STAT2 KO (129) Macrophage Cell Line

A knockout signal transducer and activator of transcription 2 (STAT2) macrophage cell line isolated from bone marrow in 129 mice after immortalization with a retrovirus (J2) containing the myc and v-raf oncogenes.

All STAT molecules are phosphorylated by receptor associated kinases, that causes activation, dimerization by forming homo- or heterodimers and finally translocate to nucleus to work as transcription factors. STAT2 forms a complex with STAT1 and IFN regulatory factor family protein p48 (ISGF3G), in which this protein acts as a transactivator, but lacks the ability to bind DNA directly. 129 mice are widely used in the production of targeted mutations due to the availability of multiple embryonic stem cell lines derived from them. They also have a high incidence of spontaneous testicular teratomas.

From the laboratory of Howard A. Young, PhD, National Cancer Institute/NIH.

Catalog Number Product DataSheet Size AVAILABILITY Price Qty
ENH183-FP
STAT2 KO (129) Macrophage Cell Line
1 vial 4-6 weeks
Regular Price:$580.00
On Sale:

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Specifications

Product Type: Cell Line
Name: STAT2 KO (129)
Cell Type: Macrophage
Accession ID: P52630
Morphology: Adherent
Organism: Mouse
Source: Bone Marrow
Biosafety Level: BSL2
Growth Conditions: DMEM + 10% FBS + Glutamine
Cryopreservation: 90% FBS + 10% DMSO
Storage: Liquid Nitrogen
Shipped: Dry Ice

Provider
From the laboratory of Howard A. Young, PhD, National Cancer Institute/NIH.
Comments
The line is not producing any murine Type C retroviruses as it was derived with a replication defective packaging cell line.
References
  1. Blasi E, Radzioch D, Merletti L, Varesio L. Generation of macrophage cell line from fresh bone marrow cells with a myc/raf recombinant retrovirus. Cancer Biochem Biophys. 1989;10(4):303-317.
  2. Blasi E, Mathieson BJ, Varesio L, Cleveland JL, Borchert PA, Rapp UR. Selective immortalization of murine macrophages from fresh bone marrow by a raf/myc recombinant murine retrovirus. Nature. 1985;318(6047):667-670.
  3. Xiao C, Wang RH, Lahusen TJ, et al. Progression of chronic liver inflammation and fibrosis driven by activation of c-JUN signaling in Sirt6 mutant mice. J Biol Chem. 2012;287(50):41903-41913.

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