ERAS Mouse Monoclonal Antibody [D10-B9]
cat.: M1505-1
Product Type: Mouse monoclonal IgG1, primary antibodies
Species reactivity: Human, Mouse
Applications: IF-Cell, IHC-P
Clonality: Monoclonal
Clone number: D10-B9
Form: Liquid
Storage condition: Shipped at 4℃. Store at +4℃ short term (1-2 weeks). It is recommended to aliquot into single-use upon delivery. Store at -20℃ long term.
Storage buffer: 1*PBS (pH7.4), 0.2% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 2ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 25 kDa
Isotype: IgG1
Immunogen: Recombinant protein within Human ERAS aa 1-233 / 233.
Positive control: Human colon cancer tissue, human brain tissue, mouse brain tissue, NCCIT.
Subcellular location: Cell membrane.
Recommended Dilutions:
  IF-Cell
  IHC-P

1:50
1:200-1:1,000
Uniprot #: SwissProt: Q7Z444 Human | Q7TN89 Mouse
Alternative names: E ras E-Ras ecat5 Embryonic stem cell expressed Ras Embryonic stem cell-expressed Ras Eras ES cell expressed Ras GTPase ERas Ha-Ras2 HRAS2 HRASP MGC126691 MGC126693 OTTHUMP00000065857 RASE_HUMAN Small GTPase protein E Ras v Ha ras Harvey rat sarcoma viral oncogene homolog pseudogene v Ha ras Harvey rat sarcoma viral oncogene homolog 2
Images
M1505-1_1.jpg Fig1: Immunohistochemical analysis of paraffin-embedded human colon cancer tissue with Rabbit anti-ERAS antibody (M1505-1) 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 (M1505-1) 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.
M1505-1_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human brain tissue with Rabbit anti-ERAS antibody (M1505-1) 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 (M1505-1) 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.
M1505-1_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded mouse brain tissue with Rabbit anti-ERAS antibody (M1505-1) 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 (M1505-1) 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.
M1505-1_4.jpg Fig4: ICC staining ERAS in NCCIT 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 ERAS monoclonal antibody at a dilution of 1:50 for 1 hour at room temperature, washed with PBS. Alexa Fluorc™ 488 Goat anti-Mouse IgG was used as the secondary antibody at 1/100 dilution.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.