ATG12 Rabbit Polyclonal Antibody
cat.: R1404-1
Product Type: Rabbit polyclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IHC-P
Clonality: Polyclonal
Form: Liquid
Storage condition: Shipped at 4℃. Store at +4℃ short term (1-2 weeks). It is recommended to aliquot into single-use upon delivery. Store at -20℃ long term.
Storage buffer: 1*PBS (pH7.4), 0.2% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Immunogen affinity purified.
Molecular weight: Predicted band size: 15 kDa
Isotype: IgG
Immunogen: Synthetic peptide within human ATG12 aa 96-138.
Positive control: Rat kidney lysates, rat pancreas tissue, rat testis tissue.
Subcellular location: Cytoplasm
Recommended Dilutions:
  WB
  IHC-P

1:500-1:1,000
1:1,000
Uniprot #: SwissProt: O94817 Human | Q9CQY1 Mouse | Q2TBJ5 Rat
Alternative names: APG12-like APG12L ATG12 ATG12 autophagy related 12 homolog (S. cerevisiae) ATG12 autophagy related 12 homolog ATG12_HUMAN Autophagy 12 Autophagy-related protein 12 FBR93 HAPG12 Ubiquitin-like protein ATG12
Images
R1404-1_1.jpg Fig1: Western blot analysis on rat kidney lysates using anti-ATG12 rabbit polyclonal antibodies.
R1404-1_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded rat pancreas tissue with Rabbit anti-ATG12 antibody (R1404-1) at 1/1,000 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 (R1404-1) at 1/1,000 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.
R1404-1_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded rat testis tissue with Rabbit anti-ATG12 antibody (R1404-1) at 1/1,000 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 (R1404-1) at 1/1,000 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.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.