KRAS Mouse Monoclonal Antibody [A8E4]
cat.: HA601058
Product Type: Mouse monoclonal IgG2b, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IF-Cell, FC
Clonality: Monoclonal
Clone number: A8E4
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: 21 kDa
Isotype: IgG2b
Immunogen: Recombinant protein within human KRAS aa 2-186.
Positive control: Rat brain tissue lysate, Jurkat cell lysate, N2A cell lysate, PC-12 cell lysate, human kidney tissue lysate, Hela, NIH/3T3.
Subcellular location: Cell membrane. Cytoplasm.
Recommended Dilutions:
  WB
  IF-Cell
  FC

1:500-1:1,000
1:200
1:500-1:1,000
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
HA601058_1.jpg Fig1: Western blot analysis of KRAS on different lysates with Mouse anti-KRAS antibody (HA601058) at 1/500 dilution.

Lane 1: Rat brain tissue lysate (20 µg/Lane)
Lane 2: Jurkat cell lysate (10 µg/Lane)
Lane 3: N2A cell lysate (10 µg/Lane)

Predicted band size: 21 kDa
Observed band size: 21 kDa

Exposure time: 2 minutes;

15% 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 (HA601058) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody (HA1006) at 1:100,000 dilution was used for 1 hour at room temperature.
HA601058_2.jpg Fig2: Western blot analysis of KRAS on different lysates with Mouse anti-KRAS antibody (HA601058) at 1/1,000 dilution.

Lane 1: PC-12 cell lysate (10 µg/Lane)
Lane 2: Human kidney tissue lysate (20 µg/Lane)

Predicted band size: 21 kDa
Observed band size: 21 kDa

Exposure time: 2 minutes;

15% 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 (HA601058) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody (HA1006) at 1:100,000 dilution was used for 1 hour at room temperature.
HA601058_3.jpg Fig3: Immunocytochemistry analysis of Hela cells labeling KRAS with Mouse anti-KRAS antibody (HA601058) at 1/200 dilution.

Cells were fixed in 4% paraformaldehyde for 30 minutes, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes, and then blocked with 2% BSA for 30 minutes at room temperature. Cells were then incubated with Mouse anti-KRAS antibody (HA601058) at 1/200 dilution in 2% BSA overnight at 4 ℃. Goat Anti-Mouse IgG H&L (iFluor™ 488, HA1125) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.
HA601058_4.jpg Fig4: Flow cytometric analysis of NIH/3T3 cells labeling KRAS.

Cells were fixed and permeabilized, and then blocked with 2% negative goat serum for 15 minutes at room temperature.Then stained with the primary antibody (HA601058, 1ug/ml) (red) compared with Mouse IgG1 Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Mouse IgG Secondary antibody (HA1125) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.