NSD3 Recombinant Rabbit Monoclonal Antibody [SN07-11]
cat.: ET1611-39
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, FC, IHC-P
Clonality: Monoclonal
Clone number: SN07-11
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. 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: Predicted band size: 162 kDa
Isotype: IgG
Immunogen: Synthetic peptide within Human NSD3 aa 1-50 / 1,437.
Positive control: MCF-7 cell lysate, 293T cell lysate, human small intestine tissue, Hela, human lymph nodes tissue.
Subcellular location: Nucleus, Chromosome.
Recommended Dilutions:
  WB
  FC
  IHC-P

1:1,000-1:2,000
1:50-1:100
1:50-1:400
Uniprot #: SwissProt: Q9BZ95 Human | Q6P2L6 Mouse | D3ZK47
Alternative names: DKFZp667H044 FLJ20353 Histone lysine N methyltransferase NSD3 Histone-lysine N-methyltransferase NSD3 MGC126766 MGC142029 NSD 3 NSD3_HUMAN Nuclear set domain containing 3 Nuclear SET domain containing protein 3 Nuclear SET domain-containing protein 3 pp14328 Protein whistle Whistle WHSC1 like protein 1 WHSC1-like 1 isoform 9 with methyltransferase activity to lysine WHSC1-like protein 1 WHSC1L1 WHSC1L1 protein Wolf Hirschhorn syndrome candidate 1 like 1 Wolf-Hirschhorn syndrome candidate 1-like protein 1
Images
ET1611-39_1.jpg Fig1: Western blot analysis of NSD3 on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (ET1611-39, 1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:40,000 dilution was used for 1 hour at room temperature.
Positive control:
Lane 1: MCF-7 cell lysate
Lane 2: 293T cell lysate
ET1611-39_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human small intestine tissue using anti-NSD3 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 primary antibody (ET1611-39, 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.
ET1611-39_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded human lymph nodes tissue with Rabbit anti-NSD3 antibody (ET1611-39) at 1/400 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 (ET1611-39) at 1/400 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.
ET1611-39_4.jpg Fig4: Flow cytometric analysis of NSD3 was done on Hela cells. The cells were fixed, permeabilized and stained with the primary antibody (ET1611-39, 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”.