Anti-CD44抗体[156-3C11]
参阅全部 CD44 一抗
小鼠单克隆抗体[156-3C11] to CD44
Mouse
适用于: ICC/IF, IHC-P, Flow Cytmore details
与反应: Human, Baboon
Tissue, cells or virus corresponding to Human CD44. Stimulated human leukocytes
Tonsil, HeLa cell line
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Liquid
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Store at -20°C or -80°C. Avoid freeze / thaw cycle.
pH: 7.3
Preservative: 0.05% Sodium azide
Constituent: 1% BSA
Protein A purified
单克隆
156-3C11
IgG2a
Abpromise™承诺保证使用ab16728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 | 1/100. | |
IHC-P | (2) | 1/25 - 1/75. Perform heat mediated antigen retrieval before commencing with IHC staining protocol. |
Flow Cyt | 1/1000. ab170191 - Mouse monoclonal IgG2a, is suitable for use as an isotype control with this antibody. |
Entrez Gene: 101008690 Baboon
Entrez Gene: 960 Human
Omim: 107269 Human
SwissProt: P16070 Human
Unigene: 502328 Human
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Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD44 antibody [156-3C11] (ab16728)This image is courtesy of an anonymous Abreview
ab16728 at 1/50 dilution staining baboon skin tissue sections by Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections). The sections were fixed with formaldehyde and blocked with a 1% Hydrogen peroxide / Methanol solution prior to incubation with the antibody for 1 hour. A biotinylated swine anti-goat, mouse, rabbit antibody was used as the secondary.
Flow Cytometry - Anti-CD44 antibody [156-3C11] (ab16728)
Human peripheral blood lymphocytes stained with ab16728 (red). Human whole blood was processed using a modified protocol based on Chow et al, 2005 (PMID: 16080188). In brief, human whole blood was fixed in 4% formaldehyde (methanol-free) for 10 min at 22°C. Red blood cells were then lyzed by the addition of Triton X-100 (final concentration - 0.1%) for 15 min at 37°C. For experimentation, cells were treated with 50% methanol (-20°C) for 15 min at 4°C. Cells were then incubated with the antibody (ab16728, 1/1000 dilution) for 30 min at 4°C. The secondary antibody used was Alexa Fluor® 488 goat anti-mouse IgG (H&L) (ab150113) at 1/2000 dilution for 30 min at 4°C. Acquisition of >30,000 total events were collected using a 20mW Argon ion laser (488nm) and 525/30 bandpass filter. Gating strategy - peripheral blood lymphocytes.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD44 antibody [156-3C11] (ab16728)
ab16728 staining human tonsil by IHC-P.
Immunocytochemistry/ Immunofluorescence - Anti-CD44 antibody [156-3C11] (ab16728)
ICC/IF image of ab16728 stained HeLa 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 (ab16728, 1/100 dilution) 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.