Midkine Recombinant Rabbit Monoclonal Antibody [JF096-5]
cat.: ET1702-64
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human
Applications: WB, IHC-P, IP
Clonality: Monoclonal
Clone number: JF096-5
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: 16 kDa
Isotype: IgG
Immunogen: Synthetic peptide within Human Midkine aa 100-143 / 143.
Positive control: Human liver carcinoma tissue, human pancreas tissue.
Subcellular location: Secreted.
Recommended Dilutions:
  WB
  IHC-P

1:500-1:1,000
1:1,000
Uniprot #: SwissProt: P21741 Human
Alternative names: Amphiregulin associated protein Amphiregulin-associated protein ARAP FLJ27379 Mdk Midgestation and kidney protein Midkine MK 1 MK MK_HUMAN MK1 NEGF 2 NEGF2 Neurite growth promoting factor 2 Neurite outgrowth promoting protein Neurite outgrowth-promoting factor 2 Neurite outgrowth-promoting protein Retinoic acid inducible factor
Images
ET1702-64_1.jpg Fig1: Immunohistochemical analysis of paraffin-embedded human liver tissue with Rabbit anti-Midkine antibody (ET1702-64) at 1/1,000 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 (ET1702-64) at 1/1,000 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.
ET1702-64_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human pancreas tissue with Rabbit anti-Midkine antibody (ET1702-64) at 1/1,000 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 (ET1702-64) at 1/1,000 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.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.