GZNLi001-A-1

iCas9-NKX2-1 EGFP

The cell line is not validated yet.

General

iPSC Line

hPSCreg name GZNLi001-A-1
Cite as:
GZNLi001-A-1
Alternative name(s)
iCas9-NKX2-1 EGFP
iPSC line type Human induced pluripotent stem cell (hiPSC)
Similar iPSC lines No similar lines found.
Last update 18th June 2026
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Provider

Generator Guangzhou Laboratory (GZNL)
Owner Guangzhou Laboratory (GZNL)

External iPSC Databases

BioSamples SAMEA122892933

General iPSC Information

* Is the cell line readily obtainable for third parties?
Yes
Research use: allowed
Clinical use: not allowed
Commercial use: not allowed
Subclone of

iPSC Genetic Modification

Genetic modifications not related to a disease
NKX2-1 (target)
Gene knock-in
14q13.3
GFP
14q13.3
EGFP was knocked in via CRISPR/Cas9-mediated homology-directed repair (HDR). Correct integration was confirmed by Sanger sequencing, and immunofluorescence validated co-expression with NKX2-1 in differentiated cells.
CRISPR-associated (CRISPR/Cas) System
AAVS1 (target)
Gene knock-in
19p13.3
Cas9
19p13.3
Western Blot and gel electrophoresis further validated the expression of the Cas9 protein in the modified iPSCs.
CRISPR-associated (CRISPR/Cas) System

Donor Information

General Donor Information

Sex female
Ethnicity Ethnicity asian

Phenotype and Disease related information (Donor)

Diseases No disease was diagnosed.

Other Genotyping (Donor)

Is there genome-wide genotyping or functional data available?
No

External Databases (Donor)

BioSamples SAMEA122891895

Ethics

Also have a look at the ethics information for the parental line GZNLi001-A .
Is there an MTA available for the cell line? No
For generation of the cell line, who was the supplier of any recombined DNA vectors or commercial kits used? Addgene
Are you aware of any constraints on the use or distribution of the cell line from the owner or any parties identified in the query above? No

iPSC Derivation

General

The source cell information can be found in the parental cell line GZNLi001-A.

Reprogramming method

Vector type Integrating
Vector Virus (Retrovirus)
Genes
Is the used vector excisable?
No
Absence of reprogramming vector(s)?
No
Reprogramming vectors silenced?
Yes
Methods used
RT-PCR

Vector free reprogramming

Other

Selection criteria for clones Clones were selected based on compact, dome-shaped morphology with a high nuclear-to-cytoplasmic ratio, and confirmed by positive alkaline phosphatase (AP) staining.
Derived under xeno-free conditions
No
Derived under GMP?
No
Available as clinical grade?
No

iPSC Culture Conditions

Surface coating Matrigel/Geltrex
Feeder cells
No
O2 Concentration 5 %
CO2 Concentration 5 %
Medium mTeSR™ 1
Has Rock inhibitor (Y27632) been used at passage previously with this iPSC line?
Yes
Has Rock inhibitor (Y27632) been used at cryo previously with this iPSC line?
No
Has Rock inhibitor (Y27632) been used at thaw previously with this iPSC line?
Yes

iPSC Characterisation

Analysis of undifferentiated iPSCs
Marker Expressed Immunostaining RT-PCR Flow Cytometry Enzymatic Assay Expression Profiles
POU5F1 (OCT-4)
Yes
NANOG
Yes
SOX2
Yes
Morphology pictures
Self-renewal
Positive
Endoderm
Positive
Mesoderm
Positive
Ectoderm score
Positive
Data analysis report
Differentiation Potency
Endoderm
Ont Id: UBERON_0000925
In vitro directed differentiation
Marker Expressed
FOXA2
Yes
SOX17
Yes
Protocol or reference
Mesoderm
Ont Id: UBERON_0000926
In vitro directed differentiation
Marker Expressed
HAND1
Yes
TBXT
Yes
Protocol or reference
Ectoderm
Ont Id: UBERON_0000924
In vitro directed differentiation
Marker Expressed
PAX6
Yes
OTX2
Yes
Protocol or reference

Microbiology / Virus Screening

Genotyping

Karyotyping (iPSC Line)

Has the iPSC line karyotype been analysed?
Yes
46,XX
Passage number: 10
Karyotyping method: G-Banding

Other Genotyping (iPSC Line)