Searching the RRID Resource Information Network
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Cellosaurus is database indexing available cell lines from various collections: American Type Culture Collection (ATCC), Bioresource Collection and Research Center, Taiwan (BCRC), Banco de Células do Rio de Janeiro (BCRJ), CellBank Australia (CBA), Collection of Cell Lines in Veterinary Medicine (CCLV), Cell Lines Service (CLS), Coriell, Drosophila Genomics Resource Center (DGRC), Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH (DSMZ), European Bank for induced pluripotent Stem Cells (EBiSC), European Collection of Authenticated Cell Cultures (ECACC), Interlab Cell Line Collection (ICLC), Institute for Fermentation Osaka (IFO), Istituto Zooprofilattico Sperimentale della Lombardia e dell'Emilia Romagna (IZSLER) biobank, Japanese Collection of Research Bioresources (JCRB) Cell Bank, Kunming Cell Bank of Type Culture Collection (KCB), Korean Cell Line Bank (KCLB), Millipore, National Cell Bank of Iran (NCBI_Iran), National Cancer Institute - Developmental Therapeutics Program (NCI-DTP), NINDS Human Cell and Data Repository (NHCDR), NIH AIDS Reagent Program (NIH-ARP), NISES, RIKEN Bioresource Center Cell Bank (RCB), Royan Stem Cell Bank (RSCB), Tick Cell Biobank (TCB), Tohoku University cell line catalog (TKG), and Ximbio.
| Name | Proper Citation | Organism | Disease |
Comments |
Defining Citation | Category | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
DD1679 Resource Report Resource Website |
ECACC Cat# 93122102, RRID:CVCL_9H02 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 93122102 | ECACC:93122102, Wikidata:Q54829915 |
CVCL_9H02 | 2026-08-15 04:26:41 | 0 | |||||
|
DD1719 Resource Report Resource Website |
ECACC Cat# 94012020, RRID:CVCL_9H19 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 94012020 | ECACC:94012020, Wikidata:Q54829935 |
CVCL_9H19 | 2026-08-15 04:26:42 | 0 | |||||
|
DD1655 Resource Report Resource Website |
ECACC Cat# 93121403, RRID:CVCL_9G91 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 93121403 | ECACC:93121403, Wikidata:Q54829904 |
CVCL_9G91 | 2026-08-15 04:26:43 | 0 | |||||
|
DD1716 Resource Report Resource Website |
ECACC Cat# 94011707, RRID:CVCL_9H17 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 94011707 | ECACC:94011707, Wikidata:Q54829933 |
CVCL_9H17 | 2026-08-15 04:26:43 | 0 | |||||
|
DD1706 Resource Report Resource Website |
ECACC Cat# 94011319, RRID:CVCL_9H10 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 94011319 | ECACC:94011319, Wikidata:Q54829926 |
CVCL_9H10 | 2026-08-15 04:26:42 | 0 | |||||
|
DD1660 Resource Report Resource Website |
ECACC Cat# 93121504, RRID:CVCL_9G94 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 93121504 | ECACC:93121504, Wikidata:Q54829907 |
CVCL_9G94 | 2026-08-15 04:26:43 | 0 | |||||
|
DD1708 Resource Report Resource Website |
ECACC Cat# 94011321, RRID:CVCL_9H12 | Homo sapiens (Human) | Aniridia | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 94011321 | ECACC:94011321, Wikidata:Q54829928 |
CVCL_9H12 | 2026-08-15 04:26:42 | 0 | ||||
|
DD1689 Resource Report Resource Website |
ECACC Cat# 93122304, RRID:CVCL_9H04 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 93122304 | ECACC:93122304, Wikidata:Q54829920 |
CVCL_9H04 | 2026-08-15 04:26:41 | 0 | |||||
|
DD1666 Resource Report Resource Website |
ECACC Cat# 93121705, RRID:CVCL_9G97 | Homo sapiens (Human) | Karyotypic information: 46,XX,t(1;15)(q14.2;q26.3)pat (ECACC=93121705)., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 93121705 | ECACC:93121705, Wikidata:Q54829910 |
CVCL_9G97 | 2026-08-15 04:26:43 | 0 | |||||
|
DD1724 Resource Report Resource Website |
ECACC Cat# 94012506, RRID:CVCL_9H24 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 94012506 | ECACC:94012506, Wikidata:Q54829940 |
CVCL_9H24 | 2026-08-15 04:26:42 | 0 | |||||
|
DD1720 Resource Report Resource Website |
ECACC Cat# 94012132, RRID:CVCL_9H20 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 94012132 | ECACC:94012132, Wikidata:Q54829936 |
CVCL_9H20 | 2026-08-15 04:26:44 | 0 | |||||
|
DD1668 Resource Report Resource Website |
ECACC Cat# 93121707, RRID:CVCL_9G98 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 93121707 | ECACC:93121707, Wikidata:Q54829911 |
CVCL_9G98 | 2026-08-15 04:26:41 | 0 | |||||
|
DD1641 Resource Report Resource Website |
ECACC Cat# 93120316, RRID:CVCL_9G83 | Homo sapiens (Human) | 22q11.2 deletion syndrome | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 93120316 | ECACC:93120316, Wikidata:Q54829896 |
CVCL_9G83 | 2026-08-15 04:26:41 | 0 | ||||
|
DD1714 Resource Report Resource Website |
ECACC Cat# 94011705, RRID:CVCL_9H15 | Homo sapiens (Human) | Fragile X syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 94011705 | ECACC:94011705, Wikidata:Q54829931 |
CVCL_9H15 | 2026-08-15 04:26:42 | 0 | ||||
|
DD1649 Resource Report Resource Website |
ECACC Cat# 931207125, RRID:CVCL_9G89 | Homo sapiens (Human) | 22q11.2 deletion syndrome | Karyotypic information: 46,XX,del(22) (ECACC=931207125)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 931207125 | ECACC:931207125, Wikidata:Q54829902 |
CVCL_9G89 | 2026-08-15 04:26:41 | 0 | ||||
|
DD1693 Resource Report Resource Website |
ECACC Cat# 94010501, RRID:CVCL_9H06 | Homo sapiens (Human) | Turner syndrome | Karyotypic information: 45,X0 (ECACC=94010501)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 94010501 | ECACC:94010501, Wikidata:Q54829922 |
CVCL_9H06 | 2026-08-15 04:26:41 | 0 | ||||
|
DD1715 Resource Report Resource Website |
ECACC Cat# 94011706, RRID:CVCL_9H16 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 94011706 | ECACC:94011706, Wikidata:Q54829932 |
CVCL_9H16 | 2026-08-15 04:26:42 | 0 | |||||
|
DD1725 Resource Report Resource Website |
ECACC Cat# 94012507, RRID:CVCL_9H25 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 94012507 | ECACC:94012507, Wikidata:Q54829941 |
CVCL_9H25 | 2026-08-15 04:26:42 | 0 | |||||
|
DD1722 Resource Report Resource Website |
ECACC Cat# 94012134, RRID:CVCL_9H22 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 94012134 | ECACC:94012134, Wikidata:Q54829938 |
CVCL_9H22 | 2026-08-15 04:26:42 | 0 | |||||
|
DD3073 Resource Report Resource Website |
ECACC Cat# 98031003, RRID:CVCL_9M09 | Homo sapiens (Human) | Karyotypic information: 46,XY,t(1;8)(p32;q13); de novo (ECACC=98031003)., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 98031003 | ECACC:98031003, Wikidata:Q54830544 |
CVCL_9M09 | 2026-08-15 04:27:00 | 0 |
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