Anti-Cytokeratin 8抗体[C-43]
参阅全部 Cytokeratin 8 一抗
小鼠单克隆抗体[C-43] to Cytokeratin 8
Mouse
This antibody recognises the 52.5kDa Cytokeratin 8.
适用于: WB, ICC/IF, IHC-P, Flow Cyt (Intra)more details
与反应: Human
预测可用于: Sheep, Rabbit, Cow, Pig不与反应: Mouse, Rat, Chicken, Hamster, Xenopus laevis
Tissue, cells or virus corresponding to Human Cytokeratin 8. Cytoskeleton preparation from HeLa human cervix carcinoma cell line
IHC-P: Human lung FFPE tissue sections. ICC/IF: HepG2 cells WB: HeLa cell lysate Flow Cyt (Intra): MCF7 cells
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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.
pH: 7.40
Preservative: 0.097% Sodium azide
Constituent: PBS
浓度
100 µg 浓度为 1 mg/ml
Protein A purified
Purified from tissue culture supernatant. Purity >95% by SDS-PAGE.
单克隆
C-43
IgG1
Abpromise™承诺保证使用ab2530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 | Use at an assay dependent concentration. Predicted molecular weight: 52.5 kDa. | |
ICC/IF | Use at an assay dependent concentration. | |
IHC-P | Use a concentration of 10 µg/ml. | |
Flow Cyt (Intra) | Use a concentration of 0.5 - 4 µg/ml. ab170190 - Mouse monoclonal IgG1, is suitable for use as an isotype control with this antibody. |
Entrez Gene: 3856 Human
Entrez Gene: 100348891 Rabbit
Entrez Gene: 101110495 Sheep
Omim: 148060 Human
SwissProt: P05787 Human
Unigene: 533782 Human
Unigene: 708445 Human
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Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Cytokeratin 8 antibody [C-43] (ab2530)
IHC image of ab2530 staining in human lung formalin fixed paraffin embedded tissue section, performed on a Leica Bond 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 ab2530, 5µg/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.
Immunocytochemistry/ Immunofluorescence - Anti-Cytokeratin 8 antibody [C-43] (ab2530)
ICC/IF image of ab2530 stained HepG2 cells. The cells were 100% methanol fixed (5 min) and 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 (ab2530, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-mouse IgG (H+L) used at a 1/1000 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.
Western blot - Anti-Cytokeratin 8 antibody [C-43] (ab2530)
Anti-Cytokeratin 8 antibody [C-43] (ab2530) at 2 µg/ml + HeLA cell lysate
Predicted band size: 52.5 kDa
Flow Cytometry (Intracellular) - Anti-Cytokeratin 8 antibody [C-43] (ab2530)
Overlay histogram showing MCF7 cells stained with ab2530 (red line). The cells were fixed with 4% paraformaldehyde (10 min) and then permeabilized with 0.1% PBS-Triton X-100 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 (ab2530, 0.1µg/1x106 cells) for 30 min at 22°C. The secondary antibody used was Alexa Fluor® 488 goat anti-mouse IgG (H+L) (ab150113) at 1/2000 dilution for 30 min at 22°C. Isotype control antibody (black line) was mouse IgG1 [ICIGG1] (ab91353, 1µg/1x106 cells) used under the same conditions. Unlabelled sample (blue line) was also used as a control. Acquisition of >5,000 events were collected using a 20mW Argon ion laser (488nm) and 525/30 bandpass filter. This antibody gave a positive signal in MCF7 cells fixed with 80% methanol (5 min)/permeabilized with 0.1% PBS-Triton X-100 for 20 min used under the same conditions.