KRAS Mouse Monoclonal Antibody [A8E6]
cat.: HA601060
Product Type: Mouse monoclonal IgG1, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IHC-P
Clonality: Monoclonal
Clone number: A8E6
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: PBS (pH7.4), 0.1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 22 kDa
Isotype: IgG1
Immunogen: Recombinant protein within human KRAS aa 2-186.
Positive control: HEK-293 cell lysate, 22RV1 cell lysate, mouse brain tissue lysate, mouse kidney tissue lysate, rat brain tissue lysate, mouse colon tissue, mouse kidney tissue, rat colon tissue.
Subcellular location: Cell membrane. Cytoplasm.
Recommended Dilutions:
  WB
  IHC-P

1:500-1:2,000
1:1,000
Uniprot #: SwissProt: P01116 Human | P32883 Mouse | P08644 Rat
Alternative names: c Ki ras2 c Kirsten ras protein c-K-ras c-Ki-ras Cellular c Ki ras2 proto oncogene Cellular transforming proto oncogene CFC2 cK Ras GTPase KRas K RAS p21 protein K RAS2A K RAS2B K RAS4A K RAS4B K-Ras 2 KI RAS Ki-Ras KIRSTEN MURINE SARCOMA VIRUS 2 Kirsten rat sarcoma 2 viral (v Ki ras2) oncogene homolog Kirsten rat sarcoma viral oncogene homolog KRAS KRAS proto oncogene, GTPase KRAS1 KRAS2 N-terminally processed NS NS3 Oncogene KRAS2 p21ras PR310 c K ras oncogene PR310 cK ras oncogene RALD RASK_HUMAN RASK2 Transforming protein p21 v Ki ras2 Kirsten rat sarcoma 2 viral oncogene homolog v Ki ras2 Kirsten rat sarcoma viral oncogene homolog
Images
HA601060_1.jpg Fig1: Western blot analysis of KRAS on different lysates with Mouse anti-KRAS antibody (HA601060) at 1/2,000 dilution.

Lane 1: HEK-293 cell lysate
Lane 2: 22RV1 cell lysate
Lane 3: Mouse brain tissue lysate
Lane 4: Mouse kidney tissue lysate
Lane 5: Rat brain tissue lysate

Lysates/proteins at 30 µg/Lane.

Predicted band size: 22 kDa
Observed band size: 22 kDa

Exposure time: 43 seconds;

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 (HA601060) at 1/2,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Anti-Mouse IgG for IP Nano-secondary antibody (NBI02H) at 1/5,000 dilution was used for 1 hour at room temperature.
HA601060_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded mouse colon tissue with Mouse anti-KRAS antibody (HA601060) 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 (HA601060) 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.
HA601060_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded mouse kidney tissue with Mouse anti-KRAS antibody (HA601060) 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 (HA601060) 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.
HA601060_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded rat colon tissue with Mouse anti-KRAS antibody (HA601060) 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 (HA601060) 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”.