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On page 9 showing 161 ~ 180 out of 1,144 results
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  • RRID:CVCL_M266

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_M266

Organism: Homo sapiens (Human)
Disease:
Category: Telomerase immortalized cell line
Comments: Characteristics: Transduced with a retroviral vector SSR#197 (MoMLV/LTR-LoxP-hTERT-IRES-EGFP-LoxP-MoMLV/LTR) expressing hTERT and eGFP flanked by a pair of loxP sites., Characteristics: Because it has been transduced by a construct containing LoxP sites, transfection with the Cre recombinase eliminates the SV40 T gene thus reverting the cells to a non-immortal phenotype., Population: Japanese., Group: Patented cell line.

Proper citation: JCRB Cat# JCRB1554, RRID:CVCL_M266 Copy   


  • RRID:CVCL_Z064

https://web.expasy.org/cellosaurus/CVCL_Z064

Organism: Homo sapiens (Human)
Disease:
Category: Telomerase immortalized cell line
Comments: Characteristics: When cells are exposed to inflammatory cytokines such as TNFalpha, activation of the NF-kappaB signaling pathway occurs resulting in increased luciferase activity (ATCC=CRL-4049)., Characteristics: The NanoLuc reporter gene is under the control of multiple copies of the NF-kappaB response element (ATCC=CRL-4049).

Proper citation: ATCC Cat# CRL-4049, RRID:CVCL_Z064 Copy   


  • RRID:CVCL_ZZ92

https://web.expasy.org/cellosaurus/CVCL_ZZ92

Organism: Homo sapiens (Human)
Disease:
Category: Telomerase immortalized cell line
Comments:

Proper citation: ECACC Cat# 20012016, RRID:CVCL_ZZ92 Copy   


https://web.expasy.org/cellosaurus/CVCL_B4N4

Organism: Homo sapiens (Human)
Disease: Werner syndrome
Category: Telomerase immortalized cell line
Comments: Population: Caucasian; Spanish.

Proper citation: RRID:CVCL_B4N4 Copy   


  • RRID:CVCL_K051

https://web.expasy.org/cellosaurus/CVCL_K051

Organism: Homo sapiens (Human)
Disease: BRCA1 syndrome
Category: Telomerase immortalized cell line
Comments:

Proper citation: RRID:CVCL_K051 Copy   


  • RRID:CVCL_6880

https://web.expasy.org/cellosaurus/CVCL_6880

Organism: Homo sapiens (Human)
Disease:
Category: Telomerase immortalized cell line
Comments:

Proper citation: RRID:CVCL_6880 Copy   


  • RRID:CVCL_DP18

https://web.expasy.org/cellosaurus/CVCL_DP18

Organism: Homo sapiens (Human)
Disease:
Category: Telomerase immortalized cell line
Comments:

Proper citation: RRID:CVCL_DP18 Copy   


  • RRID:CVCL_DP16

https://web.expasy.org/cellosaurus/CVCL_DP16

Organism: Homo sapiens (Human)
Disease:
Category: Telomerase immortalized cell line
Comments:

Proper citation: RRID:CVCL_DP16 Copy   


  • RRID:CVCL_4M95

https://web.expasy.org/cellosaurus/CVCL_4M95

Organism: Homo sapiens (Human)
Disease: Barrett esophagus
Category: Telomerase immortalized cell line
Comments:

Proper citation: RRID:CVCL_4M95 Copy   


  • RRID:CVCL_A1TM

https://web.expasy.org/cellosaurus/CVCL_A1TM

Organism: Homo sapiens (Human)
Disease:
Category: Telomerase immortalized cell line
Comments: Population: Chinese.

Proper citation: RRID:CVCL_A1TM Copy   


  • RRID:CVCL_A5XS

https://web.expasy.org/cellosaurus/CVCL_A5XS

Organism: Homo sapiens (Human)
Disease: Follicular ameloblastoma
Category: Telomerase immortalized cell line
Comments: Population: Japanese.

Proper citation: RRID:CVCL_A5XS Copy   


  • RRID:CVCL_A2GP

https://web.expasy.org/cellosaurus/CVCL_A2GP

Organism: Homo sapiens (Human)
Disease: Polycystic ovary syndrome
Category: Telomerase immortalized cell line
Comments: Miscellaneous: Doubling time and info on hygromycin vector from personal communication of Nasimian, Ahmad., Population: Iranian.

Proper citation: RRID:CVCL_A2GP Copy   


  • RRID:CVCL_3473

Discontinued

https://web.expasy.org/cellosaurus/CVCL_3473

Organism: Homo sapiens (Human)
Disease: Hereditary glomangioma
Category: Telomerase immortalized cell line
Comments:

Proper citation: RRID:CVCL_3473 Copy   


  • RRID:CVCL_ZV77

https://web.expasy.org/cellosaurus/CVCL_ZV77

Organism: Homo sapiens (Human)
Disease: Seckel syndrome
Category: Telomerase immortalized cell line
Comments: Population: Pakistani.

Proper citation: RRID:CVCL_ZV77 Copy   


  • RRID:CVCL_VL08

https://web.expasy.org/cellosaurus/CVCL_VL08

Organism: Homo sapiens (Human)
Disease: Nijmegen breakage syndrome-like disorder
Category: Telomerase immortalized cell line
Comments:

Proper citation: RRID:CVCL_VL08 Copy   


  • RRID:CVCL_6F48

https://web.expasy.org/cellosaurus/CVCL_6F48

Organism: Muntiacus muntjak (Barking deer)
Disease:
Category: Telomerase immortalized cell line
Comments:

Proper citation: RRID:CVCL_6F48 Copy   


  • RRID:CVCL_D254

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_D254

Organism: Homo sapiens (Human)
Disease: Fanconi anemia, complementation group G
Category: Telomerase immortalized cell line
Comments: Population: Japanese.

Proper citation: RRID:CVCL_D254 Copy   


  • RRID:CVCL_D253

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_D253

Organism: Homo sapiens (Human)
Disease: Fanconi anemia, complementation group A
Category: Telomerase immortalized cell line
Comments: Population: Japanese.

Proper citation: RRID:CVCL_D253 Copy   


  • RRID:CVCL_2897

Discontinued

https://web.expasy.org/cellosaurus/CVCL_2897

Organism: Homo sapiens (Human)
Disease: Fanconi anemia, complementation group G
Category: Telomerase immortalized cell line
Comments: Population: Japanese.

Proper citation: RRID:CVCL_2897 Copy   


  • RRID:CVCL_ZT72

https://web.expasy.org/cellosaurus/CVCL_ZT72

Organism: Homo sapiens (Human)
Disease: Ataxia-oculomotor apraxia type 1
Category: Telomerase immortalized cell line
Comments:

Proper citation: RRID:CVCL_ZT72 Copy   



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