Caspase-1 Recombinant Rabbit Monoclonal Antibody [SU40-07] - BSA and Azide free

This data was developed using ET1608-69, the same antibody clone in a different buffer formulation.
Western blot analysis of Caspase-1 on different lysates with Rabbit anti-Caspase-1 antibody (ET1608-69) at 1/100,000 dilution.

Lane 1: THP-1 cell lysate
Lane 2: HCT 116 cell lysate
Lane 3: HL-60 cell lysate
Lane 4: RAW264.7 cell lysate
Lane 5: Mouse spleen lysate
Lane 6: Rat spleen lysate

Lysates/proteins at 10 µg/Lane.

Predicted band size: 45 kDa
Observed band size: 45 kDa

Exposure time: 3 minutes;

4-20% SDS-PAGE gel.

Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (ET1608-69) at 1/100,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.

This data was developed using ET1608-69, the same antibody clone in a different buffer formulation.
Western blot analysis of Caspase-1 on U937 cell lysates with Rabbit anti-Caspase-1 antibody (ET1608-69) at 1/50,000 dilution.

Lysates/proteins at 10 µg/Lane.

Predicted band size: 45 kDa
Observed band size: 45 kDa

Exposure time: 1 minute;

10% SDS-PAGE gel.

Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (ET1608-69) at 1/50,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/100,000 dilution was used for 1 hour at room temperature.

This data was developed using ET1608-69, the same antibody clone in a different buffer formulation.
Immunocytochemistry analysis of HL-60 cells labeling Caspase-1 with Rabbit anti-Caspase-1 antibody (ET1608-69) at 1/100 dilution.

Cells were fixed in 80% precooled methanol for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-Caspase-1 antibody (ET1608-69) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.

Beta tubulin (M1305-2, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.

This data was developed using ET1608-69, the same antibody clone in a different buffer formulation.
Immunocytochemistry analysis of PC-12 cells labeling Caspase-1 with Rabbit anti-Caspase-1 antibody (ET1608-69) at 1/100 dilution.

Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-Caspase-1 antibody (ET1608-69) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.

Beta tubulin (M1305-2, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.

This data was developed using ET1608-69, the same antibody clone in a different buffer formulation.
Immunocytochemistry analysis of THP-1 cells labeling Caspase-1 with Rabbit anti-Caspase-1 antibody (ET1608-69) at 1/100 dilution.

Cells were fixed in 80% precooled methanol for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-Caspase-1 antibody (ET1608-69) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.

Beta tubulin (M1305-2, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.

This data was developed using ET1608-69, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of PC-12 cells labeling Caspase-1.

Cells were fixed and permeabilized. Then stained with the primary antibody (ET1608-69, 1/1,000) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).