FAB1A Rabbit Polyclonal Antibody
cat.: HA500403
Product Type: Rabbit polyclonal IgG, primary antibodies
Species reactivity: Arabidopsis thaliana
Applications: IF-Tissue, IHC-P
Clonality: Polyclonal
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*TBS (pH7.4), 1% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Immunogen affinity purified.
Molecular weight: 196 kDa
Isotype: IgG
Immunogen: Synthetic peptide within Arabidopsis thaliana FAB1A aa 100-200 / 1757.
Positive control: A. thaliana tissue.
Subcellular location: Endosome membrane.
Recommended Dilutions:
  IF-Tissue
  IHC-P

1:50-1:100
1:50-1:200
Uniprot #: SwissProt: Q0WUR5 ARATH
Alternative names: 1-phosphatidylinositol-3-phosphate 5-kinase FAB1A Phosphatidylinositol 3-phosphate 5-kinase FYVE finger-containing phosphoinositide kinase PIKfyve Phosphatidylinositol 3-phosphate 5-kinase type III PIPkin-III Type III PIP kinase Protein FORMS APLOID AND BINUCLEATE CELLS 1A FAB1A At4g33240 F4I10.170
Images
HA500403_1.jpg Fig1: Immunofluorescence staining of paraffin- embedded A. thaliana using anti-FAB1A rabbit polyclonal antibody.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 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with HA500403 at 1/100 dilution for 10 hours at 4℃ and detected using Alexa Fluor® 488 conjugate-Goat anti-Rabbit IgG (H+L) Secondary Antibody at a dilution of 1:500 for 1 hour at room temperature.
HA500403_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded A. thaliana tissue using anti-FAB1A antibody. 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 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA500403, 1/50) for 30 minutes 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”.