon Bacterial Expression Vector pPB-His-GST Kanamycin T7 Promoter His-GST Transient
Catalog No. ABIN4833651

Quick Overview for Human IRF4 cDNA Clone in Bacterial Expression Vector (His-GST) (ABIN4833651)

Gene

IRF4 (Interferon Regulatory Factor 4 (IRF4))

Fusion tag

His-GST

Application

Cloning (Clon)

Insert

cDNA

Vector

Bacterial Expression Vector

Vector Backbone

pPB-His-GST

Promoter

T7 Promoter

Bacterial Resistance

Kanamycin

Expression Type

Transient
  • Species

    Human

    Purpose

    Bacterial expression of Human IRF4 with His-GST

    Specificity

    5-NheI and 3-XhoI
    Fusion tag: Dual N-terminal tag, 6X Histidine followed by Glutathione-S-Transferase Protein which is cleavable with TEV (Size 27.9 kDa)

    Insert Length

    1356 bp

    Sequencing Primer

    GST Forward primer: 5'-CACGTTTGGTGGTGGCGAC3', T7 terminator primer: 5'-GCTAGTTATTGCTCAGCGG-3'
  • Application Notes

    The pPB vectors are low-medium copy number vectors in which the gene expression is driven by the strong T7 promoter.
    Below are some basic guidelines for using the pPB vectors for protein production:
    1. The pPB vectors are designed to be used with E. coli strains that are DE3 lysogens i.e. the host E. coli cell has a source of T7 RNA polymerase.
    2. Recombinant protein induction is usually done at OD600 of 0.6-1.2 using Isopropyl β-D-1-thiogalactopyranoside (IPTG) at a final concentration of 0.05 -1mM.
    3. The ideal concentration of IPTG must be determined empirically for each recombinant protein/cell-line. Similarly, the length of time and temperature for induction provide other variables that need to be optimized on a case-to-case basis.
    4. For toxic proteins, it is recommended to go for shorter induction time and also to try and suppress basal recombinant gene expression through (a) addition of glucose or use of pLysS plasmid. Please note that special cell-lines are also available in the market that cater to expression of toxic proteins.
    5. Once grown for the desired length of time, harvest cells by centrifugation and either freeze the cells at -80°C (as such or after re-suspending in the desired buffer) or proceed with the purification.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    10 mM Tris-HCI, 1 mM EDTA, pH 8.0

    Storage

    -20 °C

    Storage Comment

    1 year when stored at -20° C or lower in a non-frost free freezer.

    Expiry Date

    12 months
  • Target

    IRF4 (Interferon Regulatory Factor 4 (IRF4))

    Alternative Name

    IRF4
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