ASC antibody | knockout validation | AdipoGen Life Sciences AG25B-006
DOI
//dx.doi.org/10.13070/ko.en.6.1927
Date
2016-12-18

This is a knockout-validated antibody summary, based on the publication "ASC filament formation serves as a signal amplification mechanism for inflammasomes", as cited below [1]. Labome curates formal publications to compile a list of antibodies with unambiguous specificity within Validated Antibody Database (VAD).

ASC antibody | knockout validation | AdipoGen Life Sciences AG25B-006 figure 1
Figure 1. From Supplementary Figure S1 in From [1]. Western blot of lysates of wild-type and ASC knockout BMDMs probed with anti-ASC antibody. Actin serves as a loading control.
Antibody information

Rabbit polyclonal

Company: Adipogen Life Sciences

Antibody: ASC

Catalog number: AG-25B-006

Summary: Rabbit polyclonal antibody raised against a synthetic peptide corresponding to sequence in the N-terminal region of human ASC. Supplier recommended for WB, IP, ICC and IHC. Antibody is epitope affinity-purified. Reacts with mouse and human ASC.

Validation Method

Western blot

Sample

Lysates of wild-type and ASC -/- immortalised bone marrow derived macrophages (BMDMs).

Blocking agent

TBS-T containing 5% milk powder.

Primary incubation

Anti-ASC antibody diluted 1:1000 in blocking buffer.

Secondary incubation

HRP-conjugated secondary antibody diluted 1:5000 in blocking buffer.

Disclaimer

If the antibody described in this summary is a polyclonal antibody, since polyclonal antibodies are of limited quantity, please inquire the supplier whether any current polyclonal antibody with the same catalog number is exactly the same as the one described in this summary. Sometimes, different bleeds or different animals are used, usually with a different lot number. In such cases, the result in this summary may not apply to the new antibody with the same catalog number.

References
  1. Dick M, Sborgi L, Rühl S, Hiller S, Broz P. ASC filament formation serves as a signal amplification mechanism for inflammasomes. Nat Commun. 2016;7:11929 pubmed publisher