Anti-Cdc27抗体[AF3.1]
参阅全部 Cdc27 一抗
小鼠单克隆抗体[AF3.1] to Cdc27
Mouse
适用于: WB, IHC-P, Flow Cytmore details
与反应: Mouse, Human
Synthetic peptide conjugated to KLH, corresponding to amino acids 814-823 of Human Cdc27.
HeLa cell nuclear extract.
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Liquid
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
Preservative: 0.02% Sodium azide
Constituent: 99.98% PBS
浓度
100 µg 浓度为 0.5 mg/ml
100 µg 浓度为 0.5 mg/ml
Protein A purified
单克隆
AF3.1
IgG2b
Abpromise™承诺保证使用ab10538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 |
---|---|---|
WB | (1) | Use a concentration of 1 - 2 µg/ml. Detects a band of approximately 80 kDa (predicted molecular weight: 92 kDa). |
IHC-P | Use at an assay dependent concentration. | |
Flow Cyt | Use 1µg for 106 cells. ab170192 - Mouse monoclonal IgG2b, is suitable for use as an isotype control with this antibody. |
Entrez Gene: 996 Human
Entrez Gene: 217232 Mouse
Omim: 116946 Human
SwissProt: P30260 Human
SwissProt: A2A6Q5 Mouse
Unigene: 463295 Human
Unigene: 89845 Mouse
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Western blot - Anti-Cdc27 antibody [AF3.1] (ab10538)
All lanes : Anti-Cdc27 antibody [AF3.1] (ab10538)
Lane 1 : HeLa cell lysate
Lane 2 : 293 cell lysate
Lane 3 : Mouse myeloid cell lysate
Predicted band size: 92 kDa
Observed band size: 80 kDawhy is the actual band size different from the predicted?
We have no more information on how this image was prepared by the academic who produced the antibody.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Cdc27 antibody [AF3.1] (ab10538)
IHC image of ab10538 staining in human cervical carcinoma formalin fixed paraffin embedded tissue section, performed on a Leica BondTM system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20 mins. The section was then incubated with ab10538, 1µg/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with 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 - Anti-Cdc27 antibody [AF3.1] (ab10538)
Overlay histogram showing K562 cells stained with ab10538 (red line). The cells were fixed with 4% paraformaldehyde (10 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab10538, 1µg/1x106 cells) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22ºC. Isotype control antibody (black line) was mouse IgG2b [PLPV219] (ab91366, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in K562 cells fixed with 80% methanol (5 min)/permeabilized with 0.1% PBS-Tween for 20 min used under the same conditions.
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