Ankyron CALX_HUMAN Clone AY40204

HeLa cells were stained using 10 µg V5-tagged Ankyron and anti-V5 antibody conjugated with APC (red) in Permeabilization Staining Buffer (RPMI 1640 + 10 % human serum + 0.5 % saponin, counterstaining nuclei with DAPI (blue). Image captured by epifluorescence microscopy.

HUVEC were stained using 1.4 µg V5-tagged Ankyron and anti-V5 antibody conjugated with APC (red) in Permeabilisation Staining Buffer (RPMI 1640 + 10 % human serum + 0.5 % saponin), counterstaining nuclei with DAPI (blue) and F-actin with Phalloidin. Inset: negative control of anti-V5 APC antibody alone and F-actin staining.

Immunohistochemical analysis of paraffin-embedded human liver using 10 μg/ml V5-tagged Ankyron and anti-V5 HRP (1 in 500), detecting with DAB (brown) and counterstaining nuclei with haematoxylin (blue-purple). Heat-mediated antigen retrieval with Leica EDTA buffer (pH9), 40 min.

Flow cytometric analysis of HeLa cells following permeabilisation then incubation with pre-conjugated Ankyron (0.4 μg) and anti-V5 APC (red). Negative control, anti-V5 APC only (grey).

Colorimetric western blot analysis of purified Fc-tagged target protein (100 - 10 ng) and cell lysates prepared from either HeLa or HCT116 cells, using 1 µg/ml V5-tagged Ankyron premixed with anti-V5-HRP antibody.

Colorimetric western blot analysis of purified target protein (1µg - 10 ng) and lysates from HeLa cells using 1 µg/ml V5-tagged Ankyron preconjugated with anti-V5-HRP (1 in 500).

Binding assay determination of the signal to noise ratio (SNR) of V5-labeled Ankyrons® AY40204 binding to 0.5 picomoles of immobilised CALX_HUMAN, over a background (BG) of non-cognate target protein. The Ankyron was pre-conjugated with the ProImmune Anti-V5 HRP label reagent before detection with a chemiluminescence substrate.