Searching the RRID Resource Information Network

Our searching services are busy right now. Please try again later

  • Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes

Preparing word cloud

×

Suggested Search Criteria

Enter extra filters to help narrow your search

Search

Type in a keyword to search

Filter by records added date
See new records

Options


Current Facets and Filters

  • Vendor:ecacc (facet)

Facets


Recent searches

Snippet view Table view
Click the to add this resource to an Authentication Report or Collection

6,967 Results - per page

Show More Columns | Download Top 1000 Results

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
DD3344
 
Resource Report
Resource Website
ECACC Cat# 99010601, RRID:CVCL_9P38 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 99010601 ECACC:99010601,
Wikidata:Q54830706
CVCL_9P38 2026-07-25 04:30:13 0
DD3422
 
Resource Report
Resource Website
ECACC Cat# 99060719, RRID:CVCL_9P64 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 99060719 ECACC:99060719,
Wikidata:Q54830742
CVCL_9P64 2026-07-25 04:30:14 0
DD3373
 
Resource Report
Resource Website
ECACC Cat# 99031005, RRID:CVCL_9N02 Homo sapiens (Human) Prader-Willi syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 99031005 ECACC:99031005,
Wikidata:Q54830716
CVCL_9N02 2026-07-25 04:30:14 0
DD3375
 
Resource Report
Resource Website
ECACC Cat# 99031814, RRID:CVCL_9P44 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 99031814 ECACC:99031814,
Wikidata:Q54830718
CVCL_9P44 2026-07-25 04:30:13 0
DD3458
 
Resource Report
Resource Website
ECACC Cat# 99802743, RRID:CVCL_9N09 Homo sapiens (Human) Karyotypic information: 46,XY,inv(12)?(p11.21;q21.2); de novo (ECACC=99802743)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 99802743 ECACC:99802743,
Wikidata:Q54830752
CVCL_9N09 2026-07-25 04:30:14 0
DD3372
 
Resource Report
Resource Website
ECACC Cat# 99030917, RRID:CVCL_9N01 Homo sapiens (Human) Type 1 diabetes mellitus Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 99030917 ECACC:99030917,
Wikidata:Q54830715
CVCL_9N01 2026-07-25 04:30:13 0
DD3390
 
Resource Report
Resource Website
ECACC Cat# 99033111, RRID:CVCL_9P54 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 99033111 ECACC:99033111,
Wikidata:Q54830728
CVCL_9P54 2026-07-25 04:30:14 0
DD3445
 
Resource Report
Resource Website
ECACC Cat# 99071438, RRID:CVCL_9P67 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 99071438 ECACC:99071438,
Wikidata:Q54830747
CVCL_9P67 2026-07-25 04:30:14 0
DD3421
 
Resource Report
Resource Website
ECACC Cat# 99060718, RRID:CVCL_9P63 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 99060718 ECACC:99060718,
Wikidata:Q54830741
CVCL_9P63 2026-07-25 04:30:14 0
DD3454
 
Resource Report
Resource Website
ECACC Cat# 99081610, RRID:CVCL_9P68 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 99081610 ECACC:99081610,
Wikidata:Q54830750
CVCL_9P68 2026-07-25 04:30:14 0
DD3420
 
Resource Report
Resource Website
ECACC Cat# 99060428, RRID:CVCL_9N04 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 99060428 ECACC:99060428,
Wikidata:Q54830740
CVCL_9N04 2026-07-25 04:30:14 0
DD3341
 
Resource Report
Resource Website
ECACC Cat# 98122307, RRID:CVCL_9M96 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98122307 ECACC:98122307,
Wikidata:Q54830705
CVCL_9M96 2026-07-25 04:30:13 0
DD3409
 
Resource Report
Resource Website
ECACC Cat# 99051707, RRID:CVCL_9P57 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 99051707 ECACC:99051707,
Wikidata:Q54830732
CVCL_9P57 2026-07-25 04:30:14 0
DD3359
 
Resource Report
Resource Website
ECACC Cat# 99021505, RRID:CVCL_9P40 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 99021505 ECACC:99021505,
Wikidata:Q54830711
CVCL_9P40 2026-07-25 04:30:13 0
DD3365
 
Resource Report
Resource Website
ECACC Cat# 99021917, RRID:CVCL_9P42 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 99021917 ECACC:99021917,
Wikidata:Q54830714
CVCL_9P42 2026-07-25 04:30:13 0
DD3364
 
Resource Report
Resource Website
ECACC Cat# 99021916, RRID:CVCL_9P41 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 99021916 ECACC:99021916,
Wikidata:Q54830713
CVCL_9P41 2026-07-25 04:30:13 0
DD3362
 
Resource Report
Resource Website
ECACC Cat# 99021607, RRID:CVCL_9N00 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 99021607 ECACC:99021607,
Wikidata:Q54830712
CVCL_9N00 2026-07-25 04:30:13 0
DD3377
 
Resource Report
Resource Website
ECACC Cat# 99031903, RRID:CVCL_9P46 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 99031903 ECACC:99031903,
Wikidata:Q54830720
CVCL_9P46 2026-07-25 04:30:13 0
DD3416
 
Resource Report
Resource Website
ECACC Cat# 99060203, RRID:CVCL_9P59 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 99060203 ECACC:99060203,
Wikidata:Q54830734
CVCL_9P59 2026-07-25 04:30:14 0
DD3354
 
Resource Report
Resource Website
ECACC Cat# 99020323, RRID:CVCL_9P39 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 99020323 ECACC:99020323,
Wikidata:Q54830708
CVCL_9P39 2026-07-25 04:30:13 0

Can't find your Cell Line?

We recommend that you click next to the search bar to check some helpful tips on searches and refine your search firstly. If you want to find a specific cell line, it's easier to enter an RRID or add the vendor information to search. You can refine the search results using Facets on the left side of the search results page. If you are on the table view, you can also search in a specific column by clicking the column title and enter the keywords.

If you still could not find your cell line in the search results, please help us by registering it into the system — it's easy. Register it with the Cellosaurus. An RRID will be generated in 1-2 business days.

Can't find the RRID you're searching for? X
X
  1. Neuroscience Information Framework Resources

    Welcome to the NIF Resources search. From here you can search through a compilation of resources used by NIF and see how data is organized within our community.

  2. Navigation

    You are currently on the Community Resources tab looking through categories and sources that NIF has compiled. You can navigate through those categories from here or change to a different tab to execute your search through. Each tab gives a different perspective on data.

  3. Logging in and Registering

    If you have an account on NIF then you can log in from here to get additional features in NIF such as Collections, Saved Searches, and managing Resources.

  4. Searching

    Here is the search term that is being executed, you can type in anything you want to search for. Some tips to help searching:

    1. Use quotes around phrases you want to match exactly
    2. You can manually AND and OR terms to change how we search between words
    3. You can add "-" to terms to make sure no results return with that term in them (ex. Cerebellum -CA1)
    4. You can add "+" to terms to require they be in the data
    5. Using autocomplete specifies which branch of our semantics you with to search and can help refine your search
  5. Collections

    If you are logged into NIF you can add data records to your collections to create custom spreadsheets across multiple sources of data.

  6. Facets

    Here are the facets that you can filter the data by.

  7. Further Questions

    If you have any further questions please check out our FAQs Page to ask questions and see our tutorials. Click this button to view this tutorial again.