Traditional DNA/RNA isolation kits can be used to prepare genomic material for sequencing (RNA-seq, scRNA-seq, WGS, CHIP-seq etc). For some applications with large organoids, tissue specific DNA/RNA extraction kits are recommended. TRI Reagent (T9424) can be added to the dissociated organoids before RNA extraction and can be stored at -80 °C until future use.
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| Size/SKU | Availability | Price |
|---|---|---|
50 mL | Available to ship TODAYfromAreál Kühne+Nagel spol. s r.o. | CZK 9,340.00 |
About This Item
CZK 9,340.00
Available to ship TODAYDetails
form
liquid
packaging
pkg of 50 mL
technique(s)
cell culture | stem cell: suitable
osmolality
350-375 mOsm
application(s)
cell analysis
General description
Application
Research Category:
- Cell Culture
- Stem Cell Research
Preparation Note
Analysis Note
Osmolality: 350-375 mOsm
pH: 7.0 – 7.4
Sterility Tested: No Growth/Pass
Endotoxin: <2 EU/mL
Mycoplasma: Negative
Functional Assay: Thaw and culture of human colon organoids for 2 passages.
Legal Information
Disclaimer
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This Item | |
|---|---|
| technique(s) cell culture | stem cell: suitable | technique(s) cell culture | stem cell: suitable |
| form liquid | form liquid |
| application(s) cell analysis | application(s) - |
| packaging pkg of 50 mL | packaging - |
| osmolality 350-375 mOsm | osmolality - |
Storage Class
12 - Non Combustible Liquids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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How Do you Extract RNA/DNA from Organoids in Cultured in Matrigel?
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How do you stain organoids with antibodies?
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Organoids can be stained with antibodies for immunocytochemical (ICC)/Immunohistochemical (IHC) analysis using either whole-mount or paraffin embedding/sectioning techniques. It is critical to use antibodies prequalified for organoid analysis.
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How are organoids cultured?
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Once isolated, organoids are cultured in specialized media embedded in a rich extracellular matrix (ECM) basement membrane extract hydrogel such as Growth Factor Reduced Matrigel. Media is replenished every other day and cells are passaged once per week (7-12 days) before cells become too large or necrotic. Cells can be passaged in either small clump fragments or as single cells using mechanical dissociation/enzyme-free passaging reagents. Depending on organoid type and confluency, split ratios of roughly 1:3-1:4 can be used when passaging organoids. For sensitive organoid types, ROCKi (Y27632) (SCM075) can be added during passaging to help in promoting cell viability.
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