ARPE-19人视网膜上皮细胞

ARPE-19人视网膜上皮细胞

2024-08-13更新 | 121次浏览 | 121次下载 | .docx
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ARPE-19 人视网膜上皮细胞

 

 

ARPE-19人视网膜上皮细胞说明书

General Information:

Organism:

Homo sapiens, human

Tissue:

retinal pigmented epithelium; retina

Culture Properties:

adherent

Morphology:

epithelial

Culture Method:

Complete Growth Medium:

DMEM(Gibco 12800-017)+10% FBS+Penicillin/Streptomycin

Subculturing:

Volumes are given for a 25cm2flask. Increase or decrease the amount of dissociation medium needed proportionally for culture vessels of other sizes.

Remove and discard culture medium.

Briefly rinse the cell layer with 0.25%(w/v) Trypsin-0.53 mM EDTA solution to remove all traces of serum that contains trypsin inhibitor.

Add 1.0 to 2.0mL of Trypsin-EDTA solution to flask and observe cells under an inverted microscope until cell layer is dispersed.DiscardTrypsin-EDTA solution.

Add 6.0 to 8.0mL of complete growth medium and aspirate cells by gently pipetting.

Add appropriate aliquots of the cell suspension to new culture vessels.

Incubate cultures at 37°C, 5% CO2.

Subcultivation Ratio:

A subcultivation ratio of 1:3to 1:5is recommended

Cryopreservation:

Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO

Storage temperature: liquid nitrogen vapor phase

 

ARPE-19人视网膜上皮细胞

ARPE-19人视网膜上皮细胞


 

ARPE-19 人视网膜上皮细胞

 

 

ARPE-19人视网膜上皮细胞说明书

General Information:

Organism:

Homo sapiens, human

Tissue:

retinal pigmented epithelium; retina

Culture Properties:

adherent

Morphology:

epithelial

Culture Method:

Complete Growth Medium:

DMEM(Gibco 12800-017)+10% FBS+Penicillin/Streptomycin

Subculturing:

Volumes are given for a 25cm2flask. Increase or decrease the amount of dissociation medium needed proportionally for culture vessels of other sizes.

Remove and discard culture medium.

Briefly rinse the cell layer with 0.25%(w/v) Trypsin-0.53 mM EDTA solution to remove all traces of serum that contains trypsin inhibitor.

Add 1.0 to 2.0mL of Trypsin-EDTA solution to flask and observe cells under an inverted microscope until cell layer is dispersed.DiscardTrypsin-EDTA solution.

Add 6.0 to 8.0mL of complete growth medium and aspirate cells by gently pipetting.

Add appropriate aliquots of the cell suspension to new culture vessels.

Incubate cultures at 37°C, 5% CO2.

Subcultivation Ratio:

A subcultivation ratio of 1:3to 1:5is recommended

Cryopreservation:

Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO

Storage temperature: liquid nitrogen vapor phase

 

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