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ZF4
ZF4
规格:
货期:
编号:TS210622
品牌:Testobio
产品名称: ZF4
商品货号: TS210622
Organism: Danio rerio, zebrafish
Tissue:
embryo
Product Format: frozen
Morphology: fibroblast
Culture Properties: adherent
Biosafety Level: 1

Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.

Age: 1 day old embryo
Applications:
The cells can be used as a transfection host.
Storage Conditions: liquid nitrogen vapor phase
Karyotype: hyperploid; range = 110 to 120
Images:
Derivation:
The ZF4 cell line was established from 1-day-old zebrafish embryos.
Comments:

The ZF4 cell line was established from 1-day-old zebrafish embryos.

The cells are cultivated at 28°C.
ZF4 cells are killed within 10 days by culturing in medium containing 0.8 to 1.0 mg/mL G418.
Complete Growth Medium: The base medium for this cell line is ATCC-formulated DMEM:F12 Medium Catalog No. 30-2006. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
Subculturing:
Volumes are given for a 75 cm2 flask. Increase or decrease the amount of dissociation medium needed proportionally for culture vessels of other sizes.
  1. Remove and discard culture medium.
  2. Briefly rinse the cell layer with 0.25% (w/v) Trypsin solution to remove all traces of serum that contains trypsin inhibitor.
  3. Add 2.0 to 3.0 mL of Trypsin solution to flask and observe cells under an inverted microscope until cell layer is dispersed (usually within 5 to 15 minutes).
  4. Add 6.0 to 8.0 mL of complete growth medium and aspirate cells by gently pipetting.
  5. Add appropriate aliquots of the cell suspension to new culture vessels.
  6. Incubate cultures at 28°C.

NOTE:xa0DO NOT USExa0EDTA TO DISSOCIATE THExa0CELLS.

Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:4 is recommended
Medium Renewal: 2 to 3 times per week
Cryopreservation:
Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO
Storage temperature: liquid nitrogen vapor phase
Culture Conditions:
Atmosphere: air, 95%; carbon dioxide (CO2), 5%
Temperature: 28°C
Name of Depositor: W Driever
Deposited As: Brachydanio rerio
References:

Driever W, Rangini Z. Characterization of a cell line derived from zebrafish (Brachydanio rerio) embryos. In Vitro Cell. Dev. Biol. Anim. 29A: 749-754, 1993. PubMed: 8407719

Biosafety in Microbiological and Biomedical Laboratories 4th ed.; U.S. Department of Health and Human Services ;1999.

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ZF4

  • 货号: TS210622
  • 好评
询价
  • 品牌 : TESTOBIO
产品名称: ZF4
商品货号: TS210622
Organism: Danio rerio, zebrafish
Tissue:
embryo
Product Format: frozen
Morphology: fibroblast
Culture Properties: adherent
Biosafety Level: 1

Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.

Age: 1 day old embryo
Applications:
The cells can be used as a transfection host.
Storage Conditions: liquid nitrogen vapor phase
Karyotype: hyperploid; range = 110 to 120
Images:
Derivation:
The ZF4 cell line was established from 1-day-old zebrafish embryos.
Comments:

The ZF4 cell line was established from 1-day-old zebrafish embryos.

The cells are cultivated at 28°C.
ZF4 cells are killed within 10 days by culturing in medium containing 0.8 to 1.0 mg/mL G418.
Complete Growth Medium: The base medium for this cell line is ATCC-formulated DMEM:F12 Medium Catalog No. 30-2006. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
Subculturing:
Volumes are given for a 75 cm2 flask. Increase or decrease the amount of dissociation medium needed proportionally for culture vessels of other sizes.
  1. Remove and discard culture medium.
  2. Briefly rinse the cell layer with 0.25% (w/v) Trypsin solution to remove all traces of serum that contains trypsin inhibitor.
  3. Add 2.0 to 3.0 mL of Trypsin solution to flask and observe cells under an inverted microscope until cell layer is dispersed (usually within 5 to 15 minutes).
  4. Add 6.0 to 8.0 mL of complete growth medium and aspirate cells by gently pipetting.
  5. Add appropriate aliquots of the cell suspension to new culture vessels.
  6. Incubate cultures at 28°C.

NOTE:xa0DO NOT USExa0EDTA TO DISSOCIATE THExa0CELLS.

Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:4 is recommended
Medium Renewal: 2 to 3 times per week
Cryopreservation:
Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO
Storage temperature: liquid nitrogen vapor phase
Culture Conditions:
Atmosphere: air, 95%; carbon dioxide (CO2), 5%
Temperature: 28°C
Name of Depositor: W Driever
Deposited As: Brachydanio rerio
References:

Driever W, Rangini Z. Characterization of a cell line derived from zebrafish (Brachydanio rerio) embryos. In Vitro Cell. Dev. Biol. Anim. 29A: 749-754, 1993. PubMed: 8407719

Biosafety in Microbiological and Biomedical Laboratories 4th ed.; U.S. Department of Health and Human Services ;1999.

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