WDR68 Recombinant Rabbit Monoclonal Antibody [JE61-64]
cat.: HA720062
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IHC-P
Clonality: Monoclonal
Clone number: JE61-64
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: 39 kDa
Isotype: IgG
Immunogen: Synthetic peptide within human WDR68 aa 199-248/342.
Positive control: Hela cell lysate, 293 cell lysate, mouse lung tissue lysate, SH-SY5Y cell lysate, human prostate tissue, mouse brain tissue, rat epididymis tissue.
Subcellular location: Nucleus, Cytoplasm.
Recommended Dilutions:
  WB
  IHC-P

1:500-1:2,000
1:50-1:200
Uniprot #: SwissProt: P61962 Human | P61963 Mouse
Entrez Gene: 303602 Rat
Alternative names: AN11 Dcaf7 DCAF7_HUMAN DDB1- and CUL4-associated factor 7 HAN11 Human anthocyanin Petunia Seven WD repeat protein of the AN11 family 1 SWAN 1 WD repeat domain 68 WD repeat protein An11 homolog WD repeat-containing protein 68 WD repeat-containing protein An11 homolog WDR68
Images
HA720062_1.jpg Fig1: Western blot analysis of WDR68 on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA720062, 1/500) was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:200,000 dilution was used for 1 hour at room temperature.
Positive control:
Lane 1: Hela cell lysate
Lane 2: 293 cell lysate
Lane 3: Mouse lung tissue lysate
Lane 4: SH-SY5Y cell lysate
HA720062_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human prostate tissue using anti-WDR68 antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) 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 (HA720062, 1/200) 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.
HA720062_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded mouse brain tissue using anti-WDR68 antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) 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 (HA720062, 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”.