Anti-CD59抗体[MEM-43/5]
参阅全部 CD59 一抗
小鼠单克隆抗体[MEM-43/5] to CD59
Mouse
CD59 antigen (human). MEM-43/5 reacts with well defined epitope (around L33) and does not compete with MEM-43 and many other CD59 antibodies
适用于: ICC/IF, IP, IHC-P, Flow Cyt, WBmore details
与反应: Mouse, Human
Tissue, cells or virus corresponding to Human CD59. Thymocytes and T lymphocytes
The antibody MEM-43/5 reacts with well defined epitope around L33 (see Bodian et al)
Flow cyt: blood Jeg3 cell line IF/ICC
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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
Purity >95% by SDS-PAGE.
单克隆
MEM-43/5
unknown
IgG2b
unknown
Abpromise™承诺保证使用ab9183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 |
---|---|---|
ICC/IF | Use a concentration of 5 µg/ml. | |
IP | Use at an assay dependent concentration. | |
IHC-P | (1) | Use a concentration of 5 µg/ml. |
Flow Cyt | Use a concentration of 0.5 - 4 µg/ml. ab170192 - Mouse monoclonal IgG2b, is suitable for use as an isotype control with this antibody. | |
WB | Use at an assay dependent concentration. Predicted molecular weight: 14 kDa. CD59 is GPI-anchored, so we recommend to use a laurylmatoside based lysis buffer or triton base buffer (see Bodian et al; 1% Triton X-100, 1 µg/ml leupeptin, 1 µg/ml pepstatin A and 1 mM phenlymethylsulphonyl fluoride in PBS), not NP40. Read More |
Entrez Gene: 966 Human
Entrez Gene: 12509 Mouse
Omim: 107271 Human
SwissProt: P13987 Human
SwissProt: O55186 Mouse
Unigene: 278573 Human
Unigene: 709466 Human
Unigene: 710641 Human
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CD59_HUMAN antibody
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MAC-inhibitory protein antibody
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Membrane attack complex (MAC) inhibition factor antibody
Membrane attack complex inhibition factor antibody
Membrane inhibitor of reactive lysis antibody
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MSK21 antibody
p18 20 antibody
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Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD59 antibody [MEM-43/5] (ab9183)
Immunohistochemistry parafin embedded sections staining of huam skin tissue using ab9183.
Flow Cytometry - Anti-CD59 antibody [MEM-43/5] (ab9183)
Flow cytometric analysis of Human Peripheral Blood cells labelling CD59 with ab9183 at 0.6 ug/ml showing separation of human neutrophil granulocytes (red-filled) from human CD59 negative blood debris (black-dashed).
Immunocytochemistry/ Immunofluorescence - Anti-CD59 antibody [MEM-43/5] (ab9183)
ICC/IF image of ab9183 stained Jeg3 cells. The cells were 4% formaldehyde fixed (10 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 (ab9183, 5µg/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.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD59 antibody [MEM-43/5] (ab9183)
IHC image of ab9183 staining CD59 in Human normal placenta 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 EDTA (pH9, epitope retrieval solution 2) for 20 mins. The section was then incubated with ab9183, 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.
Flow Cytometry - Anti-CD59 antibody [MEM-43/5] (ab9183)
Overlay histogram showing Jurkat cells stained with ab9183 (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 (ab9183, 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 Jurkat cells fixed with 80% methanol (5 min)/permeabilized with 0.1% PBS-Tween for 20 min used under the same conditions.