F4/80 Recombinant Antibody [PSH0-85] - Rat IgG1 (Chimeric) - BSA and Azide free
cat.: HA610319
Product Type: Recombinant Chimeric Antibody, primary antibodies
Species reactivity: Mouse, Rat
Applications: IHC-P
Clone number: PSH0-85
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*PBS (pH7.4).
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 102 kDa
Immunogen: Recombinant protein within mouse F4/80 aa 1-650 / 931.
Positive control: Mouse liver tissue, rat liver tissue.
Subcellular location: Cell membrane.
Recommended Dilutions:
  IHC-P

1:1,000
Uniprot #: SwissProt: Q61549 Mouse | Q5Y4N8 Rat
Alternative names: ADGRE1 Adhesion G protein coupled receptor E1 Adhesion G protein-coupled receptor E1 AGRE1_HUMAN Cell surface glycoprotein EMR1 Cell surface glycoprotein F4/80 DD7A5 7 Egf like module containing mucin like hormone receptor like 1 Egf like module containing mucin like hormone receptor like sequence 1 EGF like module receptor 1 EGF TM7 EGF-like module receptor 1 EGF-like module-containing mucin-like hormone receptor-like 1 EGFTM7 EMR 1 EMR1 EMR1 hormone receptor Gpf480 Ly71 Lymphocyte antigen 71 TM7LN3
Images
HA610319_1.jpg Fig1: Immunohistochemical analysis of paraffin-embedded mouse liver tissue with Rat anti-F4/80 antibody (HA610319) 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 (HA610319) 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.
HA610319_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded rat liver tissue with Rat anti-F4/80 antibody (HA610319) 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 (HA610319) 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”.