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On page 348 showing 6941 ~ 6960 out of 6,967 results
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  • RRID:CVCL_3643

Partially Contaminated Discontinued Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_3643

Organism: Homo sapiens (Human)
Disease: Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
Category: Finite cell line
Comments: Senescence: Senesces at ~40 PDL (ATCC=CCL-124)., Population: Caucasian., Problematic cell line: Partially contaminated. Some stocks were contaminated by pig LLC-PK1 (PubMed=14505435; PubMed=20143388)..

Proper citation: ECACC Cat# 90112605, RRID:CVCL_3643 Copy   


  • RRID:CVCL_E461

https://web.expasy.org/cellosaurus/CVCL_E461

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian; Danish., Part of: 12th International Histocompatibility Workshop (12IHW) cell line panel.

Proper citation: ECACC Cat# 94071428, RRID:CVCL_E461 Copy   


  • RRID:CVCL_8B48

Discontinued

https://web.expasy.org/cellosaurus/CVCL_8B48

Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 90070301, RRID:CVCL_8B48 Copy   


  • RRID:CVCL_8B53

Discontinued

https://web.expasy.org/cellosaurus/CVCL_8B53

Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 90091901, RRID:CVCL_8B53 Copy   


  • RRID:CVCL_K159

https://web.expasy.org/cellosaurus/CVCL_K159

Organism: Rattus norvegicus (Rat)
Category: Hybridoma

Proper citation: ECACC Cat# 85102271, RRID:CVCL_K159 Copy   


  • RRID:CVCL_8B55

Discontinued

https://web.expasy.org/cellosaurus/CVCL_8B55

Organism: Homo sapiens (Human)
Disease: Familial adenomatous polyposis
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 91010404, RRID:CVCL_8B55 Copy   


  • RRID:CVCL_8B56

Discontinued

https://web.expasy.org/cellosaurus/CVCL_8B56

Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 91072504, RRID:CVCL_8B56 Copy   


  • RRID:CVCL_8B60

Discontinued

https://web.expasy.org/cellosaurus/CVCL_8B60

Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 91091602, RRID:CVCL_8B60 Copy   


  • RRID:CVCL_8B59

Discontinued

https://web.expasy.org/cellosaurus/CVCL_8B59

Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 91082128, RRID:CVCL_8B59 Copy   


  • RRID:CVCL_8B58

Discontinued

https://web.expasy.org/cellosaurus/CVCL_8B58

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 91081204, RRID:CVCL_8B58 Copy   


  • RRID:CVCL_8B61

Discontinued

https://web.expasy.org/cellosaurus/CVCL_8B61

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 91092529, RRID:CVCL_8B61 Copy   


  • RRID:CVCL_8B64

Discontinued

https://web.expasy.org/cellosaurus/CVCL_8B64

Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 91092608, RRID:CVCL_8B64 Copy   


  • RRID:CVCL_8B57

Discontinued

https://web.expasy.org/cellosaurus/CVCL_8B57

Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 91081203, RRID:CVCL_8B57 Copy   


  • RRID:CVCL_8B62

Discontinued

https://web.expasy.org/cellosaurus/CVCL_8B62

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 91092530, RRID:CVCL_8B62 Copy   


  • RRID:CVCL_8B67

Discontinued

https://web.expasy.org/cellosaurus/CVCL_8B67

Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 91102207, RRID:CVCL_8B67 Copy   


  • RRID:CVCL_8B65

Discontinued

https://web.expasy.org/cellosaurus/CVCL_8B65

Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 91100410, RRID:CVCL_8B65 Copy   


  • RRID:CVCL_8B77

Discontinued

https://web.expasy.org/cellosaurus/CVCL_8B77

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 94101410, RRID:CVCL_8B77 Copy   


  • RRID:CVCL_8B74

Discontinued

https://web.expasy.org/cellosaurus/CVCL_8B74

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 94101407, RRID:CVCL_8B74 Copy   


  • RRID:CVCL_8B75

Discontinued

https://web.expasy.org/cellosaurus/CVCL_8B75

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 94101408, RRID:CVCL_8B75 Copy   


  • RRID:CVCL_GR82

Discontinued

https://web.expasy.org/cellosaurus/CVCL_GR82

Organism: Homo sapiens (Human)
Disease: Fanconi anemia, complementation group J
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 04101820, RRID:CVCL_GR82 Copy   



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