HDAC9 Recombinant Rabbit Monoclonal Antibody [JU30-44]
cat.: ET1706-36
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human
Applications: WB, IF-Cell, IF-Tissue, IHC-P, IP
Clonality: Monoclonal
Clone number: JU30-44
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: 111 kDa
Isotype: IgG
Immunogen: Synthetic peptide within Human HDAC9 aa 1-50 / 1,011.
Positive control: RD cell lysate, K-562 cell lysate, K-562, A431, human brain tissue, human bladder cancer tissue.
Subcellular location: Nucleus.
Recommended Dilutions:
  WB
  IF-Cell
  IF-Tissue
  IHC-P
  IP

1:2,000
1:50-1:200
1:50-1:200
1:500-1:2,000
Use at an assay dependent concentration.
Uniprot #: SwissProt: Q9UKV0 Human
Alternative names: HD 7 HD 7B HD 9 HD7 HD7B HD9 HDAC 7 HDAC 7B HDAC 9 HDAC 9B HDAC 9FL HDAC HDAC7 HDAC7B HDAC9 HDAC9_HUMAN HDAC9B HDAC9FL HDRP Histone deacetylase 4/5 related protein Histone deacetylase 7 Histone deacetylase 7B Histone deacetylase 9 Histone deacetylase 9A Histone deacetylase related protein Histone deacetylase-related protein KIAA0744 MEF2 interacting transcription repressor MITR MEF2 interacting transcription repressor protein MEF2-interacting transcription repressor MITR MITR
Images
ET1706-36_1.jpg Fig1: Western blot analysis of HDAC9 on different lysates with Rabbit anti-HDAC9 antibody (ET1706-36) at 1/2,000 dilution.

Lane 1: RD cell lysate
Lane 2: K-562 cell lysate

Lysates/proteins at 20 µg/Lane.

Predicted band size: 111 kDa
Observed band size: 160 kDa

Exposure time: 1 minute 18 seconds; ECL: K1802;

4-20% SDS-PAGE gel.

Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (ET1706-36) at 1/2,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.
ET1706-36_2.jpg Fig2: Immunocytochemistry analysis of K-562 cells labeling HDAC9 with Rabbit anti-HDAC9 antibody (ET1706-36) at 1/100 dilution.

Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-HDAC9 antibody (ET1706-36) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.
ET1706-36_3.jpg Fig3: ICC staining of HDAC9 in A431 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1706-36, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).
ET1706-36_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded human brain tissue with Rabbit anti-HDAC9 antibody (ET1706-36) at 1/2,000 dilution.

The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 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 (ET1706-36) at 1/2,000 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.
ET1706-36_5.jpg Fig5: Immunohistochemical analysis of paraffin-embedded human bladder cancer tissue with Rabbit anti-HDAC9 antibody (ET1706-36) at 1/500 dilution.

The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 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 (ET1706-36) at 1/500 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.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.