Anti-Cullin 4B antibody
cat.: ER2001-65
Product Type: Rabbit polyclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IHC, FC
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), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1 mg/mL.
Purification: Peptide affinity purified.
Molecular weight: Predicted band size: 103/84 kDa.
Isotype: IgG
Immunogen: Synthetic peptide within human Cullin 4B aa 850-913.
Positive control: HUVEC cell lysates, rat cerebellum tissue, human colon tissue, mouse testis tissue, Daudi.
Subcellular location: Nucleus.
Recommended Dilutions:
  WB
  IHC
  FC

1:500-1:1,000
1:200-1:1,000
1:50-1:100
Uniprot #: SwissProt: Q13620 Human | A2A432 Mouse
Alternative names: CUL 4B CUL-4B CUL4B CUL4B_HUMAN Cullin-4B DKFZp686F1470 KIAA0695 MRXHF2 MRXSC SFM2
Images
ER2001-65_1.jpg Fig1: Western blot analysis of Cullin 4B on HUVEC cell lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (ER2001-65, 1/500) was used 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.
ER2001-65_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded rat cerebellum tissue using anti-Cullin 4B 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 (ER2001-65, 1/1000) 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.
ER2001-65_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded human colon tissue using anti-Cullin 4B 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 (ER2001-65, 1/500) 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.
ER2001-65_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded mouse testis tissue using anti-Cullin 4B 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 (ER2001-65, 1/1000) 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.
ER2001-65_5.jpg Fig5: Flow cytometric analysis of Cullin 4B was done on Daudi cells. The cells were fixed, permeabilized and stained with the primary antibody (ER2001-65, 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated Goat anti-Rabbit IgG Secondary antibody at 1/1000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.