Anti-BrdU抗体[MoBu-1]
参阅全部 BrdU 一抗
小鼠单克隆抗体[MoBu-1] to BrdU
Mouse
This antibody reacts specifically with BrdU incorporated into DNA during S-phase of a cell cycle. It is useful for detecting proliferating cells by flow cytometry or immunofluorescence staining. The reaction shows a clear, nuclear confined speckled pattern. It reacts also specifically with 5-bromouridine (BrU).
适用于: IHC-P, ICC/IF, Flow Cyt (Intra)more details
与反应: Species independent
Chemical/ Small Molecule corresponding to BrdU.
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Liquid
Shipped at 4°C. Store at +4°C. Do Not Freeze.
pH: 7.40
Preservative: 0.097% Sodium azide
Constituent: PBS
Protein A purified
>95 % (by PAGE).
单克隆
MoBu-1
IgG1
Abpromise™承诺保证使用ab8039于以下的经测试应用
“应用说明”部分 下显示的仅为推荐的起始稀释度;实际最佳的稀释度/浓度应由使用者检定。
应用 | Ab评论 | 说明 |
---|---|---|
IHC-P | Use at an assay dependent concentration. | |
ICC/IF | Use a concentration of 2 µg/ml. | |
Flow Cyt (Intra) | Use a concentration of 1 - 2 µg/ml. ab170190 - Mouse monoclonal IgG1, is suitable for use as an isotype control with this antibody. |
Bromodeoxyuridine antibody
BUdr antibody
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-BrdU antibody [MoBu-1] (ab8039)
Immunohistochemical analysis of parafin-embedded bromodeoxyuridine-labelled chick embryo cells with (MoBu-1) 5-bromodeoxyuridine
Immunocytochemistry/ Immunofluorescence - Anti-BrdU antibody [MoBu-1] (ab8039)
ICC/IF image of ab8039 stained HeLa cells, both BrdU treated (left image) and normal cells (right image). The cells were 100% methanol fixed (5 min) and then subjected to acid hydrolysis using 2M HCL in 0.1% PBS-Tween for 30 minutes at room temperature to denature the DNA. They were then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab8039, 10µg/ml) overnight at +4°C. The secondary antibody (green) was ab96879, DyLight® 488 goat anti-mouse IgG (H+L) used at a 1/250 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM. Positive staining can be seen in the BrdU treated cells, but not in the normal cells, demonstrating specificity for BrdU.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-BrdU antibody [MoBu-1] (ab8039)
IHC image of ab8039 staining, both in normal and BrdU treated rat liver formalin fixed paraffin embedded tissue sections, performed on a Leica Bond<sup>tm< sup>="" system="" using="" the="" standard="" protocol="" f.="" section="" was="" pre-treated="" heat="" mediated="" antigen="" retrieval="" with="" sodium="" citrate="" buffer="" (ph6,="" epitope="" solution="" 1)="" for="" 20="" mins.="" then="" incubated="" ab8039,="" 5µg="" ml,="" 15="" mins="" at="" room="" temperature="" and="" detected="" an="" hrp="" conjugated="" compact="" polymer="" system.="" dab="" used="" as="" chromogen.="" counterstained="" haematoxylin="" mounted="" dpx.
For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.
Flow Cytometry (Intracellular) - Anti-BrdU antibody [MoBu-1] (ab8039)
Intracellular Flow Cytometry analysis of CEM (human acute lymphoblastic leukemia) cells labelling BrdU with ab8039 at 1µg/mL. Goat anti-mouse IgG was used as the secondary antibody.The individual cell cycle phases (S, G1, G2/M-phase) are indicated on the figure.