Astrocyte LKB1 Knock Out Cell Line (ALKO)

Immortalized mouse astrocyte cell line (ALKO) with a stable knock out of liver kinase B1 (LKB1). Useful as a model for gliomas or for stem cell research.

Highlights:

  • Exhibit anchorage independent growth with doubling time of less than 24 hr
  • Express reduced levels of astrocyte marker GFAP (Glial fibrillary acidic protein)
  • Express stem cell markers including Sox2 and Oct4
  • Useful as a model for gliomas or for stem cell research

Liver kinase B1 (LKB1, also referred to as Serine/threonine-protein kinase STK11, Renal carcinoma antigen NY-REN-19) is a tumor suppressor serine/threonine-protein kinase that controls the activity of a large number of protein kinases including AMP-activated protein kinase (AMPK) family members, thereby playing a role in various processes such as cell metabolism, cell polarity, and apoptosis.

From the laboratory of Douglas L. Feinstein, PhD, University of Illinois at Chicago.

The Investigator's Annexe Part of The Investigator's Annexe program.

Catalog Number Product Size AVAILABILITY Price Qty
EB9001
Astrocyte LKB1 Knock Out Cell Line (ALKO), 1 vial
1 vial In stock
Price: $799.00

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Specifications
Name: ALKO (astrocyte LKB1 knock out)
Cell Type: Transformed mouse astrocyte
Organism: Mouse
Accession ID: CVCL_5I28
Morphology: Fibroblast
Biosafety Level: BSL1
Subculturing: Standard trypsinization followed by 1:10 dilution
Growth Conditions: DMEM 10% FCS A/A
Cryopreservation: 10% DMSO in FBS
Source: Brain
Storage: Liquid nitrogen
Shipped: Dry ice
Provider
From the laboratory of Douglas L. Feinstein, PhD, University of Illinois at Chicago.
Comments

Mouse ALKO cells (astrocyte LKB1 knock out) were prepared by treating astrocytes harboring a floxed version of the LKB1 gene with Adeno Associated Virus expressing the bacterial Cre-recombinase. After several passages, the resulting cells show anchorage independent growth, have a doubling time of less than 24 hr, lose expression of the astrocyte marker GFAP (Glial fibrillary acidic protein), and gain expression of stem cell markers including Sox2 and Oct4.

References

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