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6,967 Results - per page

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Name Proper Citation Organism Disease Comments Defining Citation Category Sex Synonyms Vendor Catalog Number Cross References Hierarchy Originate from Same Individual ID Record Last Update Mentions Count
PFIZi012-A
 
Resource Report
Resource Website
ECACC Cat# 66540228, RRID:CVCL_VE73 Homo sapiens (Human) Chromosome 16p11.2 deletion syndrome From: Pfizer, Inc.; New York; USA. Induced pluripotent stem cell Sex unspecified FB66c17, RCi198 ECACC 66540228 BioSamples:SAMEA4097192,
EBiSC:PFIZi012-A,
ECACC:66540228,
hPSCreg:PFIZi012-A,
Wikidata:Q54947266
CVCL_VE73 2026-08-29 04:56:31 0
PF97387
 
Resource Report
Resource Website
ECACC Cat# 95042722, RRID:CVCL_E805 Homo sapiens (Human) Population: Caucasian; French., Part of: 10th International Histocompatibility Workshop (10IHW) cell line panel. PMID:8813743
PMID:28360230
PMID:29171935
PMID:30844424
Transformed cell line Male PF 97387 ECACC 95042722 CLDB:cl7226,
dbMHC:49000,
ECACC:95042722,
ICLC:HTL14004,
IHW:IHW09027,
IPD-IMGT/HLA:11644,
Wikidata:Q54947246
CVCL_E805 2026-08-29 04:56:30 0
PFIZi010-B
 
Resource Report
Resource Website
ECACC Cat# 66540171, RRID:CVCL_VE70 Homo sapiens (Human) Chromosome 16p11.2 deletion syndrome From: Pfizer, Inc.; New York; USA. Induced pluripotent stem cell Female FB65c16 ECACC 66540171 BioSamples:SAMEA4091043,
EBiSC:PFIZi010-B,
ECACC:66540171,
hPSCreg:PFIZi010-B,
Wikidata:Q54947263
CVCL_VE70 2026-08-29 04:56:31 0
PFIZi011-A
 
Resource Report
Resource Website
ECACC Cat# 66540227, RRID:CVCL_VE72 Homo sapiens (Human) Chromosome 16p11.2 deletion syndrome From: Pfizer, Inc.; New York; USA. Induced pluripotent stem cell Male FB67c2, RCi199 ECACC 66540227 BioSamples:SAMEA4097152,
EBiSC:PFIZi011-A,
ECACC:66540227,
hPSCreg:PFIZi011-A,
Wikidata:Q54947265
CVCL_VE72 2026-08-29 04:56:31 0
Pl 1Ut
 
Resource Report
Resource Website
Discontinued
ECACC Cat# 90111909, RRID:CVCL_3771 Procyon lotor (Raccoon) Part of: Naval Biosciences Laboratory (NBL) collection (transferred to ATCC in 1982). Finite cell line Female Pl 1Ut (NBL-9), Pl 1 Ut (NBL-9), NBL-9, Pl.1 Ut, Pl 1 UT, Pl 1 Ut, Procyon lotor 1 Uterus ECACC 90111909 CLO:CLO_0008287,
CLO:CLO_0008443,
CLDB:cl3910,
ATCC:CCL-74,
ATCC:CRL-6596,
ECACC:90111909,
Wikidata:Q54947483
CVCL_3771 2026-08-29 04:56:38 0
PM0001
 
Resource Report
Resource Website
ECACC Cat# 01020501, RRID:CVCL_8Y28 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Sex unspecified ECACC 01020501 ECACC:01020501,
Wikidata:Q54947606
CVCL_8Y28 2026-08-29 04:56:42 0
PNMR OE
 
Resource Report
Resource Website
ECACC Cat# 01080925, RRID:CVCL_U059 Mus musculus (Mouse) PMID:11461669 Hybridoma OE ECACC 01080925 ECACC:01080925,
Wikidata:Q54947675
cvcl_2199 CVCL_U059 2026-08-29 04:56:34 0
PNV35B
 
Resource Report
Resource Website
ECACC Cat# 01080924, RRID:CVCL_U068 Mus musculus (Mouse) Caution: Stated to be generated by fusion with Ag876 myeloma cells (PubMed=10656666), but AG876 is a Burkitt lymphoma cell line. PMID:10656666 Hybridoma V35B ECACC 01080924 ECACC:01080924,
Wikidata:Q54947689
CVCL_U068 2026-08-29 04:56:44 0
PMH161
 
Resource Report
Resource Website
ECACC Cat# 94062301, RRID:CVCL_E812 Homo sapiens (Human) Population: Korean., Part of: 12th International Histocompatibility Workshop (12IHW) cell line panel. PMID:30844424 Transformed cell line Male ECACC 94062301 dbMHC:49006,
ECACC:94062301,
IHW:IHW09351,
IPD-IMGT/HLA:11261,
Wikidata:Q54947641
CVCL_E812 2026-08-29 04:56:34 0
PNT1A serum free
 
Resource Report
Resource Website
ECACC Cat# 07052901, RRID:CVCL_JX33 Homo sapiens (Human) Group: Serum/protein free medium cell line. Transformed cell line Male PNT1A (SERUM FREE) ECACC 07052901 ECACC:07052901,
Wikidata:Q54947680
cvcl_2163 CVCL_JX33 2026-08-29 04:56:35 0
PNT1A
 
Resource Report
Resource Website
1+ mentions
ECACC Cat# 95012614, RRID:CVCL_2163 Homo sapiens (Human) PMID:7558421
PMID:11416159
PMID:11694337
PMID:20215515
PMID:21556542
Transformed cell line Male PNT1a, PNT-1A, PNT1-a, PNT1/A ECACC 95012614 BTO:BTO_0003068,
CLO:CLO_0008475,
CLDB:cl3926,
ChEMBL-Cells:CHEMBL4513117,
ChEMBL-Targets:CHEMBL4513131,
ECACC:95012614,
GEO:GSM827411,
GEO:GSM1374835,
PubChem_Cell_line:CVCL_2163,
Wikidata:Q54947679
cvcl_4804 CVCL_2163 2026-08-29 04:56:44 6
PQXB1/2
 
Resource Report
Resource Website
Discontinued
ECACC Cat# 89050503, RRID:CVCL_A6JY Mus musculus (Mouse) PMID:7766007
PMID:8267405
PMID:18623591
Hybridoma PQXB 1/2 ECACC 89050503 ECACC:89050503,
Wikidata:Q107116674
cvcl_4032 CVCL_A6JY 2026-08-29 04:56:37 0
SOL,CA
 
Resource Report
Resource Website
ECACC Cat# 94082252, RRID:CVCL_E832 Homo sapiens (Human) Part of: 4th Asia-Oceania Histocompatibility Workshop (4AOHW) cell line panel. PMID:8307784
PMID:30844424
Transformed cell line Sex unspecified SOL, CA ECACC 94082252 dbMHC:49023,
ECACC:94082252,
IHW:IHW09152,
IPD-IMGT/HLA:11695,
Wikidata:Q54955373
CVCL_E832 2026-08-29 04:59:54 0
SP08.1
 
Resource Report
Resource Website
ECACC Cat# 66540067, RRID:CVCL_V202 Homo sapiens (Human) Parkinson disease From: Institut de Bioenginyeria de Catalunya (IBEC); Barcelona; Spain., Part of: Spanish Stem Cell Bank (Banco Nacional de Lineas Celulares) collection. PMID:22407749 Induced pluripotent stem cell Female SP08#1, ESi002-A ECACC 66540067 BioSamples:SAMEA3303008,
EBiSC:ESi002-A,
ECACC:66540067,
hPSCreg:ESi002-A,
SKIP:SKIP000942,
SKIP:SKIP002420,
Wikidata:Q54955406
CVCL_V202 2026-08-29 04:59:51 0
SP3033
 
Resource Report
Resource Website
ECACC Cat# 15103006, RRID:CVCL_VB93 Homo sapiens (Human) Amyotrophic lateral sclerosis Part of: Motor Neurone Disease (MND) collection. Transformed cell line Male ECACC 15103006 ECACC:15103006,
Wikidata:Q54955455
CVCL_VB93 2026-08-29 04:59:53 0
Sp2/0-Ag14 (serum free)
 
Resource Report
Resource Website
ECACC Cat# 08060101, RRID:CVCL_JX38 Mus musculus (Mouse) Mouse multiple myeloma Group: Serum/protein free medium cell line., Group: Hybridoma fusion partner cell line. Cancer cell line Female SP2/0-Ag14 (AC-Free) ECACC 08060101 ECACC:08060101,
Wikidata:Q54955447
cvcl_2199 CVCL_JX38 2026-08-29 04:59:52 0
SP3127
 
Resource Report
Resource Website
ECACC Cat# 15103011, RRID:CVCL_VB99 Homo sapiens (Human) Amyotrophic lateral sclerosis Part of: Motor Neurone Disease (MND) collection. Transformed cell line Female ECACC 15103011 ECACC:15103011,
Wikidata:Q54955468
CVCL_VB99 2026-08-29 04:59:53 0
SP3534
 
Resource Report
Resource Website
ECACC Cat# 15103016, RRID:CVCL_VC14 Homo sapiens (Human) Amyotrophic lateral sclerosis Part of: Motor Neurone Disease (MND) collection. Transformed cell line Female ECACC 15103016 ECACC:15103016,
Wikidata:Q54955484
CVCL_VC14 2026-08-29 04:59:54 0
SP3277
 
Resource Report
Resource Website
ECACC Cat# 15082832, RRID:CVCL_VC05 Homo sapiens (Human) Amyotrophic lateral sclerosis Part of: Motor Neurone Disease (MND) collection. Transformed cell line Male ECACC 15082832 ECACC:15082832,
Wikidata:Q54955474
CVCL_VC05 2026-08-29 04:59:53 0
SP3216
 
Resource Report
Resource Website
ECACC Cat# 15082830, RRID:CVCL_VC03 Homo sapiens (Human) Amyotrophic lateral sclerosis Part of: Motor Neurone Disease (MND) collection. Transformed cell line Female ECACC 15082830 ECACC:15082830,
Wikidata:Q54955472
CVCL_VC03 2026-08-29 04:59:59 0

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