用户验证的应用
经验证应用
| 项目 | 详情 |
|---|---|
| Application | Intracellular staining (flow cytometry) (Routinely Tested), Fluorescence microscopy, Immunohistochemistry-frozen (Tested During Development) |
推荐实验流程
This product is NOT recommended to use with BrdU flow kits, e.g. Cat. No. 559619. Please see the detailed protocol under "Cell Cycle/DNA Analysis" at our website: www.bdbiosciences.com/resources/index.jsp
详细信息
制备与储存
Store undiluted at 4°C. The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography.
荧光格式说明
Tissue culture supernatant is purified by either protein A/G or affinity purification methods. Both methods yield antibody in solution that is free of most other soluble proteins, lipids, etc. This format provides pure antibody that is suitable for a number of downstream applications including: secondary labeling for flow cytometry or microscopy, ELISA, Western blot, etc.
产品提示
Since applications vary, each investigator should titrate the reagent to obtain optimal results., An isotype control should be used at the same concentration as the antibody of interest., Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing., Sodium azide is a reversible inhibitor of oxidative metabolism; therefore, antibody preparations containing this preservative agent must not be used in cell cultures nor injected into animals. Sodium azide may be removed by washing stained cells or plate-bound antibody or dialyzing soluble antibody in sodium azide-free buffer. Since endotoxin may also affect the results of functional studies, we recommend the NA/LE (No Azide/Low Endotoxin) antibody format, if available, for in vitro and in vivo use., Species cross-reactivity detected in product development may not have been confirmed on every format and/or application., Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
背景信息
Bromodeoxyuridine (BrdU) is an analog of thymidine that can be incorporated into newly synthesized DNA by cells entering and progressing through the DNA synthesis (S) phase of the cell cycle. The amount of incorporated BrdU depends on the amount of time that the cells are exposed to BrdU (pulse time), the rate of cell division, and whether the cells are in early, mid, or late S phase. Investigators can identify cycling cells in an asynchronous cell population and determine cell cycle kinetics by detecting incorporated BrdU. The 3D4 monoclonal antibody reacts with BrdU, but not other nucleotides, in single-stranded DNA. Random cleavage (nicking) of cellular DNA with DNase I permits the binding of the antibody to incorporated BrdU.
文献引用 (69)
DNA2 enables growth by restricting recombination-restarted replication.
DNA2 通过限制重组重启复制来促进生长。
Single cell suppression profiling of human regulatory T cells
人类调节性T细胞的单细胞抑制谱分析
Androgen receptor-regulated lncRNA PRCAT71 promotes AR signaling through the interaction with KHSRP in prostate cancer.
雄激素受体调控的lncRNA PRCAT71通过与KHSRP相互作用促进前列腺癌中的AR信号传导
Evolutionarily recent transcription factors partake in human cell cycle regulation
进化上较新的转录因子参与人类细胞周期调控。
Long-range enhancer-controlled genes are hypersensitive to regulatory factor perturbations.
长程增强子控制的基因对调控因子扰动高度敏感
The CBS/H2S axis regulates intestinal stem cell homeostasis and radiation-induced intestinal damage
CBS/H2S轴调节肠道干细胞稳态和辐射引起的肠道损伤。
Molecular and genetic evidence for the role of AMBRA1 in suppressing S-phase entry and tumorigenesis
分子和遗传证据表明 AMBRA1 在抑制 S 期进入和肿瘤发生中发挥作用
Molecular differences between young and mature stria vascularis from organotypic explants and transcriptomics
器官型外植体和转录组学中年轻和成熟血管纹之间的分子差异
Reduction of intestinal RIPK1 ameliorates HFD-induced metabolic disorders in female mice
肠道 RIPK1 的减少可改善雌性小鼠 HFD 诱发的代谢紊乱
Assessing Human Treg Suppression at Single-Cell Resolution Using Mass Cytometry
利用质谱流式细胞术在单细胞分辨率下评估人Treg细胞的抑制作用
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