MCRIi031-A-1

Not yet reviewed by Australian Stem Cell Registry

468/SOX9-KO_het

Details

Tissue & Disease as reported

Disease as reported (Genomic Modifications)

Genetic Information

Genotype Locus
SOX9
Polymorphism
Heterozygous: unspecified_reference_SOX9:exon 1:partial deletion, exon 2:complete deletion, exon 3: partial deletion
Modifications
Gene Knock-out

Associated Publications

No available publications

Line Custodianship

Cell Line Maintainer

Ayers

Affiliated Institutions
  • Murdoch Children's Research Institute, Melbourne, Australia
View all cell lines from this group

Cell Line Producer

Murdoch Children's Research Institute

Affiliated Institutions
  • Murdoch Children's Research Institute, Melbourne, Australia

Derivation Details

Induced Pluripotent Cell Derivation Details

Source Cell Type: N/A

Source Cell Origin: N/A

Derivation Year:

Ethics

Ethics Number: Holding Entry-MCRIi031-A-1

Institution Human Research Ethics Council: Holding Entry

Approval Date: None

Modifications

Genomic Modifications

Heterozygous: unspecified_reference_SOX9:exon 1:partial deletion, exon 2:complete deletion, exon 3: partial deletion

Heterozygous partial deletion of SOX9 exons 1 and 3, and complete deletion of exon 2.

Cytoband: 17q24.3
Mutation Type: Gene Knock-out
Delivery Method: CRISPR/Cas9

Quality Assurance

Genomic Characterisation

Passage Number: 8

Karyotype: arr(1-22)x2,(XY)x1

Karyotype Method: Molecular karyotyping by SNP array

Summary: Molecular karyotyping by SNP array (Illumina Infinium GSA-24 v3.0, resolution 0.50Mb).

Microbiology and Virology Screening

No available data for this cell line.

Characterisation of Undifferentiated Cells

Marker Method
OCT3/4 Flow cytometry
SSEA-4 Flow cytometry
TRA-1-60 Flow cytometry
OCT3/4 Immunostaining
SOX2 Immunostaining

Scorecard Results

Undifferentiated Cells

No available data for this cell line.

Pluripotency

No available data for this cell line.

Pluripotency Characterisation

Endoderm

In vitro spontaneous differentiation

Assessed by: Immunostaining

Markers: SOX17

Mesoderm

In vitro spontaneous differentiation

Assessed by: Immunostaining

Markers: SMA

Ectoderm

In vitro spontaneous differentiation

Assessed by: Immunostaining

Markers: MAP2

Growth Characteristics

Culture Medium and Growth Conditions

CO2 concentration: 5%

O2 concentration: 20%

Medium Items:

  • Base Medium: Essential 8 Medium - Thermo Fisher Scientific Inc.
  • Base Coat: Matrigel - Corning

Passage Method: Enzyme-free cell dissociation