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Cell Line: MCF7, SKBR3, MDA-MB-231, T47D cell lines (ATCC) Method of validaon: Mass Cytometry Primary Anbody: STJ97436 An-Survivin An- body Secondary Anbody 165 Ho-IgG goat an-mouse Diluon rao: Used at 4 µg/ml Result The anbody can be used for mass cytometry analysis of Survivin expression. The specificity of the anbody to Sur- vivin should be shown in an addional experiment.- J. Wagner, University of Zurich Treatment of materials: The cells were cultured to 70%-80% plang density. For cell detachment, they were washed with pre-warmed PBS (Gibco) and 1X TrypLETM (Thermo Fisher) was added for 5 min at 37°C. For cell fixaon, 1.6% paraformaldehyde (Thermo Fisher) was added for 10 minutes at room temperature. Then, the cells were pipeed off the plate and col- lected in cold full growth medium to quench the paraformaldehyde. The cells were spun down and aliquoted in PBS (Gibco) prior to storage at -80°C. Protocol: Fixed cells were washed once with 1x PBS / 0.05% bovine serum albumin / 2mM EDTA cell staining buffer (CSB) prior to staining with the anbody (STJ92356, 4 µg/ml) in CSB for 45 min at 22°C. The cells were washed three mes with CSB. Then, the secondary anbody, a goat an-mouse 165Ho-IgG (1 µg/ml), was applied in CSB for 45 min at 22°C. The cells were washed with CSB and ddH20 prior to mass cytometry acquision. Anbody Customer Review: STJ97436 An-Survivin Anbody Anbody Rang: Figure: Overlay histogram showing different mammary epithelial cell lines stained with STJ97436 and an-mouse 165 Ho-IgG (orange line) or an-mouse 165 Ho-IgG alone (blue line).

Antibody Customer Review for Anti-Survivin Monoclonal Antibody (STJ97436)

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Cell Line: MCF7, SKBR3, MDA-MB-231, T47D cell lines (ATCC)

Method of validation: Mass Cytometry

Primary Antibody: STJ97436 Anti-Survivin Anti-body

Secondary Antibody 165Ho-IgG goat anti-mouse

Dilution ratio: Used at 4 µg/ml

Result

“The antibody can be used for mass cytometry analysis of Survivin expression. The specificity of the antibody to Sur-vivin should be shown in an additional experiment.”- J. Wagner, University of Zurich

Treatment of materials:

The cells were cultured to 70%-80% plating density. For cell detachment, they were washed with pre-warmed PBS (Gibco) and 1X TrypLETM (Thermo Fisher) was added for 5 min at 37°C. For cell fixation, 1.6% paraformaldehyde (Thermo Fisher) was added for 10 minutes at room temperature. Then, the cells were pipetted off the plate and col-lected in cold full growth medium to quench the paraformaldehyde. The cells were spun down and aliquoted in PBS (Gibco) prior to storage at -80°C.

Protocol: Fixed cells were washed once with 1x PBS / 0.05% bovine serum albumin / 2mM EDTA cell staining buffer (CSB) prior to staining with the antibody (STJ92356, 4 µg/ml) in CSB for 45 min at 22°C. The cells were washed three times with CSB. Then, the secondary antibody, a goat anti-mouse 165Ho-IgG (1 µg/ml), was applied in CSB for 45 min at 22°C. The cells were washed with CSB and ddH20 prior to mass cytometry acquisition.

Antibody Customer Review: STJ97436 Anti-Survivin Antibody

Antibody Rating:

Figure: Overlay histogram showing different

mammary epithelial cell lines stained with

STJ97436 and anti-mouse 165Ho-IgG (orange

line) or anti-mouse 165Ho-IgG alone (blue

line).