DUSP6 Recombinant Rabbit Monoclonal Antibody [SR39-09]
cat.: ET1602-18
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IF-Tissue, IHC-P, IP
Clonality: Monoclonal
Clone number: SR39-09
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: 42 kDa
Isotype: IgG
Immunogen: Recombinant protein within Human DUSP6 aa 325-381 / 381.
Positive control: HepG2 cell lysate, RAW264.7 cell lysate, C6 cell lysate, Human lung tissue lysate, Mouse brain tissue lysate, Rat brain tissue lysate, human pancreas tissue, mouse pancreas tissue, human gastric carcinoma tissue, mouse brain tissue.
Subcellular location: Cytoplasm.
Recommended Dilutions:
  WB
  IF-Tissue
  IHC-P
  IP

1:1,000
1:50
1:200-1:1,000
Use at an assay dependent concentration.
Uniprot #: SwissProt: Q16828 Human | Q9DBB1 Mouse | Q64346 Rat
Alternative names: Dual specificity phosphatase 6 Dual specificity phosphatase 6 isoform a Dual specificity protein phosphatase 6 Dual specificity protein phosphatase PYST1 DUS6_HUMAN DUSP 6 DUSP 6a Dusp6 DUSP6a HH19 MAP kinase phosphatase 3 Mitogen activated protein kinase phosphatase 3 Mitogen-activated protein kinase phosphatase 3 MKP 3 MKP-3 MKP3 PYST 1 PYST1 Serine/threonine specific protein phosphatase
Images
ET1602-18_1.jpg Fig1: Western blot analysis of DUSP6 on different lysates with Rabbit anti-DUSP6 antibody (ET1602-18) at 1/1,000 dilution.

Lane 1: HepG2 cell lysate
Lane 2: RAW264.7 cell lysate
Lane 3: C6 cell lysate
Lane 4: Human lung tissue lysate
Lane 5: Mouse brain tissue lysate
Lane 6: Rat brain tissue lysate

Lysates/proteins at 20 µg/Lane.

Predicted band size: 42 kDa
Observed band size: 40 kDa

Exposure time: 1 minute; ECL: K1801;

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 (ET1602-18) at 1/1,000 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.
ET1602-18_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human pancreas tissue with Rabbit anti-DUSP6 antibody (ET1602-18) at 1/200 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 (ET1602-18) at 1/200 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.
ET1602-18_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded mouse pancreas tissue with Rabbit anti-DUSP6 antibody (ET1602-18) at 1/200 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 (ET1602-18) at 1/200 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.
ET1602-18_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded human gastric carcinoma tissue using anti-DUSP6 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 (ET1602-18, 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.
ET1602-18_5.jpg Fig5: Immunohistochemical analysis of paraffin-embedded mouse brain tissue using anti-DUSP6 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 (ET1602-18, 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”.