• Tel: 858.663.9055
  • separatorEmail: info@nsjbio.com
  • Tel: 858.663.9055
  • Email: info@nsjbio.com
banner Search results for Cortactin

Cortactin Antibody

Catalog No : RQ4531
Applications : WB, IHC-P, IF/ICC, FACS
Reactivity : Human, Mouse, Rat
Format : Antigen affinity purified
Western blot testing of human 1) A431, 2) U-87 MG, 3) A549, 4) PC-3 and 5) HeLa lysate with Cortactin antibody at 0.5ug/ml. Predicted molecular weight ~61 kDa but routinely observed at ~80 kDa.
›
img img img img img img img img img img

Cortactin Antibody

Catalog No : R36346
Applications : WB, ELISA (peptide)
Reactivity : Human, Mouse
Pred. Reactivity :Rat, Dog, Cow
Format : Antigen affinity purified
Western blot testing of mouse brain lysate with Cortactin antibody at 0.01ug/ml. Molecular weight: routinely observed at ~80kDa.
›
img img

Cortactin Antibody (clone 401CT8.6.3)

Catalog No : F53608
Applications : WB, ELISA
Reactivity : Human
Format : Ascites
Cortactin antibody western blot analysis in MDA-MB231 lysate. Molecular weight: routinely observed at ~80kDa.
img

SHANK1 Antibody / SH3 and multiple ankyrin repeat domains protein 1

Catalog No : FY12464
Applications : WB, ICC/IF, FACS, ELISA
Reactivity : Human, Mouse, Rat
Format : Lyophilized
Immunofluorescent staining of SHANK1 using anti-SHANK1 antibody (green). SHANK1 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 ug/ml rabbit anti-SHANK1 antibody overnight at 4oC. DyLight 488 Conjugated Goat Anti-Rabbit IgG was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37oC. The section was counterstained with DAPI nuclear stain (blue). Visualize using a fluorescence microscope and filter sets appropriate for the label used.
›
img img img

SHANK2 Antibody / SH3 and multiple ankyrin repeat domains protein 2

Catalog No : FY12955
Applications : WB, FACS, ELISA
Reactivity : Human, Mouse, Rat
Format : Lyophilized
Flow Cytometry analysis of Caco-2 cells using anti-SHANK2 antibody. Overlay histogram showing Caco-2 cells stained with (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SHANK2 antibody (1 ug/million cells) for 30 min at 20oC. DyLight 488 conjugated goat anti-rabbit IgG (5-10 ug/million cells) was used as secondary antibody for 30 minutes at 20oC. Isotype control antibody (Green line) was rabbit IgG (1 ug/million cells) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
›
img img