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anti-Caspase-1 (p10) (mouse), mAb (Casper-2)

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AG-20B-0044-C100 100 µg $280.00
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Additional Information

Product Data
Synonyms Interleukin-1β Convertase; IL-1BC; Interleukin-1β-converting Enzyme; ICE
Properties
Clone Casper-2
Isotype Mouse IgG2a
Source/Host Purified from concentrated hybridoma tissue culture supernatant.
Immunogen/Antigen Recombinant mouse caspase-1.
Application Western Blot (see online protocol): (1μg/ml) (no need to precipitate the cell supernatant for the detection of caspase-1 (mouse) upon inflammasome activation)
Crossreactivity Mouse
Specificity Recognizes endogenous full-length and activated (p10 fragment) mouse caspase-1.
Purity ≥95% (SDS-PAGE)
Purity Detail Protein G-affinity purified.
Concentration 1mg/ml
Formulation Liquid. In PBS containing 10% glycerol and 0.02% sodium azide.
Product Type Monoclonal Antibody
Shipping and Handling
Shipping BLUE ICE
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice After opening, prepare aliquots and store at -20°C. Avoid freeze/thaw cycles.
Use/Stability Stable for at least 1 year after receipt when stored at -20°C.
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Product Description

Caspase-1 is the best-described inflammatory caspase. It processes the cytokines interleukin-1β (IL-1β) and IL-18 and induces pyroptotic cell death. Caspase-1 is activated by multiprotein complexes called inflammasomes in response to numerous stimuli that are detected through distinct inflammasomes. NLRC4 responds to cytosolic flagellin, murine NLRP1b responds to anthrax lethal toxin, AIM2 responds to cytosolic DNA and NLRP3 responds to a variety of agonists including crystals.
Mouse Caspase-1 (p10) is detected by immunoblotting using anti-Caspase-1 (p10) (mouse), mAb (Casper-2) (Prod. No AG-20B-0044). <b>Method:</b> Caspase-1 was analyzed by Western blot in supernatants of differentiated bone marrow-derived dendritic cells (BMDCs) from wild-type and caspase-1<sup>-/-</sup> mice activated or not by 5 &mu;M Nigericin for 30 min (Prod. No. AG-CN2-0020). Supernatants (30&mu;l) were separated by SDS-PAGE under reducing conditions, transferred to nitrocellulose and incubated with anti-Caspase-1 (p10) (mouse), mAb (Casper-2) (1&mu;g /ml). Proteins were visualized by a chemiluminescence detection system.
Mouse Caspase-1 (p10) is detected by immunoblotting using anti-Caspase-1 (p10) (mouse), mAb (Casper-2) (Prod. No AG-20B-0044). Method: Caspase-1 was analyzed by Western blot in supernatants of differentiated bone marrow-derived dendritic cells (BMDCs) from wild-type and caspase-1-/- mice activated or not by 5 μM Nigericin for 30 min (Prod. No. AG-CN2-0020). Supernatants (30μl) were separated by SDS-PAGE under reducing conditions, transferred to nitrocellulose and incubated with anti-Caspase-1 (p10) (mouse), mAb (Casper-2) (1μg /ml). Proteins were visualized by a chemiluminescence detection system.
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