SEL1L Rabbit Polyclonal Antibody
cat.: ER1803-69
Product Type: Rabbit polyclonal IgG, primary antibodies
Species reactivity: Zebrafish
Applications: WB, 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*PBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Immunogen affinity purified.
Molecular weight: Predicted band size: 86 kDa
Isotype: IgG
Immunogen: Recombinant protein within zebrafish SEL1L aa 109-281 / 776.
Positive control: Zebrafish lysate, Zebrafish.
Subcellular location: Cytoplasm.
Recommended Dilutions:
  WB
  IF-Tissue
  IHC-P

1:500
1:50-1:200
1:200
Uniprot #: SwissProt: Q5RIK6 Zebrafish
Alternative names: IBD2 PRO1063 Protein sel-1 homolog 1 SE1L1_HUMAN Sel 1 like protein Sel 1 suppressor of lin 12 like Sel-1L SEL1 LIKE Sel1l SEL1LIKE Suppressor of lin-12-like protein 1 TSA305 UNQ128 UNQ128/PRO1063
Images
ER1803-69_1.jpg Fig1: Western blot analysis of SeL1L on Zebrafish lysate. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody was used at a 1/500 dilution in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:5,000 dilution was used for 1 hour at room temperature.
ER1803-69_2.jpg Fig2: Immunofluorescence staining of paraffin-embedded zebrafish using anti-SEL1L 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 the antibody (ER1803-69) at 1/50 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.
ER1803-69_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded zebrafish tissue using anti-SeL1L antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) 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 antibody (ER1803-69) at 1/100 dilution, for 30 minutes at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chrogen. Counter stained with hematoxylin and mounted with DPX.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.