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Anti caspase 3 antibody

Manufactured by BD
Sourced in United States

Anti-caspase-3 antibody is a laboratory reagent used in research applications. It is a protein that binds specifically to the caspase-3 enzyme, which plays a role in the process of apoptosis, or programmed cell death. The antibody can be used to detect and quantify the presence of caspase-3 in biological samples.

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3 protocols using anti caspase 3 antibody

1

Caspase-3 Activation by Measles Virus

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Example 3

Caspase-3 Activation after MV or MV-deltaC Infection

The caspase-3 activation was analysed both in tumour cells infected with unmodified MV and MV-deltaC (FIG. 7B). A panel of two epithelioid mesothelioma cell lines (Meso13 and Meso56), one melanoma cell line (M17) and one lung adenocarcinoma cell line (A549) were infected with unmodified MV or MV-deltaC, at a MOI of 1.0 for 2 hours, incubation at 37° C. Control cell lines were not infected with MV or MV-deltaC. Virus infected (MV or MV-deltaC) and uninfected tumour cells were analysed by flow cytometry after staining with an anti-caspase-3 antibody (BD Biosciences) three days after infection.

Infection with MV-deltaC induced caspase-3 activation for the two different tested cell lines: 38.2% for Meso13 epithelioid mesothelioma cells, 30.2% for M17 melanoma cells, 21.8% for A549 lung adenocarcinoma cells and 8.4% for Meso56 epithelioid mesothelioma cells. On the contrary, this caspase-3 activation was not or partially observed after infection with unmodified MV. These results suggested that unmodified MV and MV-deltaC viruses could induce the tumour cell death according to two different pathways.

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2

Caspase-3 Activation by Oncolytic Viruses

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Example 3

Caspase-3 Activation After MV or MV-DeltaC Infection

The caspase-3 activation was analysed both in tumour cells infected with unmodified MV and MV-deltaC (FIG. 7B). A panel of two epithelioid mesothelioma cell lines (Meso13 and Meso56), one melanoma cell line (M17) and one lung adenocarcinoma cell line (A549) were infected with unmodified MV or MV-deltaC, at a MOI of 1.0 for 2 hours, incubation at 37° C. Control cell lines were not infected with MV or MV-deltaC. Virus infected (MV or MV-deltaC) and uninfected tumour cells were analysed by flow cytometry after staining with an anti-caspase-3 antibody (BD Biosciences) three days after infection.

Infection with MV-deltaC induced caspase-3 activation for the two different tested cell lines: 38.2% for Meso13 epithelioid mesothelioma cells, 30.2% for M17 melanoma cells, 21.8% for A549 lung adenocarcinoma cells and 8.4% for Meso56 epithelioid mesothelioma cells. On the contrary, this caspase-3 activation was not or partially observed after infection with unmodified MV. These results suggested that unmodified MV and MV-deltaC viruses could induce the tumour cell death according to two different pathways.

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3

Antibody-based Protein Expression Analysis

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Antibodies against SERCA1 (#12293) and SERCA2a (#4388) were purchased from Cell Signaling Technologies (Beverly, MA, USA). Anti-caspase-3 antibody (#67341A) was obtained from BD Pharmingen (San Diego, CA, USA). BA-F8 (type I MHC), SC-71 (type IIa MHC), and BF-F3 (type IIb MHC) were obtained from the Developmental Studies Hybridoma Bank (Iowa City, IA, USA). An antibody against SLN was a kind gift from Dr Muthu Periasamy (University of Central Florida). HRP-conjugated secondary antibodies (anti-rabbit IgG, horseradish peroxidase-linked F(ab′)2 fragment; #NA9340 V) were purchased from GE Healthcare. HRP-conjugated rabbit anti-goat IgG (H + L) antibody (#611620) was obtained from Invitrogen (Carlsbad, CA, USA).
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