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W3/13杂交瘤细胞Hybridoma cells BioVector NTCC保藏中心
Reactibity反应性:Anti- CD43, rat
Antibody Isotype抗体类性:IgG1
【Organism物种来源】Mouse
【Tissue组织来源】
【Cell Type: 细胞类型】 Hybridoma
【Product Format产品状态】 frozen/live culture
【Morphology细胞形态】
【Culture Properties细胞特性】
【Biosafety Level生物安全级别】 1/2
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.
Myeloma:
Fusion Species: Mouse x Mouse Hybridoma
【Immunogen:】
【Cell Line Description:】
【Storage Conditions保存条件】 liquid nitrogen vapor phase
【Karyotype染色体组型】
【Images细胞图片】 Cell Micrograph
【Derivation衍生细胞】
【Clinical Data临床数据】
【Comments其他描述】
【Complete Growth Medium完全培养基】DMEM + 2mM glutamine + 20% Foetal Bovine Serum (FBS)
【Subculturing传代方法】
Maintain cultures between 3-9x100,000 cells/ml; 5% CO2; 37°C. When recovering hybridoma cultures from frozen it is not unusual for growth to be slower than expected initially and there may be an observed decrease in viability. Establishment of an actively proliferating culture may take up to 2 weeks. On resuscitation a centrifugation step to remove the cryoprotectant is essential. Rapidly thaw the frozen ampoule in a water bath at 37°C for 1-2 minutes. Transfer the contents to a centrifuge tube and slowly add 5-10ml of prewarmed growth media+. Remove a sample for counting. Centrifuge at 100 x g for 2-3 minutes to pellet cells and seed at a relatively high density of 5-7 x 10⁵ cells/ml. Place culture flask flat and observe regularly until viable proliferating cells are seen. Often hybridoma cultures may benefit from being resuspended with media supplemented with 20% FBS in the early critical stage of culture establishment immediately post resuscitation. Once the culture is established in culture the FBS can be reduced to 10%.
【Cryopreservation冻存条件】
【Freeze Medium冻存培养基】Complete growth medium supplemented with 5% (v/v) DMSO
【Storage Temperature保存温度】 Liquid nitrogen vapor phase
【Culture Conditions培养条件】
【Atmosphere培养环境】 Air, 95%; carbon dioxide (CO2), 5%
【Temperature培养温度】 37°C
【STR Profile图谱】
【Population Doubling Time倍增殖时间】
【References参考文献】
【Supplier细胞供应厂家】BioVector NTCC Inc.
TEL:+86-010-53513060
【Website网址】http://www.biovector.net
Reactibity反应性:Anti- CD43, rat
Antibody Isotype抗体类性:IgG1
【Organism物种来源】Mouse
【Tissue组织来源】
【Cell Type: 细胞类型】 Hybridoma
【Product Format产品状态】 frozen/live culture
【Morphology细胞形态】
【Culture Properties细胞特性】
【Biosafety Level生物安全级别】 1/2
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.
Myeloma:
Fusion Species: Mouse x Mouse Hybridoma
【Immunogen:】
【Cell Line Description:】
【Storage Conditions保存条件】 liquid nitrogen vapor phase
【Karyotype染色体组型】
【Images细胞图片】 Cell Micrograph
【Derivation衍生细胞】
【Clinical Data临床数据】
【Comments其他描述】
【Complete Growth Medium完全培养基】DMEM + 2mM glutamine + 20% Foetal Bovine Serum (FBS)
【Subculturing传代方法】
Maintain cultures between 3-9x100,000 cells/ml; 5% CO2; 37°C. When recovering hybridoma cultures from frozen it is not unusual for growth to be slower than expected initially and there may be an observed decrease in viability. Establishment of an actively proliferating culture may take up to 2 weeks. On resuscitation a centrifugation step to remove the cryoprotectant is essential. Rapidly thaw the frozen ampoule in a water bath at 37°C for 1-2 minutes. Transfer the contents to a centrifuge tube and slowly add 5-10ml of prewarmed growth media+. Remove a sample for counting. Centrifuge at 100 x g for 2-3 minutes to pellet cells and seed at a relatively high density of 5-7 x 10⁵ cells/ml. Place culture flask flat and observe regularly until viable proliferating cells are seen. Often hybridoma cultures may benefit from being resuspended with media supplemented with 20% FBS in the early critical stage of culture establishment immediately post resuscitation. Once the culture is established in culture the FBS can be reduced to 10%.
【Cryopreservation冻存条件】
【Freeze Medium冻存培养基】Complete growth medium supplemented with 5% (v/v) DMSO
【Storage Temperature保存温度】 Liquid nitrogen vapor phase
【Culture Conditions培养条件】
【Atmosphere培养环境】 Air, 95%; carbon dioxide (CO2), 5%
【Temperature培养温度】 37°C
【STR Profile图谱】
【Population Doubling Time倍增殖时间】
【References参考文献】
【Supplier细胞供应厂家】BioVector NTCC Inc.
TEL:+86-010-53513060
【Website网址】http://www.biovector.net
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