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Cellosaurus MK-37b (CVCL_B3MD)

[Text version]
Cell line name MK-37b
Accession CVCL_B3MD
Resource Identification Initiative To cite this cell line use: MK-37b (RRID:CVCL_B3MD)
Comments Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Turner syndrome (NCIt: C26900)
Turner syndrome (ORDO: Orphanet_881)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_B3ME ! MK-37a
CVCL_LC40 ! MK-37c
Sex of cell Sex ambiguous
Age at sampling Age unspecified
Category Finite cell line
STR profile Source(s): JCRB=JCRB3069

Markers:
AmelogeninX
CSF1PO10,12
D5S81810,11
D7S82010,12
D13S3178,12
D16S53910,12
TH016,9
TPOX8,11
vWA16,18

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Cross-references
Cell line collections (Providers) JCRB; JCRB3069
JCRB; KURB2731 - Discontinued
Encyclopedic resources Wikidata; Q110433040
Entry history
Entry creation16-Dec-2021
Last entry update02-May-2024
Version number5