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Key Documents

H6909

Sigma-Aldrich

Hydrocortisone solution

50 μM, sterile-filtered, BioXtra, suitable for cell culture

Synonym(s):

17-Hydroxycorticosterone, Cortisol

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About This Item

CAS Number:
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.77

biological source

non-animal source

sterility

sterile-filtered

product line

BioXtra

form

liquid

concentration

50 μM

technique(s)

cell culture | mammalian: suitable

impurities

endotoxin, tested

pH

5.0- 7.0

shipped in

dry ice

storage temp.

−20°C

SMILES string

C[C@]12CCC(=O)C=C1CC[C@H]3[C@@H]4CC[C@](O)(C(=O)CO)[C@@]4(C)C[C@H](O)[C@H]23

InChI

1S/C21H30O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h9,14-16,18,22,24,26H,3-8,10-11H2,1-2H3/t14-,15-,16-,18+,19-,20-,21-/m0/s1

InChI key

JYGXADMDTFJGBT-VWUMJDOOSA-N

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Application

Hydrocortisone has been used in epithelial and endothelial adherent cell culture applications. Hydrocortisone solution has been used for the isolation of epidermal stem cells and cell expansion. It has also been used for keratinocyte permeability assay.

Other Notes

Animal-component free

Physical form

frozen in working aliquots, avoid repeated freeze/thaw

Related product

Product No.
Description
Pricing

Storage Class

12 - Non Combustible Liquids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificates of Analysis (COA)

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Natalja E Fedorovich et al.
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Matrix metalloproteinases (MMPs) play a crucial role in the malignant phenotype of cancer cells. In particular, active levels of MMP2 in cancer cells have been associated with invasion and metastasis through the degradation of basement membrane extracellular matrix proteins. However
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The skin is susceptible to different injuries and diseases. One major obstacle in skin tissue engineering is how to develop functional three-dimensional (3D) substitute for damaged skin. Previous studies have proved a 3D dynamic simulated microgravity (SMG) culture system as
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Here, we present a standardized protocol for isolation, maintenance, and polarization of the respiratory epithelial primary cells from patient samples acquired from nasal brushing, polyp specimens, or lung explants. This protocol generates a clearly defined polarized layer of epithelial cells

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