ATG16L antibody | knockout validation | MBL PM040
DOI
//dx.doi.org/10.13070/ko.en.6.1789
Date
2016-11-08

This is a knockout-validated antibody summary, based on the publication "The Parkinson's disease-associated genes ATP13A2 and SYT11 regulate autophagy via a common pathway", as cited below [1]. Labome curates formal publications to compile a list of antibodies with unambiguous specificity within Validated Antibody Database (VAD).

ATG16L antibody | knockout validation | MBL PM040 figure 1
Figure 1. Western blot of lysates from wild-type and ATG16L -/- HeLa cells probed with anti-ATG16L antibody. Actin serves as a loading control. From [1].
Antibody information

Rabbit polyclonal

Company: MBL

Antibody: ATG16L

Catalog number: PM040

Summary: Rabbit polyclonal antibody raised against recombinant human ATG16L1 TV2, residues 85-588.

Antibody is affinity purified.

Supplier recommended for ICC, IP and WB.

Reacts with hamster, human, mouse and rat ATG16L.

Validation Method

Western blot

Sample

Wild-type and ATG16L -/- Hela cell lysates.

Blocking agent

PBS containing 5% milk powder and 0.2% Tween 20.

Primary incubation

1:1000 overnight at 4oC.

Secondary incubation

1:2000 with HRP-conjugated anti-rabbit IgG (NA934V; GE Healthcare) for 1 hour at room temperature.

Detection

ECL Reagent (Pierce).

Image J software for data capture and densitometry.

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. Bento C, Ashkenazi A, Jimenez-Sanchez M, Rubinsztein D. The Parkinson's disease-associated genes ATP13A2 and SYT11 regulate autophagy via a common pathway. Nat Commun. 2016;7:11803 pubmed publisher