Caspase-10 Recombinant Rabbit Monoclonal Antibody [JJ0890]
cat.: ET1701-53
| Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
|---|---|
| Species reactivity: | Human |
| Applications: | WB, IHC-P, FC, IP, IF-Cell |
| Clonality: | Monoclonal |
| Clone number: | JJ0890 |
| Form: | Liquid |
| Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles. |
| Storage buffer: | 1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide. |
| Concentration: | 1ug/ul |
| Purification: | Protein A affinity purified. |
| Molecular weight: | Predicted band size: 59 kDa |
| Isotype: | IgG |
| Immunogen: | Recombinant protein within Human Caspase-10 aa 254-452 / 521. |
| Positive control: | Jurkat cell lysate, K-562 cell lysate, HepG2 cell lysate, A431 cell lysate, Jurkat, human kidney tissue, human liver tissue. |
| Subcellular location: | Cytosol. |
| Recommended Dilutions:
WB FC IHC-P IP IF-Cell |
1:1,000-1:2,000 1:1,000 1:50-1:200 1-2μg/sample 1:100 |
| Uniprot #: | SwissProt: Q92851 Human |
| Alternative names: | Caspase10 ALPS2 Apoptotic protease Mch-4 CASP 10 CASP-10 CASP10 CASPA_HUMAN Caspase 10 apoptosis related cysteine peptidase Caspase-10 subunit p12 FADD like ICE2 Fas associated death domain protein FAS-associated death domain protein interleukin-1B-converting enzyme 2 FLICE 2 FLICE2 ICE like apoptotic protease 4 ICE-like apoptotic protease 4 Interleukin 1B converting enzyme 2 MCH 4 |
Images
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Fig1:
Western blot analysis of Caspase-10 on different lysates with Rabbit anti-Caspase-10 antibody (ET1701-53) at 1/2,000 dilution. Lane 1: Jurkat cell lysate Lane 2: K-562 cell lysate Lane 3: HepG2 cell lysate Lane 4: A431 cell lysate Lysates/proteins at 20 µg/Lane. Predicted band size: 59 kDa Observed band size: 59/58 kDa Exposure time: 2 minutes; ECL: K1801; 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 (ET1701-53) at 1/2,000 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. |
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Fig2:
Immunocytochemistry analysis of Jurkat cells labeling Caspase-10 with Rabbit anti-Caspase-10 antibody (ET1701-53) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 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-10 antibody (ET1701-53) 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 (HA601187, 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. |
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Fig3:
Immunohistochemical analysis of paraffin-embedded human kidney tissue with Rabbit anti-Caspase-10 antibody (ET1701-53) at 1/200 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1701-53) at 1/200 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX. |
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Fig4:
Immunohistochemical analysis of paraffin-embedded human liver tissue with Rabbit anti-Caspase-10 antibody (ET1701-53) at 1/50 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1701-53) at 1/50 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX. |
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Fig5:
Flow cytometric analysis of Jurkat cells labeling Caspase-10. Cells were fixed and permeabilized. Then stained with the primary antibody (ET1701-53, 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). |
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Fig6:
Caspase-10 was immunoprecipitated from 0.2 mg K-562 cell lysate with ET1701-53 at 2 µg/10 µl beads. Western blot was performed from the immunoprecipitate using ET1701-53 at 1/2,000 dilution. HRP Conjugated Anti-Rabbit IgG for IP secondary antibody at 1/5,000 dilution was used for 1 hour at room temperature. Lane 1: K-562 cell lysate (input) Lane 2: ET1701-53 IP in K-562 cell lysate Lane 3: Rabbit IgG instead of ET1701-53 in K-562 cell lysate Blocking/Dilution buffer: 5% NFDM/TBST Exposure time: 1 minute 7 seconds; ECL: K1802 |
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