培养方法
传代方法 将旧培养液吸除,PBS清洗两遍后,加入6mL(/100mm皿)胰酶,在显微镜下观察,期间禁止摇晃培养皿,细胞刚有脱落时,则吸除大部分胰酶,留约0.5mL,移至培养箱消化,约2min取出。传代用12mL CM1-1培养液终止消化,轻轻吹打均匀细胞,后可分3~6皿培养;
生长条件 37℃,5%CO2,CM1-1培养液。CM1-1培养液:90%DMEM-H+10%FBS。DMEM-H:DMEM高糖培养液,含谷氨酰胺,含丙酮酸钠。
存储条件 冻存则用6mL冻存液(90%FBS+10%DMSO)终止消化,吹打均匀,分为6支冻存管,用程序降温盒于-80℃冻存,过夜转移至液氮中保存。
产品名称
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规格
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货号
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EBV 转化的绒猴白细胞
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1×106
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BH-X019746
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我司常期代理ATCC Acris abcam cst Biorbyt santa Novus sigma lifespan NEB roche ABI R&D millipore BD Qiagen Cayman Jackson Life GeneTex Bio-Rad DSHB tocris peprotech 等品牌;部分产品现货,超低比价,货期短,价格优,公司产品仅用于科研售后齐全。
培养操作步骤 :
1.用盖片镊将盖玻片自75%乙醇中取出,用无菌丝绸布擦拭干净,不要用纱布;
2.将盖玻片轻轻放入6孔培养板(每孔一片)或培养皿中(每个平皿可放置2-3片);
3.在距离紫外灯直射范围内20-30 厘米处照射2-3小时;
4.将经过计数的细胞悬浮液移入培养板中,使盖玻片完全浸在培养液中;
5.将培养板在5% CO2水浴孵箱中37℃孵育2-3天,当贴壁细胞生长至覆盖培养板底部2/3面积时,将培养板取出,用盖片镊轻轻取出盖玻片,用蒸馏水漂洗后即可进行快速固定以及细胞化学检测。
细胞培养方法:
1、细胞传代:细胞密度达到80-90%时即可传代
①弃去培养上清,用PBS或生理盐水清洗1-2次;
②加入2ml0.25%胰酶(T25瓶),使胰酶覆盖整个瓶或皿,盖好放入培养箱消化;
③1-2min后,显微镜下观察细胞,若大部分细胞回缩且有少量细胞脱落,轻轻吹打下确认消化情况后加入完全培养基终止消化;若细胞还是贴壁,放回培养箱继续消化至可以轻轻吹打下为止;
④将细胞悬液1000RPM左右条件下离心4min,弃上清;
⑤用新鲜培养基重悬后加入培养瓶或皿中,T25培养瓶加6-8ml培养基;
⑥悬浮细胞直接离心收集,细胞沉淀重悬后分到新培养瓶中。
2、细胞复苏:
①将冻存管在37℃温水中快速摇晃融化,时间1min左右,加入4-5ml培养基混匀。
②在1000RPM左右条件下离心4min,弃上清,加1-2ml培养基吹匀,将细胞悬液加入培养瓶中,补加适量培养基。
3、细胞冻存:待细胞生长状态良好时进行细胞冻存保种
①弃去培养上清,用PBS或生理盐水清洗1-2次,加入1mL 0.25%胰蛋白酶(T25瓶)
②1-2min后,显微镜下观察细胞,大部分细胞回缩且有少量细胞脱落,轻轻吹打下确认消化情况后加入完全培养基终止消化;
③将细胞悬液1000RPM左右条件下离心4min,弃上清,加1ml冻存液重悬细胞;
④将冻存管放入程序降温盒,放入-80℃冰箱,4小时后将冻存管转入液氮罐储存。
研究领域 细胞生物 发育生物学 干细胞
蛋白分子量 predicted molecular weight: 119kDa
性 状 Lyophilized or Liquid
免 疫 原 KLH conjugated synthetic peptide derived from Human PMFBP1
亚 型 IgG
纯化方法 affinity purified by Protein A
储 存 液 Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4
产品应用 WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500
(石蜡切片需做抗原修复)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
保存条件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
Important Note This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
产品介绍 PMF-1 is a 205 amino acid protein involved in kinetochore formation. Localized to the nucleus, PMF-1 contains a coiled-coil domain which interacts with the leucine-zipper domain of Nrf2. This interaction regulates the transcription of SSAT, a regulatory enzyme for polyamine catabolism. PMF-1 is also a component of the MIS12 complex, which is required for kinetochore formation and chromosomal alignment and segregation. PMF-1 is expressed at highest levels in skeletal muscle and heart, with moderate expression in liver and kidney. PMFBP1 (Polyamine-modulated factor 1-binding protein 1) is a 1022 amino acid protein that binds PMF-1 and may be involved in general organization of the cytoskeleton. Due to evidence that PMFBP1 may play a role in sperm tail morphology, it may therefore affect fertility. There are three isoforms of PMFBP1 that are produced as a result of alternative splicing events.
Function : May play a role in sperm morphology especially the sperm tail and consequently affect fertility. May also be involved in the general organization of cellular cytoskeleton.Target information above from: UniProt accession Q8TBY8 The UniProt Consortium The Universal Protein Resource (UniProt) in 2010 Nucleic Acids Res. 38:D142-D148 (2010).
Database links : UniProtKB/Swiss-Prot: Q8TBY8.1
英文名称 Anti-PBX3
中文名称 B细胞白血病前体蛋白转录因子3抗体
EBV 转化的绒猴白细胞视黄结合蛋白检测试剂盒异辛 standard for GC, ≥99.5% (GC)黄色氧化铅 99.999% metals basis
视黄结合蛋白4检测试剂盒异辛 AR2-氨基-3,4-二甲酸 98%
视黄酸检测试剂盒异辛 CP反式-(1R,2R)-2-氨基环戊盐酸盐 97%
视锥蛋白样蛋白1检测试剂盒异辛 >99.0%(GC)反式-(1S,2S)-2-氨基环戊盐酸盐 98%
嗜铬粒蛋白A检测试剂盒异辛 分析标准品,≥99.5%顺式-(1R,2S)-2-氨基环戊盐酸盐 98%
嗜环蛋白;亲环素A检测试剂盒苯甲酸乙酯 GCS,>99.5%(GC)3-氨基巴豆酸甲酯 97%
嗜环蛋白;亲环素B检测试剂盒苯甲酸乙酯 AR,99%(S)-3-氨基-1,2- 98%
实验要点及说明:
1.本方法适用于贴壁细胞培养,而不适用于悬浮细胞培养,悬浮细胞可使用滴片法;
2.所使用的盖玻片应该为玻璃**,并经过铬酸洗液处理;
3.盖玻片非常薄,易碎,取放盖玻片时动作要轻;
4.如果需要更多生长状态一致的细胞,可以使用较大的培养皿,但不宜过大,以避免培养液的浪费和增加污染机率;
5.如果细胞贴壁生长能力较差,可将盖玻片在0.5%多聚赖氨酸溶液中浸泡5-10分钟并自然晾干。