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On page 1 showing 1 ~ 20 out of 1,335 results
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  • RRID:CVCL_RM94

https://web.expasy.org/cellosaurus/CVCL_RM94

Organism: Homo sapiens (Human)
Disease:
Category: Induced pluripotent stem cell
Comments: Miscellaneous: Age/sex of donor from personal communication of Zambidis, Elias Thomas., Part of: NHBLI Progenitor Cell Biology Consortium (PCBC) collection.

Proper citation: WiCell Cat# cbips-6.13-pcbc, RRID:CVCL_RM94 Copy   


  • RRID:CVCL_YY10

https://web.expasy.org/cellosaurus/CVCL_YY10

Organism: Homo sapiens (Human)
Disease:
Category: Embryonic stem cell
Comments: Characteristics: Using a rAAV, the second B2M allele has been edited to express the signal sequence of HLA-G followed by a flexible (G4S)3 linker followed by B2M covalently linked at the C-terminus to a flexible (G4S)4 linker followed by HLA-E.

Proper citation: WiCell Cat# b2m-etrimer-elf1, RRID:CVCL_YY10 Copy   


https://web.expasy.org/cellosaurus/CVCL_A1HB

Organism: Homo sapiens (Human)
Disease:
Category: Embryonic stem cell
Comments: Characteristics: Using CRISPR/Cas9 a 2A-eGFP-PuroR cassette was integrated in front of the stop codon of one allele of EPHB4 (PubMed=28696312)., Characteristics: Using CRISPR/Cas9 a tdTomato-Neo cassette was integrated in front of the stop codon of one allele of EFNB2 (from parent cell line H1 EFNB2-tdTomato clone 14).

Proper citation: WiCell Cat# efnb2-tdtomato-ephb4-egfp, RRID:CVCL_A1HB Copy   


  • RRID:CVCL_UB73

https://web.expasy.org/cellosaurus/CVCL_UB73

Organism: Homo sapiens (Human)
Disease:
Category: Embryonic stem cell
Comments: Characteristics: Using TALEN a FLAG-citrine-P2A-PuroR construct was introduced at the C-terminal end of one allele of PAX6.

Proper citation: WiCell Cat# ai08e-pax6yfp, RRID:CVCL_UB73 Copy   


  • RRID:CVCL_UB78

https://web.expasy.org/cellosaurus/CVCL_UB78

Organism: Homo sapiens (Human)
Disease:
Category: Embryonic stem cell
Comments: Characteristics: Using TALEN a FLAG-citrine-P2A-PuroR construct was introduced at the C-terminal end of both alleles of HOPX.

Proper citation: WiCell Cat# ai13e-hopx-cit, RRID:CVCL_UB78 Copy   


  • RRID:CVCL_UB70

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_UB70

Organism: Homo sapiens (Human)
Disease:
Category: Embryonic stem cell
Comments: Characteristics: Using TALEN a FLAG-citrine-P2A-PuroR construct was introduced at the C-terminal end of the single copy DCX.

Proper citation: WiCell Cat# ai03e-dcxyfp, RRID:CVCL_UB70 Copy   


  • RRID:CVCL_UB75

https://web.expasy.org/cellosaurus/CVCL_UB75

Organism: Homo sapiens (Human)
Disease:
Category: Embryonic stem cell
Comments:

Proper citation: WiCell Cat# ai10e-kctd13b, RRID:CVCL_UB75 Copy   


  • RRID:CVCL_UB77

https://web.expasy.org/cellosaurus/CVCL_UB77

Organism: Homo sapiens (Human)
Disease:
Category: Embryonic stem cell
Comments: Characteristics: Using TALEN a FLAG-citrine-P2A-PuroR construct was introduced at the C-terminal end of one allele of HOPX.

Proper citation: WiCell Cat# ai12e-hopx-cit, RRID:CVCL_UB77 Copy   


  • RRID:CVCL_D1FD

https://web.expasy.org/cellosaurus/CVCL_D1FD

Organism: Homo sapiens (Human)
Disease: Down syndrome
Category: Induced pluripotent stem cell
Comments: Characteristics: This cell line has lot one copy of chromosome 21. Using CRISPR/Cas9 a IRES-TK-Neo-polyA site cassette was introduced in one allele of exon 3 of APP on chromosome 21 of the parent cell line. The parent cell line was cultured in the absence of G418 selection for three passages to allow chromosome loss to take place, and then were cultured in the presence of ganciclovir (GCV) to select a clone without the presence of the TK-neo construct (PubMed=23084023)., Population: Caucasian.

Proper citation: WiCell Cat# hipsc-di21-c2-4-4, RRID:CVCL_D1FD Copy   


  • RRID:CVCL_D1F9

https://web.expasy.org/cellosaurus/CVCL_D1F9

Organism: Homo sapiens (Human)
Disease: Down syndrome
Category: Induced pluripotent stem cell
Comments: Characteristics: Using CRISPR/Cas9 a IRES-TK-Neo-polyA site cassette was introduced in one allele of exon 3 of APP on chromosome 21 (PubMed=23084023)., Population: Caucasian.

Proper citation: WiCell Cat# hipsc-tri21-c2-4, RRID:CVCL_D1F9 Copy   


  • RRID:CVCL_D1FC

https://web.expasy.org/cellosaurus/CVCL_D1FC

Organism: Homo sapiens (Human)
Disease: Down syndrome
Category: Induced pluripotent stem cell
Comments: Characteristics: This cell line has lot one copy of chromosome 21. Using CRISPR/Cas9 a IRES-TK-Neo-polyA site cassette was introduced in one allele of exon 3 of APP on chromosome 21 of the parent cell line. The parent cell line was cultured in the absence of G418 selection for three passages to allow chromosome loss to take place, and then were cultured in the presence of ganciclovir (GCV) to select a clone without the presence of the TK-neo construct (PubMed=23084023)., Population: Caucasian.

Proper citation: WiCell Cat# hipsc-di21-c2-4-2, RRID:CVCL_D1FC Copy   


  • RRID:CVCL_JW69

https://web.expasy.org/cellosaurus/CVCL_JW69

Organism: Homo sapiens (Human)
Disease:
Category: Induced pluripotent stem cell
Comments: Population: Caucasian., From: University of Wisconsin; Madison; USA.

Proper citation: WiCell Cat# wisci004-a-3, RRID:CVCL_JW69 Copy   


  • RRID:CVCL_C1XM

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_C1XM

Organism: Homo sapiens (Human)
Disease:
Category: Induced pluripotent stem cell
Comments: Characteristics: Established from a patient that is mosaic for a trisomy 21, but this cell line does not contain the karyotypic abnormality., Population: Caucasian.

Proper citation: WiCell Cat# wc-24-02-ds-a, RRID:CVCL_C1XM Copy   


  • RRID:CVCL_C1XP

https://web.expasy.org/cellosaurus/CVCL_C1XP

Organism: Homo sapiens (Human)
Disease:
Category: Induced pluripotent stem cell
Comments: Characteristics: Established from a patient that is mosaic for a trisomy 21, but this cell line does not contain the karyotypic abnormality., Population: Caucasian.

Proper citation: WiCell Cat# wc-24-02-ds-c, RRID:CVCL_C1XP Copy   


  • RRID:CVCL_C1XQ

https://web.expasy.org/cellosaurus/CVCL_C1XQ

Organism: Homo sapiens (Human)
Disease: Down syndrome
Category: Induced pluripotent stem cell
Comments: Population: Caucasian.

Proper citation: WiCell Cat# wc-24-02-ds-m, RRID:CVCL_C1XQ Copy   


  • RRID:CVCL_U171

https://web.expasy.org/cellosaurus/CVCL_U171

Organism: Homo sapiens (Human)
Disease:
Category: Embryonic stem cell
Comments:

Proper citation: WiCell Cat# lt2e-h9caggfp, RRID:CVCL_U171 Copy   


  • RRID:CVCL_U161

https://web.expasy.org/cellosaurus/CVCL_U161

Organism: Homo sapiens (Human)
Disease:
Category: Embryonic stem cell
Comments:

Proper citation: WiCell Cat# h9-hnanog-pgz, RRID:CVCL_U161 Copy   


  • RRID:CVCL_U162

https://web.expasy.org/cellosaurus/CVCL_U162

Organism: Homo sapiens (Human)
Disease:
Category: Embryonic stem cell
Comments:

Proper citation: WiCell Cat# h9-hoct4-pgz, RRID:CVCL_U162 Copy   


  • RRID:CVCL_D092

https://web.expasy.org/cellosaurus/CVCL_D092

Organism: Homo sapiens (Human)
Disease:
Category: Embryonic stem cell
Comments: From: Monash University; Melbourne; Australia., From: ESI BIO - BioTime, Inc. (ES Cell International); Alameda; USA.

Proper citation: WiCell Cat# es01, RRID:CVCL_D092 Copy   


  • RRID:CVCL_D095

https://web.expasy.org/cellosaurus/CVCL_D095

Organism: Homo sapiens (Human)
Disease:
Category: Embryonic stem cell
Comments: From: ESI BIO - BioTime, Inc. (ES Cell International); Alameda; USA.

Proper citation: WiCell Cat# es05, RRID:CVCL_D095 Copy   



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