- ¥1558
- Invitrogen™ eBioscience™
- 00-5523-00
- Invitrogen™ eBioscience™ Foxp3 / Transcription Factor Staining Buffer Set 00-5523-00
- 2025年08月02日
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- 详细信息
- 询价记录
- 文献和实验
- 技术资料
- 库存：
Invitrogen™ eBioscience™ Foxp3 / Transcription Factor Staining Buffer Set 00-5523-00
- 英文名：
Invitrogen™ eBioscience™ Foxp3 / Transcription Factor Staining Buffer Set 00-5523-00
- CAS号：
Invitrogen™ eBioscience™ Foxp3 / Transcription Factor Staining Buffer Set 00-5523-00
- 保质期：
Invitrogen™ eBioscience™ Foxp3 / Transcription Factor Staining Buffer Set 00-5523-00
- 供应商：
上海辅泽商贸有限公司
- 保存条件：
Invitrogen™ eBioscience™ Foxp3 / Transcription Factor Staining Buffer Set 00-5523-00
- 规格：
1 kit
货号： 00-5523-00
相关应用：流式细胞术
| 细胞成像
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| 货号 | 单位规格 | 单价 (CNY) | 数量 | |
|---|---|---|---|---|
| 00-5523-00 | 1 kit | 1,558.00 |
规格
| Prop-65 Warning: | Control Code 65 |
|---|---|
| Product Line: | eBioscience™ |
| Product Size: | 1 kit |
| Reagent Type: | Fixation Diluent, Fixation Reagent, Permeabilization Diluent, Permeabilization Reagent |
描述
Foxp3/Transcription Factor Staining Buffer Set 专利配方设计和优化，可使用抗体对转录因子和核蛋白（例如 Foxp3 和 Ki-67）以及细胞因子和趋化因子进行核内染色。请参阅“最佳方案”部分了解更多信息。
For Research Use Only. Not for use in diagnostic procedures.
图表
Human Foxp3 detected using Foxp3/Transcription Factor Staining Buffer Set
Mouse Nanog detected using Foxp3/Transcription Factor Staining Buffer Set
Mouse Foxp3 detected using Foxp3/Transcription Factor Staining Buffer Set
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文献和实验microspheres = count (1 corner of 4 x 4 section) x (1 x 104 ) x (dilution factor) x (resuspension volume in mL) 31.Store coupled microspheres refrigerated at 2-8°C in the dark. Technical Note 1 : For a list of magnetic separators, see Recommended
A general protocol for staining cell for cytometry analysis
General Annexin V Staining Procedure Solutions 1.10X Binding Buffer (Cat. No. 66121A):0.1 M HEPES, pH 7.4; 1.4 M NaCl; 25 mM CaCl 2 . Dilute to 1× prior to use. 2. Propidium Iodide (PI). Prepare a 50 µg/ml stock solution of PI in 1× PBS buffer
A general protocol for staining cell for cytometry analysis
Staining 1. Wash cells twice with cold PBS and then resuspend cells in 1X Binding Buffer at a concentration of ~1 x 10 6 cells/ml. 2. Transfer 100 µl of the solution (~1 x 10 5 cells) to a 5 ml culture
