MM138 cell line细胞株-BioVector NTCC质粒载体菌株细胞蛋白抗体基因保藏中心
- 价 格:¥79865
- 货 号:BioVector-CBA-1345
- 产 地:北京
- BioVector NTCC典型培养物保藏中心
- 联系人:Dr.Xu, Biovector NTCC Inc.
电话:400-800-2947 工作QQ:1843439339 (微信同号)
邮件:Biovector@163.com
手机:18901268599
地址:北京
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Description: Melanoma cell line from lymph node
Description Key Words: Human melanoma
Also Known As: No other names
Organism: Human (Homo sapiens)
Tissue: Skin
Growth Properties: Adherent
Morphology: Epithelial
Growth Medium: RPMI 1640 (with 2mM L-Glutamine + 25mM Hepes) + 10% Foetal Calf Serum (FCS)
Resuscitation: Remove protective cryoflex layer around the ampoule prior to thawing. Thaw the ampoule by gently agitating in a 37°C waterbath; thawing should be rapid (around 2 minutes). A centrifugation step to remove the cryoprotectant after thawing is necessary for this cell line.
Subculturing Procedure:
Medium Renewal:
Subcultivation Ratio: 1:4, Seeding density 0.8 x104 cells/cm2. Harvest the cells using 0.05% Trypsin/EDTA at 37°C for 5 min. MM138 has a relatively slow doubling time of around 60 hours. It does not become confluent and will detach after 6-7 days. If split too hard, the doubling time is greatly increased.
Culture Conditions: Cells incubated at 37°C with 5% CO2.
Cryoprotectant Medium: 10% DMSO + 90% FCS
Handling Procedure for Frozen Cells: Upon receipt, frozen ampoules should be transferred directly to liquid nitrogen storage without delay, if not to be used immediately. Storage at -80°C may result in loss of viability.
Additional Information:
Mutations:
- Homozygous deletion CDKN2A.
Medium:
Growth Condition:
BioVector NTCC Inc.
www.biovector.net
Description Key Words: Human melanoma
Also Known As: No other names
Organism: Human (Homo sapiens)
Tissue: Skin
Growth Properties: Adherent
Morphology: Epithelial
Growth Medium: RPMI 1640 (with 2mM L-Glutamine + 25mM Hepes) + 10% Foetal Calf Serum (FCS)
Resuscitation: Remove protective cryoflex layer around the ampoule prior to thawing. Thaw the ampoule by gently agitating in a 37°C waterbath; thawing should be rapid (around 2 minutes). A centrifugation step to remove the cryoprotectant after thawing is necessary for this cell line.
Subculturing Procedure:
Medium Renewal:
Subcultivation Ratio: 1:4, Seeding density 0.8 x104 cells/cm2. Harvest the cells using 0.05% Trypsin/EDTA at 37°C for 5 min. MM138 has a relatively slow doubling time of around 60 hours. It does not become confluent and will detach after 6-7 days. If split too hard, the doubling time is greatly increased.
Culture Conditions: Cells incubated at 37°C with 5% CO2.
Cryoprotectant Medium: 10% DMSO + 90% FCS
Handling Procedure for Frozen Cells: Upon receipt, frozen ampoules should be transferred directly to liquid nitrogen storage without delay, if not to be used immediately. Storage at -80°C may result in loss of viability.
Additional Information:
Mutations:
- Homozygous deletion CDKN2A.
Medium:
Growth Condition:
BioVector NTCC Inc.
www.biovector.net
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